Causes of Jaundice
List of causes of Jaundice
Following is a list of causes or underlying conditions
(see also Misdiagnosis of underlying causes of Jaundice)
that could possibly cause Jaundice includes:
- Neonatal jaundice - common type in newly born babies.
- Liver diseases
- Causes of hemolytic jaundice:
- Causes of obstruction jaundice:
- Pernicious anemia
- Stomach cancer
- Secondary liver cancer (type of Liver cancer)
- Pancreatic cancer
- Typhoid fever
- Yellow fever
- Leptospirosis
- Snake venom
- Q fever - jaundice
- Xanthogranulomatous cholecystitis - Jaundice
- Warm Autoimmune Hemolytic Anemia - jaundice
- Triosephosphate isomerase 1 - jaundice
- Toxic mushrooms - Monomethylhydrazine - jaundice
- Septo-Optic Dysplasia - jaundice
- PFIC - jaundice
- Occupational metal-induced liver damage - Germanium - jaundice
- Occupational liver damage - Acetates - jaundice
- Liver cancer - jaundice
- Inherited spherocytic anemia - jaundice
- Hepatoma - jaundice
- Hemophagocytic lymphohistiocytosis, familial, 3 - jaundice
- Galactosemia III - jaundice
- Galactokinase deficiency - jaundice
- Endocrine agent-induced liver damage - Oral hypoglycemics - jaundice
- Drugs-induced liver damage - Ether - jaundice
- Drug-induced liver damage - Dantrolene - jaundice
- Drug-induced Immune Hemolytic Anemia - jaundice
- Congenital tuberculosis - jaundice
- Congenital spherocytic hemolytic anemia - jaundice
- Chemical poisoning - Chloromethane - jaundice
- Antiprotozoal agent-induced liver damage - 8-Hydroxyquinolone - jaundice
- Antimetazoal agent-induced liver damage - jaundice
- Antifungal agent-induced liver damage - Amphotericin - jaundice
- Antibiotics-induced liver damage - Spectinomycin - jaundice
- Anesthetic agent-induced liver damage - Cyclopropane - jaundice
- Acral dysostosis - dyserythropoiesis - jaundice
- Surgical shunt to reduce portal hypertension
- Hepatic abscess
- Heart failure
- Dubin-Johnson syndrome
- Alcoholic liver disease - jaundice
- Acute liver damage (see Liver damage)
- Reticulo-endothelial malignancy
- Pyruvate kinase deficiency - jaundice
- Crigler-Najjar syndrome - jaundice
- Rotor's syndrome
- Hepatic cirrhosis
- Pulmonary infarction
- Hepatitis C and B
- Thyroid agenesis - jaundice
- Spherocytic anemia - jaundice
- Secondary Cold Autoimmune Hemolytic Anemia - jaundice
- Secondary Autoimmune Hemolytic Anemia - jaundice
- Psychotropic agent-induced liver damage - Thioxanthene - jaundice
- Primary sclerosing cholangitis - jaundice
- Plant toxin-induced liver damage - Ngaione - jaundice
- Organic acidemia - jaundice
- Meningitis - Jaundice
- Marburg virus - jaundice
- Leiomyosarcoma - jaundice
- Inborn amino acid metabolism disorder - jaundice
- Hydatidosis - jaundice
- Horse nettle poisoning - jaundice
- Herbal Agent adverse reaction - Chaparral - jaundice
- Hemophagocytic lymphohistiocytosis, familial, 4 - jaundice
- Cold Autoimmune Hemolytic Anemia - jaundice
- Blueberry muffin syndrome - jaundice
- Autoimmune Hemolytic Anemia - jaundice
- Antituberculous agent-induced liver damage - Ethionamide - jaundice
- Anticonvulsive-induced liver damage - Mephenytoin - jaundice
- Hepatic cancer
- Carcinoma of the ampulla
- Congenital obliteration of the bile duct
- Aminata wild mushrooms
- Appendicitis
- Mismatched blood transfusion
- Enzyme defects
- Drug induced liver disease( amiodarone, alpha methyldopa, methotrexate)
- Spleen Cancer - jaundice
- Pseudo-torch syndrome - jaundice
- Penicillin-induced Immune Hemolytic Anemia - jaundice
- Pancreatic Islet Cell Cancer - Jaundice
- Lymphoma - jaundice
- Hereditary spherocytic hemolytic anemia - jaundice
- Hepatic Venoocclusive Disease with immunodeficiency - jaundice
- Hemolytic disease of the newborn - jaundice
- Griscelli syndrome type II - jaundice
- Cytomegalic Inclusion Body Disease - Jaundice
- Copper toxicity - jaundice
- Congenital herpes simplex - jaundice
- Breast Milk Jaundice - jaundice
- Bile acid synthesis defect, congenital, 2 - jaundice
- Benign intrahepatic cholestasis type 1 - jaundice
- Acute pancreatitis
- Heamochromatosis
- Carbon tetrachloride
- Yellow fever virus
- Liver tumor
- Disseminated lupus erythematosus
- Biliary obstruction
- Medications
- Right heart failure
- Vitamin C Overdose - jaundice
- Spleen neoplasm - jaundice
- Rhabdomyosarcoma, embryonal - jaundice
- Primary Cold Autoimmune Hemolytic Anemia - jaundice
- Primary Autoimmune Hemolytic Anemia - jaundice
- Neuroma biliary tract - jaundice
- Mycotoxin-induced liver damage - Sterigmatocystin - jaundice
- Mononucleosis - jaundice
- Malignant Buotonneuse fever - jaundice
- Hereditary non-spherocytic hemolytic anemia - jaundice
- Hepatitis X (non-A,-B,-C,-D,-E) - jaundice
- Endocrine pancreatic cancer - Jaundice
- Cooley syndrome - jaundice
- Congenital disorder of glycosylation type 1H - jaundice
- Beta thalassemia - jaundice
- Benign intrahepatic cholestasis type 2 - jaundice
- Anemia - jaundice
- Alagille Syndrome - jaundice
- Acinic cell carcinoma - jaundice
- Reye's syndrome
- Cytomegalovirus disease
- Retroperitoneal cyst
- Recurrent idiopathic cholestasis
- Cardiac failure
- Acute fatty liver of pregnancy - jaundice
- Reticuloendothelial tumor
- Gangrene
- Sickle-cell disease
- Elliptocytosis
- Sepsis - Jaundice
- Biliary cirrhosis
- Gilbert's syndrome
- Pancreatic adenoma - jaundice
- X-linked sideroblastic anemia - jaundice
- Warm-reacting-antibody haemolytic anemia - Jaundice
- Viral meningitis - Jaundice
- UDP-Galactose-4-epimerase deficiency - Jaundice
- Quinidine-induced Immune Hemolytic Anemia - jaundice
- Pancreatoblastoma - jaundice
- Niemann-Pick disease, type A - jaundice
- Neonatal bacterial meningitis - jaundice
- Myelofibrosis-osteosclerosis - jaundice
- Lissencephaly syndrome type 1 - jaundice
- Goldstein-Hutt syndrome - jaundice
- Glutaricaciduria 2B - jaundice
- Choledochal cyst, hand malformation - jaundice
- Babesiosis - Jaundice
- Abdominal Cancer - jaundice
- Abdominal surgery (see Abdominal symptoms)
- Peritoneal adhesion
- Parasites
- Alpha-1 antitrypsin deficiency - jaundice
- Galactosemia - Jaundice
- Dicophane
- Paroxysmal nocturnal hemoglobinuria
- Industrial toxins
- Wilson disease
- X-linked lymphoproliferative syndrome - Jaundice
- Wyatt disease - jaundice
- Thrombotic thrombocytopenic purpura, acquired - jaundice
- Porphyria, congenital erythropoietic - chronic jaundice
- Pancreatic islet cell tumors (non-functioning tumor) - jaundice
- Metabolic disorders - Jaundice
- Hodgkin's Disease - jaundice
- Herbal Agent overdose - Psoralea Corylifolia - jaundice
- Hepatotoxicity - jaundice
- Hashimoto-Pritzker syndrome - jaundice
- Graft-versus-host disease - Jaundice
- Gall bladder conditions - Jaundice
- Crigler-Najjar syndrome, type 2 - jaundice
- Congenital spherocytic anemia - jaundice
- Congenital malaria - jaundice
- Classic galactosemia - jaundice
- Black nightshade poisoning - jaundice
- Beta Thalassemia intermedia - jaundice
- Antiviral agent-induced liver damage - xenylamine - jaundice
- Angiosarcoma of the liver - jaundice
- Alpha thalassemia - jaundice
- Acute liver failure - jaundice
- Congenital dyserythropoietic anaemia type 1
- Kawasaki disease - jaundice
- Chronic pancreatitis
- Primary biliary cirrhosis - jaundice
- Trinitrotoluene
- Relapsing fever - jaundice
- Excessive exercise (see Exercise symptoms)
- Severe burns (type of Burns)
- Hemoglobinopathy
- Carotenemia
- Choledocholithiasis
- Xerocytosis, heriditary - Jaundice
- X-linked alpha thalassemia mental retardation syndrome (ATR-X) - Jaundice
- Warm-reacting-antibody hemolytic anemia - jaundice
- TORCH Syndrome - jaundice
- Summerskill-Walshe-Tygstrup syndrome - jaundice
- Sulfone syndrome - jaundice
- Rh Disease - jaundice
- Pyruvate kinase deficiency, liver type - jaundice
- Pancreatic carcinoma, familial - jaundice
- Non functioning pancreatic endocrine tumor - jaundice
- NISCH syndrome - jaundice
- Neonatal sepsis - jaundice
- Neonatal hepatitis - jaundice
- Malignant obstructive biliary disease - jaundice
- Kaposiform hemangio-endothelioma - jaundice
- Itraconazole toxicity - jaundice
- Hepatic encephalopathy syndrome - jaundice
- Hemoglobin C homozygous (CC) - jaundice
- HELLP syndrome - jaundice
- Distomatosis - jaundice
- Bile plug syndrome - jaundice
- Bile acid synthesis defects, congenital, 1 - jaundice
- Anemia, Neonatal - jaundice
- Adrenal hemorrhage, neonatal - jaundice
- Absence of septum pellucidum and septo-optic dysplasia - jaundice
- Carbimazole
- Methimazole
- Hydatid cyst
- Rotor syndrome
- Budd-Chiari syndrome - jaundice
- Cytomegalovirus
- Rubella
- HbSC disease
- Infectious mononucleosis
- Reticuloendotheliosis - jaundice
- Niemann-Pick disease - jaundice
- Methyldopa-induced Immune Hemolytic Anemia - jaundice
- Metal-induced liver damage - jaundice
- Lambert syndrome - jaundice
- Gold poisoning - jaundice
- Cholestasis - jaundice
- Cholangitis - jaundice
- Biliary tract cancer - jaundice
- Bile duct cancer, extrahepatic - jaundice
- Bile acid synthesis defects, congenital, 2 - jaundice
- Achrestic anemia - jaundice
- Cholecystitis - jaundice
- Mirizzi's syndrome
- Constrictive pericarditis
- HCV viral infection
- Infectious hepatitus
- Coxsackie B
- Viral pneumonia (type of Pneumonia)
- Thalassaemia
- Infective endocarditis - jaundice
- Bacterial endocarditis - jaundice
- Transfusion Reaction - Jaundice
- Sulphonamide -induced Immune Hemolytic Anemia - jaundice
- Soto's Syndrome - jaundice
- Sarcoma botryoides - jaundice
- Rhabdomyosarcoma, embryonal 1 - jaundice
- Rh deficiency syndrome - jaundice
- Percocet overdose - jaundice
- Pancreatic cancer, adult - jaundice
- Obstructive biliary disease - jaundice
- Non-hereditary spherocytic anemia - jaundice
- Malignant Jaundice - jaundice
- Intrahepatic cholangiocarcinoma - jaundice
- Hepatic amyloidosis with intrahepatic cholestasis - jaundice
- Hanot-MacMahon-Thannhauser syndrome - jaundice
- Favism - jaundice
- Fanconi-ichthyosis-dysmorphism - jaundice
- Eclampsia - jaundice
- Doxepine-induced Immune Hemolytic Anemia - jaundice
- Deal-Barratt-Dillon syndrome - jaundice
- Congenital Toxoplasmosis - jaundice
- Chronic Hepatitis C - Jaundice
- Cholestatic jaundice -renal tubular insufficiency - jaundice
- Cholestasis, progressive familial intrahepatic 1 - jaundice
- Cephalosporin-induced Immune Hemolytic Anemia - jaundice
- Cardiomyopathy - spherocytosis - jaundice
- Bile acid synthesis defects, congenital, 3 - jaundice
- Bile acid synthesis defects - jaundice
- Baber's syndrome - jaundice
- Alpha thalassemia major - jaundice
- Aldolase A deficiency - jaundice
- Aagenaes syndrome - jaundice
- Rh problems
- Cholelithiasis
- Duodenal diverticulum
- Biliary atresia - jaundice
- Congenital hepatic fibrosis
- Cold hemoglobinuria
- Haemolysis
- Hematoma
- Glycogen storage disorder
- Cirrhosis, familial - jaundice
- Zieve syndrome - jaundice
- Vitamin B12 Deficiency - jaundice
- Thalassemia - jaundice
- Rhabdomyosarcoma, embryonal 2 - jaundice
- Pyruvate kinase deficiency, hemolytic anemia - jaundice
- Postoperative Jaundice - jaundice
- Phenothiazine antenatal infection - jaundice
- Langerhans Cell Histiocytosis - jaundice
- Hereditary elliptocytosis - jaundice
- Hepatic veno-occlusive disease - immunodeficiency - jaundice
- Hemophagocytic lymphohistiocytosis, familial, 1 - jaundice
- Griscelli disease - jaundice
- Fructose-1-phosphate aldolase deficiency, hereditary - jaundice
- Fascioliasis - jaundice
- Congenital syphilis - jaundice
- Cold antibody hemolytic anemia - jaundice
- Chromosome 18, trisomy 18q - jaundice
- Cholestasis, progressive familial intrahepatic 2 - jaundice
- Cholestasis, Intrahepatic - jaundice
- Childhood liver cancer, primary - jaundice
- Bile acid synthesis defects, congenital, 4 - jaundice
- Bernard syndrome - jaundice
- Arthrogryposis - renal dysfunction - cholestasis syndrome - jaundice
- Anemic - hematuria syndrome - jaundice
- Addison-Gull syndrome - chronic jaundice
- Acute Cholecystitis - jaundice
- Acanthocytosis - jaundice
- Mianserin
- Sickle cell anemia - jaundice
- Bile duct trauma
- Enlarged portal lymph nodes
- Carcinoma of the bile duct
- Long-standing extrahepatic biliary obstruction
- Glycogen storage diseases
- Serum hepatitis
- Herpes simplex
- Amyloidosis
- Poisons
- Leukemia
- Spherocytosis
- Biliary duct carcinoma
- Brown Recluse spider poisoning - jaundice
- Zellweger Syndrome - Jaundice
- Thrombotic thrombocytopenic purpura, congenital - jaundice
- Sickle cell crisis - jaundice
- Pyruvate kinase deficiency, muscle type - jaundice
- Lissencephaly - jaundice
- Irish potato poisoning - jaundice
- Histiocytosis, Non-Langerhans-Cell - jaundice
- Herpes, Neonatal - Disseminated - jaundice
- Hepatorenal tyrosinemia - jaundice
- Hemophagocytic lymphohistiocytosis, familial, 2 - jaundice
- Galactosemia I - jaundice
- End Stage Liver Failure - jaundice
- Congenital nonhemolytic jaundice - jaundice
- Congenital cytomegalovirus - jaundice
- Cholestasis, progressive familial intrahepatic 3 - jaundice
- Alveolar Hydatid Disease - jaundice
- Abdominal Neoplasms - jaundice
- Ineffective erythropoiesis
- Cancer of the ampulla of Vater
- Aneurysm of the hepatic artery
- Pregnancy
- Sclerosing cholangitis
- Wilson's disease - jaundice
- HBV liver infection
- Sarcoidosis
- Glucose-6-phosphate dehydrogenase deficiency
- Autoimmune hemolytic anaemia
- Lucey-Driscoll syndrome
- Gilbert's disease
- Hemolysis
More causes:
see full list of causes for Jaundice
Causes of Jaundice (Diseases Database):
The follow list shows some of the possible medical causes of Jaundice
that are listed by the Diseases Database:
Source: Diseases Database
Jaundice Causes: Book Excerpts
Jaundice as a complication of other conditions:
Other conditions that might have
Jaundice as a complication may,
potentially, be an underlying cause of Jaundice.
Our database lists the following as having
Jaundice as a complication of that condition:
Jaundice as a symptom:
Conditions listing Jaundice
as a symptom may also be potential underlying causes of Jaundice.
Our database lists the following as having
Jaundice as a symptom of that condition:
- Aagenaes syndrome
- Abdominal Cancer
- Abdominal Neoplasms
- Absence of septum pellucidum and septo-optic dysplasia
- Acanthocytosis
- Achrestic anemia
- Acinic cell carcinoma
- Acral dysostosis - dyserythropoiesis
- Acute Cholecystitis
- Acute fatty liver of pregnancy
- Acute liver failure
- Acute meningitis
- Adrenal hemorrhage, neonatal
- Alagille Syndrome
- Alcoholic liver disease
- Aldolase A deficiency
- Alpha 1-Antitrypsin Deficiency
- Alpha thalassemia
- Alpha thalassemia - Hemoglobin H disease
- Alpha thalassemia major
- Alveolar Hydatid Disease
- Anemia
- Anemia, Hemolytic, Warm Antibody
- Anemia, Neonatal
- Anemic - hematuria syndrome
- Anesthetic agent-induced liver damage
- Anesthetic agent-induced liver damage - Chloroform
- Anesthetic agent-induced liver damage - Cyclopropane
- Anesthetic agent-induced liver damage - Ether
- Anesthetic agent-induced liver damage - Halothane
- Anesthetic agent-induced liver damage - Methoxyflurane
- Anesthetic agent-induced liver damage - Nitrous Oxide
- Angiosarcoma of the liver
- Antibiotics-induced liver damage
- Antibiotics-induced liver damage - Cephalosporin
- Antibiotics-induced liver damage - Chloramphenicol
- Antibiotics-induced liver damage - Clindamycin
- Antibiotics-induced liver damage - Erythromycin estolate
- Antibiotics-induced liver damage - Erythromycin Ethyl succinate
- Antibiotics-induced liver damage - Novobiocin
- Antibiotics-induced liver damage - Quinolone
- Antibiotics-induced liver damage - Spectinomycin
- Antibiotics-induced liver damage - Sulfones
- Antibiotics-induced liver damage - Telithromycin
- Antibiotics-induced liver damage - Tetracycline
- Antibiotics-induced liver damage - Nitrofuran
- Antibiotics-induced liver damage - Penicillin
- Antibiotics-induced liver damage - Rifampicin
- Anticonvulsive-induced liver damage
- Anticonvulsive-induced liver damage - Mephenytoin
- Anticonvulsive-induced liver damage - Phenobarbital
- Anticonvulsive-induced liver damage - Phenytoin
- Anticonvulsive-induced liver damage - Valproic Acid
- Antifungal agent-induced liver damage
- Antifungal agent-induced liver damage - 5-Fluorocytosine
- Antifungal agent-induced liver damage - Amphotericin
- Antifungal agent-induced liver damage - Griseofulvin
- Antifungal agent-induced liver damage - Ketoconazole
- Antifungal agent-induced liver damage - Saramycetin
- Antimetazoal agent-induced liver damage
- Antimetazoal agent-induced liver damage - Amodiaquine
- Antimetazoal agent-induced liver damage - Hycanthone
- Antiprotozoal agent-induced liver damage
- Antiprotozoal agent-induced liver damage - 8-Hydroxyquinolone
- Antiprotozoal agent-induced liver damage - Carbarsone
- Antiprotozoal agent-induced liver damage - Emetine
- Antiprotozoal agent-induced liver damage - Mepacrine
- Antiprotozoal agent-induced liver damage - Metronidazole
- Antiprotozoal agent-induced liver damage - Thiabendazole
- Antituberculous agent-induced liver damage
- Antituberculous agent-induced liver damage - Cycloserine
- Antituberculous agent-induced liver damage - Ethionamide
- Antituberculous agent-induced liver damage - Isoniazid
- Antituberculous agent-induced liver damage - p-aminosalicylic acid
- Antituberculous agent-induced liver damage - Rifampicin
- Antiviral agent-induced liver damage
- Antiviral agent-induced liver damage - Cytarabine
- Antiviral agent-induced liver damage - idoxuridine
- Antiviral agent-induced liver damage - Vidarabine
- Antiviral agent-induced liver damage - xenylamine
- Arthrogryposis - renal dysfunction - cholestasis syndrome
- Autoimmune Hemolytic Anemia
- Autoimmune Hepatitis
- Baber's syndrome
- Babesiosis
- Bacterial meningitis
- Benign intrahepatic cholestasis type 1
- Benign intrahepatic cholestasis type 2
- Bernard syndrome
- Beta thalassemia
- Beta Thalassemia intermedia
- Bile acid synthesis defect, congenital, 2
- Bile acid synthesis defect, congenital, 4
- Bile acid synthesis defects
- Bile acid synthesis defects, congenital, 1
- Bile acid synthesis defects, congenital, 2
- Bile acid synthesis defects, congenital, 3
- Bile acid synthesis defects, congenital, 4
- Bile duct cancer, extrahepatic
- Bile duct paucity in Graft-Versus-Host Disease
- Bile duct paucity in Liver Allograft Rejection
- Bile duct paucity, non syndromic form
- Bile plug syndrome
- Biliary Atresia
- Biliary cirrhosis
- Biliary tract cancer
- Black nightshade poisoning
- Blueberry muffin syndrome
- Breast Milk Jaundice
- Budd-Chiari syndrome
- Cardiomyopathy - spherocytosis
- Cephalosporin-induced Immune Hemolytic Anemia
- Chediak-Higashi like syndrome
- Chemical poisoning - 1,2-Dibromoethane
- Chemical poisoning - Acetylene Tetrabromide
- Chemical poisoning - Arsine
- Chemical poisoning - Carbon Tetrachloride
- Chemical poisoning - Chlorate salts
- Chemical poisoning - Chlorinated naphthalene
- Chemical poisoning - Chlorodiphenyl
- Chemical poisoning - Chloromethane
- Chemical poisoning - Diethylene Glycol
- Chemical poisoning - Dimethylnitrosamine
- Chemical poisoning - Dinitrocresol
- Chemical poisoning - Dinitrophenol
- Chemical poisoning - Methylene Dianiline
- Chemical poisoning - Naphthalene
- Chemical poisoning - Para-Dichlorobenzene
- Chemical poisoning - Phosphine
- Chemical poisoning - Solder
- Chemical poisoning - White Phosphorus
- Childhood liver cancer, primary
- Cholangitis
- Cholecystitis
- Choledochal cyst, hand malformation
- Cholestasis
- Cholestasis - lymphoedema, syndrome
- Cholestasis - pigmentary retinopathy - cleft palate
- Cholestasis, Intrahepatic
- Cholestasis, progressive familial intrahepatic 1
- Cholestasis, progressive familial intrahepatic 2
- Cholestasis, progressive familial intrahepatic 3
- Cholestatic jaundice -renal tubular insufficiency
- Chromosome 18, trisomy 18q
- Chronic Hepatitis
- Chronic Hepatitis C
- Cirrhosis of the liver
- Classic galactosemia
- Classical Hodgkin disease
- Cobalamin malabsorption, selective, with proteinuria
- Cold antibody hemolytic anemia
- Cold Autoimmune Hemolytic Anemia
- Congenital cytomegalovirus
- Congenital disorder of glycosylation type 1H
- Congenital herpes simplex
- Congenital malaria
- Congenital nonhemolytic jaundice
- Congenital spherocytic anemia
- Congenital spherocytic hemolytic anemia
- Congenital syphilis
- Congenital Toxoplasmosis
- Congenital tuberculosis
- Congenital Vitamin B12 Malabsorption
- Cooley syndrome
- Copper toxicity
- Crigler-Najjar Syndrome
- Crigler-Najjar syndrome, type 2
- Cytomegalic Inclusion Body Disease
- Deal-Barratt-Dillon syndrome
- Distomatosis
- Doxepine-induced Immune Hemolytic Anemia
- Drug-induced liver damage - Clindamycin
- Drug-induced liver damage - Quinolone
- Drug-induced liver damage - Spectinomycin
- Drug-induced liver damage - Sulfones
- Drug-induced Immune Hemolytic Anemia
- Drug-induced liver damage - 5-Fluorocytosine
- Drug-induced liver damage - Allopurinol
- Drug-induced liver damage - Amphotericin
- Drug-induced liver damage - Anabolic C-17
- Drug-induced liver damage - Anesthetic agent
- Drug-induced liver damage - Antianginal agents
- Drug-induced liver damage - Antiarrhythmics
- Drug-induced liver damage - Antibiotics
- Drug-induced liver damage - Anticoagulants
- Drug-induced liver damage - anticonvulsives
- Drug-induced liver damage - Antifungals
- Drug-induced liver damage - Antihyperlipidemic agents
- Drug-induced liver damage - Antihypertensives
- Drug-induced liver damage - Antineoplastic agents
- Drug-induced liver damage - Antithyroid drugs
- Drug-induced liver damage - antituberculous agents
- Drug-induced liver damage - antiviral medication
- Drug-induced liver damage - Benzodiazepine
- Drug-induced liver damage - British anti-Lewisite penicillamine
- Drug-induced liver damage - Butyrophenone
- Drug-induced liver damage - Cephalosporin
- Drug-induced liver damage - Chloramphenicol
- Drug-induced liver damage - Chloroform
- Drug-induced liver damage - Cimetidine
- Drug-induced liver damage - Colchicine
- Drug-induced liver damage - Cyclopropane
- Drug-induced liver damage - Cycloserine
- Drug-induced liver damage - Cytarabine
- Drug-induced liver damage - Dantrolene
- Drug-induced liver damage - Diflunisal
- Drug-induced liver damage - Disulfiram
- Drug-induced liver damage - Diuretic Agents
- Drug-induced liver damage - endocrine agent
- Drug-induced liver damage - Erythromycin estolate
- Drug-induced liver damage - Erythromycin ethyl succinate
- Drug-induced liver damage - Ethionamide
- Drug-induced liver damage - Fenoprofen
- Drug-induced liver damage - Glucocorticoids
- Drug-induced liver damage - Griseofulvin
- Drug-induced liver damage - Halothane
- Drug-induced liver damage - Ibuprofen
- Drug-induced liver damage - idoxuridine
- Drug-induced liver damage - Indomethacin
- Drug-induced liver damage - Iodide ion
- Drug-induced liver damage - Isoniazid
- Drug-induced liver damage - Ketoconazole
- Drug-induced liver damage - Mephenytoin
- Drug-induced liver damage - Methoxyflurane
- Drug-induced liver damage - monoamine oxidase inhibitors
- Drug-induced liver damage - Naproxen
- Drug-induced liver damage - Nitrofuran
- Drug-induced liver damage - Nitrous Oxide
- Drug-induced liver damage - Novobiocin
- Drug-induced liver damage - Oral hypoglycemics
- Drug-induced liver damage - p-aminosalicylic acid
- Drug-induced liver damage - Penicillin
- Drug-induced liver damage - Phenobarbital
- Drug-induced liver damage - Phenothiazines
- Drug-induced liver damage - Phenylbutazone
- Drug-induced liver damage - Phenytoin
- Drug-induced liver damage - psychotropic agents
- Drug-induced liver damage - Ranitidine
- Drug-induced liver damage - Rifampicin
- Drug-induced liver damage - Salicylate
- Drug-induced liver damage - Saramycetin
- Drug-induced liver damage - Steroids
- Drug-induced liver damage - Sulfonamide
- Drug-induced liver damage - Sulindac
- Drug-induced liver damage - Tamoxifen
- Drug-induced liver damage - Telithromycin
- Drug-induced liver damage - Tetracycline
- Drug-induced liver damage - Thioxanthene
- Drug-induced liver damage - Thorotrast
- Drug-induced liver damage - tricyclic antidepressant
- Drug-induced liver damage - Valproic Acid
- Drug-induced liver damage - Vidarabine
- Drug-induced liver damage - Vitamin A
- Drug-induced liver damage - xenylamine
- Drug-induced liver damage - Zoxazolamine
- Drug-induced liver disease
- Drugs-induced liver damage - Ether
- Eclampsia
- End Stage Liver Failure
- Endocrine agent-induced liver damage
- Endocrine agent-induced liver damage - Anabolic C-17
- Endocrine agent-induced liver damage - Antithyroid drugs
- Endocrine agent-induced liver damage - Glucocorticoids
- Endocrine agent-induced liver damage - Oral contraceptives
- Endocrine agent-induced liver damage - Oral hypoglycemics
- Endocrine agent-induced liver damage - Steroids
- Endocrine agent-induced liver damage - Tamoxifen
- Endocrine pancreatic cancer
- Exocrine Pancreatic Insufficiency, Dyserythropoietic Anemia, And Calvarial Hyperostosis
- Familial Selective Vitamin B12 Malabsorption
- Fanconi-ichthyosis-dysmorphism
- Fascioliasis
- Favism
- Fructose-1-phosphate aldolase deficiency, hereditary
- Galactokinase deficiency
- Galactosemia
- Galactosemia I
- Galactosemia III
- Gall Bladder Cancer
- Gall bladder conditions
- Gallstones
- Glutaric aciduria 2
- Glutaricaciduria 2B
- Gold poisoning
- Goldstein-Hutt syndrome
- Graft-versus-host disease
- Grasbeck-Imerslund Disease
- Griscelli disease
- Griscelli syndrome type II
- Gräsbeck-Imerslund disease
- Hanot-MacMahon-Thannhauser syndrome
- Hashimoto-Pritzker syndrome
- HELLP syndrome
- Hemochromatosis
- Hemoglobin C homozygous (CC)
- Hemolytic anemia
- Hemolytic disease of the newborn
- Hemophagocytic lymphohistiocytosis, familial, 1
- Hemophagocytic lymphohistiocytosis, familial, 2
- Hemophagocytic lymphohistiocytosis, familial, 3
- Hemophagocytic lymphohistiocytosis, familial, 4
- Hepatic amyloidosis with intrahepatic cholestasis
- Hepatic encephalopathy syndrome
- Hepatic veno-occlusive disease - immunodeficiency
- Hepatic Venoocclusive Disease with immunodeficiency
- Hepatitis
- Hepatitis A
- Hepatitis B
- Hepatitis C
- Hepatitis D
- Hepatitis E
- Hepatitis X
- Hepatitis X (non-A,-B,-C,-D,-E)
- Hepatoma
- Hepatorenal tyrosinemia
- Hepatotoxicity
- Heptaosplenic T-cell Lymphoma
- Herbal Agent adverse reaction - Chaparral
- Herbal Agent adverse reaction - Germander
- Herbal Agent adverse reaction - Polygonum multiflorum
- Herbal Agent overdose - Comfrey
- Herbal Agent overdose - Psoralea Corylifolia
- Hereditary elliptocytosis
- Hereditary non-spherocytic hemolytic anemia
- Hereditary spherocytic hemolytic anemia
- Hereditary spherocytosis
- Herpes, Neonatal - Disseminated
- Histiocytosis, Non-Langerhans-Cell
- Hodgkin's Disease
- Hodgkin's disease, adult
- Hodgkin's disease, childhood
- Hodgkin's disease, nodular sclerosis
- Horse nettle poisoning
- Hydatidosis
- Idiopathic liver cirrhosis
- Imerslund's Anemia
- Imerslund's Syndrome
- Imerslund-Gräsbeck syndrome
- Imerslund-Najman-Grasbeck Anemia
- Imerslund-Najman-Grasbeck Disease
- Imerslund-Najman-Grasbeck Syndrome
- Inborn amino acid metabolism disorder
- Inborn errors of thyroid hormone synthesis related to hypothyroidism
- Inherited spherocytic anemia
- Intrahepatic cholangiocarcinoma
- Irish potato poisoning
- Itraconazole toxicity
- Juvenile Megaloblastic Anemia
- Kaposiform hemangio-endothelioma
- Kawasaki disease
- Lambert syndrome
- Langerhans Cell Histiocytosis
- Leiomyosarcoma
- Leptospirosis
- Lissencephaly
- Lissencephaly syndrome type 1
- Liver cancer
- Liver failure
- Liver vein outflow obstruction
- Lymphocyte depletion Hodgkin's disease
- Lymphoma
- Malignant Buotonneuse fever
- Malignant Jaundice
- Malignant obstructive biliary disease
- Marburg virus
- Megaloblasti Anemia, 1
- Megaloblastic anemia
- Megaloblastic Anemia, Familial
- Meningitis
- Metabolic disorders
- Metal-induced liver damage
- Metastatic liver cancer
- Methyldopa-induced Immune Hemolytic Anemia
- Mixed cellularity Hodgkin's disease
- Mononucleosis
- Mosse syndrome
- Mycotoxin-induced liver damage - Aflatoxin
- Mycotoxin-induced liver damage - Cyclochlorotine
- Mycotoxin-induced liver damage - Luteoskyrins
- Mycotoxin-induced liver damage - Ochratoxin
- Mycotoxin-induced liver damage - Rubratoxin
- Mycotoxin-induced liver damage - Sterigmatocystin
- Myelofibrosis-osteosclerosis
- NASH syndrome
- Neonatal bacterial meningitis
- Neonatal hepatitis
- Neonatal sepsis
- Neuroma biliary tract
- Niemann-Pick disease
- Niemann-Pick disease, type A
- NISCH syndrome
- Nodular sclerosing Hodgkin's lymphoma
- Non functioning pancreatic endocrine tumor
- Non-hereditary spherocytic anemia
- Obstructive biliary disease
- Occupational liver damage - 1,1,1-Tetrachloroethane
- Occupational liver damage - 1,1,2-Tetrachloroethane
- Occupational liver damage - 1,2-Dibromoethane
- Occupational liver damage - 1,2-Dichloroethane
- Occupational liver damage - 2-acetylamino-fluorene
- Occupational liver damage - 2-Nitropropane
- Occupational liver damage - 3,3-Dichlorobenzidine
- Occupational liver damage - 4-Dimethylaminoazobenzene
- Occupational liver damage - Acetates
- Occupational liver damage - Acetonitrile
- Occupational liver damage - Acrylonitrile
- Occupational liver damage - Alcohol
- Occupational liver damage - Alicyclic Hydrocarbons
- Occupational liver damage - Aliphatic Amines
- Occupational liver damage - Aliphatic Hydrocarbons
- Occupational liver damage - Aliphatic hydrogenated hydrocarbons
- Occupational liver damage - Allyl alcohol
- Occupational liver damage - Amyl acetate
- Occupational liver damage - Aromatic amines
- Occupational liver damage - Aromatic halogenated hydrocarbons
- Occupational liver damage - Aromatic Hydrocarbons
- Occupational liver damage - Arsenic
- Occupational liver damage - Arsine
- Occupational liver damage - Benzene
- Occupational liver damage - Benzyl chloride
- Occupational liver damage - Beryllium
- Occupational liver damage - Beta-Propiolactone
- Occupational liver damage - Bipyridyl pesticides
- Occupational liver damage - Bismuth
- Occupational liver damage - Boron
- Occupational liver damage - Boron hydrides
- Occupational liver damage - Bromide
- Occupational liver damage - Cadmium
- Occupational liver damage - Carbolic Acids and Anhydrides
- Occupational liver damage - Carbon Disulfide
- Occupational liver damage - Carbon tetrachloride
- Occupational liver damage - Carbonyls (metal)
- Occupational liver damage - Chlorinated benzenes
- Occupational liver damage - Chlorinated naphthalenes
- Occupational liver damage - Chlorodiphenyls and derivatives
- Occupational liver damage - Chloroform
- Occupational liver damage - Chloroprene
- Occupational liver damage - Chromium
- Occupational liver damage - Copper
- Occupational liver damage - Cresol
- Occupational liver damage - Cyclopropane
- Occupational liver damage - Dibromochloropropane
- Occupational liver damage - Dimethyl sulfate
- Occupational liver damage - Dimethylnitrosamine
- Occupational liver damage - Dinitrobenzene
- Occupational liver damage - Dinitrophenol
- Occupational liver damage - Dinitrotoluene
- Occupational liver damage - Diphenyl
- Occupational liver damage - Ethanolamines
- Occupational liver damage - Ethyl Acetate
- Occupational liver damage - Ethyl alcohol
- Occupational liver damage - Ethyl Ether
- Occupational liver damage - Ethyl Salicylate
- Occupational liver damage - Ethylene chlorohydrin
- Occupational liver damage - Ethylene Dibromide
- Occupational liver damage - Ethylene dichloride
- Occupational liver damage - Ethylene oxide
- Occupational liver damage - Ethylenediamine
- Occupational liver damage - Germanium
- Occupational liver damage - Hydrazine and derivatives
- Occupational liver damage - Hydrogen bromides
- Occupational liver damage - Hydrogen Cyanide
- Occupational liver damage - Ionizing radiation
- Occupational liver damage - Iron
- Occupational liver damage - Isopropyl acetate
- Occupational liver damage - Kepone pesticides
- Occupational liver damage - Mercaptans
- Occupational liver damage - Methyl acetate
- Occupational liver damage - Methyl Bromide
- Occupational liver damage - Methyl Chloride
- Occupational liver damage - Methylene chloride
- Occupational liver damage - Methylene dianiline
- Occupational liver damage - N,N-Dimethylformamide
- Occupational liver damage - N-butyl acetate
- Occupational liver damage - n-Heptane
- Occupational liver damage - N-N-Dimethylacetamide
- Occupational liver damage - N-Nitrosodimethylamine
- Occupational liver damage - N-propyl acetate
- Occupational liver damage - Naphthalene
- Occupational liver damage - Naphthol
- Occupational liver damage - Nickel
- Occupational liver damage - Nitriles
- Occupational liver damage - Nitrobenzene
- Occupational liver damage - Nitromethane
- Occupational liver damage - Nitroparaffins
- Occupational liver damage - Nitrophenol
- Occupational liver damage - Phenol
- Occupational liver damage - Phosphine
- Occupational liver damage - Phosphorus
- Occupational liver damage - Phthalic Anhydride
- Occupational liver damage - Picric Acid
- Occupational liver damage - Polybrominated biphenyls
- Occupational liver damage - Polychlorinated biphenyls
- Occupational liver damage - Propylene dichloride
- Occupational liver damage - Pyridine
- Occupational liver damage - Pyrogallol
- Occupational liver damage - Selenium
- Occupational liver damage - Stibine
- Occupational liver damage - Styrene/ethyl benzene
- Occupational liver damage - Tetrachloroethane
- Occupational liver damage - Tetrachloroethylene
- Occupational liver damage - Tetramethylthiuram disulfide
- Occupational liver damage - Tetryl
- Occupational liver damage - Thallium
- Occupational liver damage - Thallium sulfate pesticides
- Occupational liver damage - Thorium dioxide
- Occupational liver damage - Tin
- Occupational liver damage - Toluene
- Occupational liver damage - Trichloroethylene
- Occupational liver damage - Trinitrotoluene
- Occupational liver damage - Turpentine
- Occupational liver damage - Uranium
- Occupational liver damage - Vinyl Chloride
- Occupational liver damage - Whole body vibration
- Occupational liver damage - Xylene
- Occupational metal-induced liver damage - Antimony
- Occupational metal-induced liver damage - Arsenic
- Occupational metal-induced liver damage - Barium
- Occupational metal-induced liver damage - Beryllium
- Occupational metal-induced liver damage - Bismuth
- Occupational metal-induced liver damage - Boranes
- Occupational metal-induced liver damage - Boron
- Occupational metal-induced liver damage - Cadmium
- Occupational metal-induced liver damage - Chromium
- Occupational metal-induced liver damage - Cobalt
- Occupational metal-induced liver damage - Copper
- Occupational metal-induced liver damage - Germanium
- Occupational metal-induced liver damage - Gold
- Occupational metal-induced liver damage - Hafnium
- Occupational metal-induced liver damage - Halides
- Occupational metal-induced liver damage - Hydrazines
- Occupational metal-induced liver damage - Iron
- Occupational metal-induced liver damage - Lanthanides
- Occupational metal-induced liver damage - Lead
- Occupational metal-induced liver damage - Manganese
- Occupational metal-induced liver damage - Mercury
- Occupational metal-induced liver damage - Molybdenum
- Occupational metal-induced liver damage - Nickel
- Occupational metal-induced liver damage - Niobium
- Occupational metal-induced liver damage - Phosphorus
- Occupational metal-induced liver damage - Selenium
- Occupational metal-induced liver damage - Tellurium
- Occupational metal-induced liver damage - Thallium
- Occupational metal-induced liver damage - Tin
- Organic acidemia
- Pancreatic Acinar Cell Tumors
- Pancreatic cancer
- Pancreatic cancer, adult
- Pancreatic carcinoma, familial
- Pancreatic Islet Cell Cancer
- Pancreatic islet cell tumors (non-functioning tumor)
- Pancreatoblastoma
- Penicillin-induced Immune Hemolytic Anemia
- Percocet overdose
- Pernicious anemia
- Pernicious Anemia, Juvenile type
- PFIC
- Phenothiazine antenatal infection
- Plant toxin-induced liver damage - Albitocin
- Plant toxin-induced liver damage - Cycasin
- Plant toxin-induced liver damage - Icterogenin
- Plant toxin-induced liver damage - Indospicine
- Plant toxin-induced liver damage - Lanthana
- Plant toxin-induced liver damage - Ngaione
- Plant toxin-induced liver damage - Nutmeg
- Plant toxin-induced liver damage - Pyrrolidizine
- Plant toxin-induced liver damage - Safrole
- Plant toxin-induced liver damage - Tannic Acid
- Postoperative Jaundice
- Primary Autoimmune Hemolytic Anemia
- Primary biliary cirrhosis
- Primary Biliary Cirrhosis 1
- Primary Biliary Cirrhosis 2
- Primary Biliary Cirrhosis 3
- Primary Cold Autoimmune Hemolytic Anemia
- Primary sclerosing cholangitis
- Pseudo-torch syndrome
- Psychotropic agent-induced liver damage
- Psychotropic agent-induced liver damage - Benzodiazepine
- Psychotropic agent-induced liver damage - Butyrophenone
- Psychotropic agent-induced liver damage - monoamine oxidase inhibitors
- Psychotropic agent-induced liver damage - Phenothiazines
- Psychotropic agent-induced liver damage - Thioxanthene
- Psychotropic agent-induced liver damage - tricyclic antidepressant
- Pyruvate Kinase Deficiency
- Pyruvate kinase deficiency, hemolytic anemia
- Pyruvate kinase deficiency, liver type
- Pyruvate kinase deficiency, muscle type
- Quinidine-induced Immune Hemolytic Anemia
- Relapsing fever
- Reticuloendotheliosis
- Rh deficiency syndrome
- Rh Disease
- Rhabdomyosarcoma, embryonal
- Rhabdomyosarcoma, embryonal 1
- Rhabdomyosarcoma, embryonal 2
- Sarcoma botryoides
- Secondary Autoimmune Hemolytic Anemia
- Secondary Biliary Cirrhosis
- Secondary Cold Autoimmune Hemolytic Anemia
- Sepsis
- Septo-Optic Dysplasia
- Sickle Cell Anemia
- Sickle cell crisis
- Soto's Syndrome
- Spherocytic anemia
- Spherocytosis, type 1
- Spherocytosis, type 2
- Spherocytosis, type 3
- Spherocytosis, type 4
- Spherocytosis, type 5
- Spleen Cancer
- Spleen neoplasm
- Sulfone syndrome
- Sulphonamide -induced Immune Hemolytic Anemia
- Summerskill-Walshe-Tygstrup syndrome
- Thalassemia
- Thrombotic thrombocytopenic purpura, acquired
- Thrombotic thrombocytopenic purpura, congenital
- Thyroid agenesis
- TORCH Syndrome
- Toxic mushrooms - Monomethylhydrazine
- Transfusion Reaction
- Trichomegaly cataract hereditary spherocytosis
- Triosephosphate isomerase 1
- UDP-Galactose-4-epimerase deficiency
- Viral Hepatitis
- Viral meningitis
- Visceral steatosis
- Vitamin B12 Deficiency
- Vitamin C Overdose
- Warm Autoimmune Hemolytic Anemia
- Warm-reacting-antibody haemolytic anemia
- Warm-reacting-antibody hemolytic anemia
- Weil syndrome
- Weil's syndrome
- Wilson's Disease
- Wolman disease
- Wyatt disease
- X-linked alpha thalassemia mental retardation syndrome (ATR-X)
- X-linked lymphoproliferative syndrome
- X-linked sideroblastic anemia
- Xanthogranulomatous cholecystitis
- Xerocytosis, heriditary
- Yellow fever
- Zellweger Syndrome
- Zieve syndrome
Medications or substances causing Jaundice:
The following drugs, medications, substances or toxins are some of the possible
causes of Jaundice as a symptom.
This list is incomplete and various other drugs or substances
may cause your symptoms.
Always advise your doctor of any medications or treatments you are using,
including prescription, over-the-counter, supplements, herbal or alternative treatments.
See full list of 401
medications causing Jaundice
Drug interactions causing Jaundice:
When combined, certain drugs, medications, substances or toxins may react
causing Jaundice as a symptom.
The list below is incomplete and various other drugs or substances may cause your symptoms.
Always advise your doctor of any medications or treatments you are using,
including prescription, over-the-counter, supplements, herbal or alternative treatments.
- Fusidic Acid and Ritonavir, Saquinavir interaction
- Rifampin and Pyrazinamide interaction
- Troleandomycin and Oral Contraceptive Agents interaction
- Oral Contraceptive and TAO interaction
- Birth Control Pill and TAO interaction
- more interactions...»
See full list of 105
drug interactions causing Jaundice
What causes Jaundice?
Causes: Jaundice:
Bile materials (bilirubin) in the blood, often from liver diseases such as hepatitis.
Related information on causes of Jaundice:
As with all medical conditions,
there may be many causal factors.
Further relevant information on causes of Jaundice may be found in:
Causes of Jaundice: Online Medical Books
16 MEDICAL BOOKS ONLINE!
Review excerpts from medical books online, free, without registration,
for more information about the causes of Jaundice.
Jaundice:
Differential Diagnosis
(In a Page: Signs and Symptoms)
-
Viral hepatitis
–Fatigue, anorexia, fever, nausea, vomiting, dark urine, light-colored (acholic) loose stools, RUQ pain, hepatomegaly, and/or pruritis
-
Alcoholic hepatitis
–Associated with fever, leukocytosis, and AST:ALT ratio >2
-
Nonalcoholic steatohepatitis or nonalchoholic fatty liver disease
–Associated with obesity, diabetes,
hyperlipidemia and medications
-
Cholecystitis
–RUQ pain, fever, leukocytosis
–Female, fertile, fat, forty
–Murphy's sign: Pain upon palpation of the
gallbladder while taking a deep breath
-
Drugs and toxins
–Acetaminophen, alcohol, estrogens, isoniazid, chlorpromazine, erythromycin, nitrofurantoin, rifampin
-
Gilbert's syndrome
–Decreased conjugation of bilirubin, especially with dehydration, fasting, infection
Sepsis
Malignancy (liver, pancreas, gallbladder/common bile duct, metastatic)
-
Liver infiltration
–Amyloidosis, lymphoma, sarcoidosis, tuberculosis
Total parenteral nutrition (usually requires at least 2 weeks of therapy)
Intravascular hemolysis
-
Cholangitis
–Charcot's triad of fever, RUQ pain, and jaundice
Sickle cell disease
–Chronic hemolysis, hepatic dysfunction
-
Autoimmune hepatitis
–May mimic viral hepatitis
–Females >> males, often 10–30 years old
–Associated with autoimmune disease
(e.g., RA, UC, Sjögren's syndrome, thyroiditis)
Intrahepatic cholestasis of pregnancy
–Pruritus in third trimester
–Resolves after delivery
Hereditary cholestatic disorders (e.g., Dubin-Johnson syndrome, Rotor syndrome)
Physiologic jaundice of newborn
» READ BOOK EXCERPT ONLINE »
Source: In a Page: Signs and Symptoms, 2004
Jaundice in Infants – Direct:
Differential Diagnosis
(In A Page: Pediatric Signs and Symptoms)
- Bile duct obstruction
–Biliary atresia: Represents the most frequent cause for liver transplantation in the pediatric patient; prompt diagnosis is crucial, as patient outcome is better if intervention comes before 60 days of life
–Choledochal cyst
–Common bile duct gallstone
–Choledochocele
–Bile duct stricture
–Alagille syndrome
–Caroli disease
–Congenital hepatic fibrosis
- Neonatal hepatitis
–Idiopathic hepatitis: Diagnosis of exclusion that should be made only when other causes are excluded; accounts for 60% of patients with neonatal cholestasis
–Infections: TORCH, hepatitis B, HIV, E. coli, adenovirus, enterovirus, parvovirus B16, tuberculosis, listeriosis, malaria
-
Metabolic disorders
–α-1 antitrypsin deficiency
–Cystic fibrosis
–Hypothyroidism
–Neonatal iron storage disease
–Amino acids: tyrosinemia
–Carbohydrates: Galactosemia, fructosemia
–Lipids: Niemann-Pick, Gaucher, Wolman,
cholesterol ester storage disease
–Mitochondropathies
–Bile acid synthetic disorders
–Peroxisomal: Zellweger syndrome
–Urea cycle defects
-
Toxins
–Total parenteral nutrition
–Drugs: Trimethaprim-sulfamethoxazole,
anticonvulsants
-
Miscellaneous
–Sepsis/hypoperfusion
–Erythrophagocytic lymphohistiocytosis
–Extracorporeal membrane oxygenation
–Trisomy 17, 18, 21
–Neonatal lupus erythematosus
–Donohue syndrome
–Rotor syndrome
–Dubin-Johnson syndrome
–Byler disease (PFIC type 1)
–Cholestasis of North-American Indians
–Nielsen syndrome
» READ BOOK EXCERPT ONLINE »
Source: In A Page: Pediatric Signs and Symptoms, 2007
Jaundice in Infants – Indirect:
Differential Diagnosis
(In A Page: Pediatric Signs and Symptoms)
-
Icterus neonatorum (physiologic jaundice)
–The most common form of indirect jaundice in infants under 14 days of age
–Caused by increased bilirubin production with transient limited conjugation abilities
-
Breast-feeding jaundice
–Occurs in first week of life in 13% of breast-fed infants
–Secondary to poor volume intake
-
Breast-milk jaundice
–Occurs in about 2% of breast-fed infants after day 7 of life
–Secondary to glucuronidase in breast milk
-
Hematologic: Hemolysis increases bili load
–Rh incompatability
–ABO incompatability
–Glucose-6-phosphate dehydrogenase (G6PD)
deficiency
–Pyruvate kinase deficiency
–Hereditary spherocytosis
–Elliptocytosis
–Thalassemia
–Polycythemia
-
Extravascular blood
–Cephalohematoma
–Trauma
–Swallowed maternal blood
-
Endocrinologic
–Hypothyroidism
–Maternal diabetes
-
Sepsis
-
Metabolic
–Crigler-Najjar I
–Crigler-Najjar II (Arias syndrome)
–Crigler-Najjar III
-
Cardiopulmonary
–Congestive heart failure
–Patent ductus arteriosus
–Portal vein thrombosis
-
Anatomic
–Pyloric stenosis
–Duodenal atresia/stenosis
–Duodenal web
-
Drugs
–Oxytocin
–Sulfonamides
–Ceftriaxone
–Chuen-Lin
-
Lucey-Driscoll syndrome
» READ BOOK EXCERPT ONLINE »
Source: In A Page: Pediatric Signs and Symptoms, 2007
Jaundice:
Medical causes
(Handbook of Signs & Symptoms (Third Edition))
Carcinoma
Cancer of the ampulla of Vater initially produces fluctuating jaundice, mild abdominal pain, a recurrent fever, and chills
Occult bleeding may be its first sign. Other findings include weight loss, pruritus, and back pain.
Hepatic cancer (primary liver cancer or another cancer that has metastasized to the liver) may cause jaundice by causing obstruction of the bile duct. Even advanced cancer causes nonspecific signs and symptoms, such as right upper quadrant discomfort and tenderness, nausea, weight loss, and a slight fever. Examination may reveal irregular, nodular, firm hepatomegaly; ascites; peripheral edema; a bruit heard over the liver; and a right upper quadrant mass.
Withpancreatic cancer,progressive jaundice — possibly with pruritus — may be the only sign. Related early findings are nonspecific, such as weight loss and back or abdominal pain. Other signs and symptoms include anorexia, nausea and vomiting, a fever, steatorrhea, fatigue, weakness, diarrhea, pruritus, and skin lesions (usually on the legs).
Cholangitis
Obstruction and infection in the common bile duct cause Charcot’s triad: jaundice, right upper quadrant pain, and a high fever with chills.
Cholecystitis
Cholecystitis produces nonobstructive jaundice in about 25% of patients
Biliary colic typically peaks abruptly, persisting for 2 to 4 hours. The pain then localizes to the right upper quadrant and becomes constant. Local inflammation or passage of stones to the common bile duct causes jaundice. Other findings include nausea, vomiting (usually indicating the presence of a stone), a fever, profuse diaphoresis, chills, tenderness on palpation, a positive Murphy’s sign and, possibly, abdominal distention and rigidity.
Cholelithiasis
Cholelithiasis commonly causes jaundice and biliary colic
It’s characterized by severe, steady pain in the right upper quadrant or epigastrium that radiates to the right scapula or shoulder and intensifies over several hours. Accompanying signs and symptoms include nausea and vomiting, tachycardia, and restlessness. Occlusion of the common bile duct causes a fever, chills, jaundice, clay-colored stools, and abdominal tenderness. After consuming a fatty meal, the patient may experience vague epigastric fullness and dyspepsia.
Cirrhosis
With Laënnec’s cirrhosis, mild to moderate jaundice with pruritus usually signals hepatocellular necrosis or progressive hepatic insufficiency
Common early findings include ascites, weakness, leg edema, nausea and vomiting, diarrhea or constipation, anorexia, weight loss, and right upper quadrant pain. Massive hematemesis and other bleeding tendencies may also occur. Other findings include an enlarged liver and parotid gland, clubbed fingers, Dupuytren’s contracture, mental changes, asterixis, fetor hepaticus, spider angiomas, and palmar erythema. Males may exhibit gynecomastia, scanty chest and axillary hair, and testicular atrophy; females may experience menstrual irregularities.
With primary biliary cirrhosis,fluctuating jaundice may appear years after the onset of other signs and symptoms, such as pruritus that worsens at bedtime (commonly the first sign), weakness, fatigue, weight loss, and vague abdominal pain. Itching may lead to skin excoriation. Associated findings include hyperpigmentation; indications of malabsorption, such as nocturnal diarrhea, steatorrhea, purpura, and osteomalacia; hematemesis from esophageal varices; ascites; edema; xanthelasmas; xanthomas on the palms, soles, and elbows; and hepatomegaly.
Dubin-Johnson syndrome
With Dubin-Johnson syndrome, which is a rare, chronic inherited syndrome, fluctuating jaundice that increases with stress is the major sign, appearing as late as age 40
Related findings include slight hepatic enlargement and tenderness, upper abdominal pain, nausea, and vomiting.
Heart failure
Jaundice due to liver dysfunction occurs in patients with severe right-sided heart failure
Other effects include jugular vein distention, cyanosis, dependent edema of the legs and sacrum, steady weight gain, confusion, hepatomegaly, nausea and vomiting, abdominal discomfort, and anorexia due to visceral edema. Ascites are a late sign. Oliguria, marked weakness, and anxiety may also occur. If left-sided heart failure develops first, other findings may include fatigue, dyspnea, orthopnea, paroxysmal nocturnal dyspnea, tachypnea, arrhythmias, and tachycardia.
Hepatic abscess
Multiple abscesses may cause jaundice, but the primary effects are a persistent fever with chills and sweating
Other findings include steady, severe pain in the right upper quadrant or midepigastrium that may be referred to the shoulder; nausea and vomiting; anorexia; hepatomegaly; an elevated right hemidiaphragm; and ascites.
Hepatitis
Dark urine and clay-colored stools usually develop before jaundice in the late stages of acute viral hepatitis
Early systemic signs and symptoms vary and include fatigue, nausea, vomiting, malaise, arthralgia, myalgia, a headache, anorexia, photophobia, pharyngitis, a cough, diarrhea or constipation, and a low-grade fever associated with liver and lymph node enlargement. During the icteric phase (which subsides within 2 to 3 weeks unless complications occur), systemic signs subside, but an enlarged, palpable liver may be present along with weight loss, anorexia, and right upper quadrant pain and tenderness.
Pancreatitis (acute)
Edema of the head of the pancreas and obstruction of the common bile duct can cause jaundice; however, the primary symptom of acute pancreatitis is usually severe epigastric pain that commonly radiates to the back
Lying with the knees flexed on the chest or sitting up and leaning forward brings relief. Early associated signs and symptoms include nausea, persistent vomiting, abdominal distention, and Turner’s or Cullen’s sign. Other findings include a fever, tachycardia, abdominal rigidity and tenderness, hypoactive bowel sounds, and crackles.
Severe pancreatitis produces extreme restlessness; mottled skin; cold, diaphoretic extremities; paresthesia; and tetany — the last two being symptoms of hypocalcemia. Fulminant pancreatitis causes massive hemorrhage.
Sickle cell anemia
Hemolysis produces jaundice in the patient with sickle cell anemia
Other findings include impaired growth and development, increased susceptibility to infection, life-threatening thrombotic complications and, commonly, leg ulcers, swollen (painful) joints, a fever, and chills. Bone aches and chest pain may also occur. Severe hemolysis may cause hematuria and pallor, chronic fatigue, weakness, dyspnea (or dyspnea on exertion), and tachycardia. The patient may also have splenomegaly. During a sickle cell crisis, the patient may have severe bone, abdominal, thoracic, and muscular pain; a low-grade fever; and increased weakness, jaundice, and dyspnea.
Other causes
Drugs
Many drugs may cause hepatic injury and resultant jaundice
Examples include acetaminophen, phenylbutazone, I.V. tetracycline, isoniazid, hormonal contraceptives, sulfonamides, mercaptopurine, erythromycin estolate, niacin, troleandomycin, androgenic steroids, 3-hydroxy-3-methylglutaryl reductase inhibitors, phenothiazines, ethanol, methyldopa, rifampin, and dilantin.
Treatments
Upper abdominal surgery may cause postoperative jaundice, which occurs secondary to hepatocellular damage from the manipulation of organs, leading to edema and obstructed bile flow; from the administration of halothane; or from prolonged surgery resulting in shock, blood loss, or blood transfusion.
A surgical shunt used to reduce portal hypertension (such as a portacaval shunt) may also produce jaundice.
» READ BOOK EXCERPT ONLINE »
Source: Handbook of Signs & Symptoms (Third Edition), 2006
Jaundice [Icterus]:
Medical causes
(Professional Guide to Signs & Symptoms (Fifth Edition))
Agnogenic myeloid metaplasia
This myeloproliferative disorder of the bone marrow may cause jaundice. Its typical effects, however, are associated with anemia, including fatigue, weakness, anorexia, massive splenomegaly, hepatomegaly, purpura, and bleeding tendencies.
Carcinoma
Cancer of the ampulla of Vater initially produces fluctuating jaundice, mild abdominal pain, recurrent fever, and chills. Occult bleeding may be its first sign. Other findings include weight loss, pruritus, and back pain.
Hepatic cancer (primary liver cancer or another cancer that has metastasized to the liver) may cause jaundice by causing obstruction of the bile duct. Even advanced cancer causes nonspecific signs and symptoms, such as right-upper-quadrant discomfort and tenderness, nausea, weight loss, and slight fever. Examination may reveal irregular, nodular, firm hepatomegaly, ascites, peripheral edema, a bruit heard over the liver, and a right-upper-quadrant mass.
With pancreatic cancer, progressive jaundice—possibly with pruritus—may be the only sign. Related early findings are nonspecific, such as weight loss and back or abdominal pain. Other signs and symptoms include anorexia, nausea and vomiting, fever, steatorrhea, fatigue, weakness, diarrhea, pruritus, and skin lesions (usually on the legs).
Cholangitis
Obstruction and infection in the common bile duct cause Charcot’s triad: jaundice, right-upper-quadrant pain, and high fever with chills.
Cholecystitis
This disorder produces nonobstructive jaundice in about 25% of patients. Biliary colic typically peaks abruptly, persisting for 2 to 4 hours. The pain then localizes to the right upper quadrant and becomes constant. Local inflammation or passage of stones to the common bile duct causes jaundice. Other findings include nausea, vomiting (usually indicating the presence of a stone), fever, profuse diaphoresis, chills, tenderness on palpation, a positive Murphy’s sign, and, possibly, abdominal distention and rigidity.
Cholelithiasis
This disorder commonly causes jaundice and biliary colic. It’s characterized by severe, steady pain in the right upper quadrant or epigastrium that radiates to the right scapula or shoulder and intensifies over several hours. Accompanying signs and symptoms include nausea and vomiting, tachycardia, and restlessness. Occlusion of the common bile duct causes fever, chills, jaundice, clay-colored stools, and abdominal tenderness. After consuming a fatty meal, the patient may experience vague epigastric fullness and dyspepsia.
Cholestasis
With benign, recurrent intrahepatic cholestasis, the patient experiences prolonged attacks of jaundice (sometimes spaced several years apart) accompanied by pruritus. Other signs and symptoms are similar to those of hepatitis—fatigue, nausea, weight loss, anorexia, pale stools, and right-upper-quadrant pain.
Cirrhosis
With Laënnec’s cirrhosis, mild to moderate jaundice with pruritus usually signals hepatocellular necrosis or progressive hepatic insufficiency. Common early findings include ascites, weakness, leg edema, nausea and vomiting, diarrhea or constipation, anorexia, weight loss, and right-upper-quadrant pain. Massive hematemesis and other bleeding tendencies may also occur. Other findings include an enlarged liver and parotid gland, clubbed fingers, Dupuytren’s contracture, mental changes, asterixis, fetor hepaticus, spider angiomas, and palmar erythema. Males may exhibit gynecomastia, scanty chest and axillary hair, and testicular atrophy; females may experience menstrual irregularities.
With primary biliary cirrhosis, fluctuating jaundice may appear years after the onset of other signs and symptoms, such as pruritus that worsens at bedtime (commonly the first sign), weakness, fatigue, weight loss, and vague abdominal pain. Itching may lead to skin excoriation. Associated findings include hyperpigmentation; indications of malabsorption, such as nocturnal diarrhea, steatorrhea, purpura, and osteomalacia; hematemesis from esophageal varices; ascites; edema; xanthelasmas; xanthomas on the palms, soles, and elbows; and hepatomegaly.
Dubin-Johnson syndrome
With this rare, chronic inherited syndrome, fluctuating jaundice that increases with stress is the major sign, appearing as late as age 40. Related findings include slight hepatic enlargement and tenderness, upper abdominal pain, nausea, and vomiting.
Glucose-6-phosphate dehydrogenase deficiency
Acute intravascular hemolysis following ingestion of such drugs as quinine or aspirin causes jaundice, pallor, dyspnea, tachycardia, and malaise. Palpation may reveal splenomegaly and hepatomegaly.
Heart failure
Jaundice due to liver dysfunction occurs in patients with severe right-sided heart failure. Other effects include jugular vein distention, cyanosis, dependent edema of the legs and sacrum, steady weight gain, confusion, hepatomegaly, nausea and vomiting, abdominal discomfort, and anorexia due to visceral edema. Ascites is a late sign. Oliguria, marked weakness, and anxiety may also occur. If left-sided heart failure develops first, other findings may include fatigue, dyspnea, orthopnea, paroxysmal nocturnal dyspnea, tachypnea, arrhythmias, and tachycardia.
Hemolytic anemia (acquired)
This disorder may produce prominent jaundice along with dyspnea, fatigue, pallor, tachycardia, and palpitations. Rapid hemolysis causes chills, fever, irritability, headache, and abdominal pain; severe hemolysis causes signs of shock.
Hepatic abscess
Multiple abscesses may cause jaundice, but the primary effects are persistent fever with chills and sweating. Other findings include steady, severe pain in the right upper quadrant or midepigastrium that may be referred to the shoulder; nausea and vomiting; anorexia; hepatomegaly; elevated right hemidiaphragm; and ascites.
Hepatitis
Dark urine and clay-colored stools usually develop before jaundice in the late stages of acute viral hepatitis. Early systemic signs and symptoms vary and include fatigue, nausea, vomiting, malaise, arthralgias, myalgias, headache, anorexia, photophobia, pharyngitis, cough, diarrhea or constipation, and a low-grade fever associated with liver and lymph node enlargement. During the icteric phase (which subsides within 2 to 3 weeks unless complications occur), systemic signs subside, but an enlarged, palpable liver may be present along with weight loss, anorexia, and right-upper-quadrant pain and tenderness.
Leptospirosis
Severe leptospirosis (Weil’s disease) may cause jaundice. This disorder begins suddenly with a frontal headache, severe muscle aches in the thighs and lumbar area, cutaneous hyperesthesia, abdominal pain, nausea, conjunctival suffusion, and vomiting. Chills and a rapidly rising fever follow. Signs and symptoms of meningeal irritation include drowsiness, decreased mentation, stiff neck, and positive Kernig’s and Brudzinski’s signs. Right-upper-quadrant tenderness, hepatomegaly, and jaundice indicate hepatic involvement; proteinuria, pyuria, and hematuria indicate renal involvement. Epistaxis, hematemesis, melena, and hemoptysis may also occur.
Pancreatitis (acute)
Edema of the head of the pancreas and obstruction of the common bile duct can cause jaundice; however, this disorder’s primary symptom is usually severe epigastric pain that commonly radiates to the back. Lying with the knees flexed on the chest or sitting up and leaning forward brings relief. Early associated signs and symptoms include nausea, persistent vomiting, abdominal distention, and Turner’s or Cullen’s sign. Other findings include fever, tachycardia, abdominal rigidity and tenderness, hypoactive bowel sounds, and crackles.
Severe pancreatitis produces extreme restlessness; mottled skin; cold, diaphoretic extremities; paresthesia; and tetany—the last two being symptoms of hypocalcemia. Fulminant pancreatitis causes massive hemorrhage.
Sickle cell anemia
Hemolysis produces jaundice in patients with this disorder. Other findings include impaired growth and development, increased susceptibility to infection, life-threatening thrombotic complications and, commonly, leg ulcers, (painful) swollen joints, fever, and chills. Bone aches and chest pain may also occur. Severe hemolysis may cause hematuria and pallor, chronic fatigue, weakness, dyspnea (or dyspnea on exertion), and tachycardia. The patient may also have splenomegaly. During a sickle cell crisis, the patient may have severe bone, abdominal, thoracic, and muscular pain; low-grade fever; and increased weakness, jaundice, and dyspnea.
Zieve syndrome
Caused by alcohol abuse, this relatively rare disorder produces abdominal pain and a sudden onset of severe jaundice. However, spider angiomas, ascites, and other signs of advanced liver disease are absent.
Other causes
Drugs
Many drugs may cause hepatic injury and resultant jaundice. Examples include acetaminophen, I.V. tetracycline, isoniazid, hormonal contraceptives, sulfonamides, mercaptopurine, erythromycin estolate, niacin, troleandomycin, androgenic steroids, HMG-CoA reductase inhibitors, phenothiazines, ethanol, methyldopa, rifampin, and phenytoin.
Treatments
Upper abdominal surgery may cause postoperative jaundice, which occurs secondary to hepatocellular damage from the manipulation of organs, leading to edema and obstructed bile flow; from the administration of halothane; or from prolonged surgery resulting in shock, blood loss, or blood transfusion.
A surgical shunt used to reduce portal hypertension (such as a portacaval shunt) may also produce jaundice.
» READ BOOK EXCERPT ONLINE »
Source: Professional Guide to Signs & Symptoms (Fifth Edition), 2006
Jaundice:
Differential Overview
(Field Guide to Bedside Diagnosis)
Conjugated
❑ Viral hepatitis
❑ Gallstone obstruction
❑ Drugs
❑ Carotinemia
❑ Alcohol-induced hepatitis
❑ Cirrhosis
❑ Pregnancy (cholestatic)
❑ Postoperative
❑ Metastatic cancer
❑ Pancreatic cancer
❑ Ampullary carcinoma
❑ Hepatoma
❑ Sclerosing cholangitis
❑ Primary biliary cirrhosis
❑ Leptospirosis
❑ Hepatic vein obstruction (Budd-Chiari)
❑ Hemochromatosis
Unconjugated
❑ Hemolysis
❑ Gilbert syndrome
❑ Sepsis
» READ BOOK EXCERPT ONLINE »
Source: Field Guide to Bedside Diagnosis, 2007
Jaundice:
Medical causes
(Signs & Symptoms: A 2-in-1 Reference for Nurses)
Carcinoma
Cancer of the ampulla of Vater initially produces fluctuating jaundice, mild abdominal pain, recurrent fever, and chills. Occult bleeding may be its first sign. Other findings include weight loss, pruritus, and back pain.
Hepatic cancer (primary liver cancer or metastases to the liver) may cause jaundice by causing obstruction of the bile duct. Even advanced cancer causes nonspecific signs and symptoms, such as right-upper-quadrant discomfort and tenderness, nausea, weight loss, and slight fever. Examination may reveal irregular, nodular, firm hepatomegaly, ascites, peripheral edema, a bruit heard over the liver, and a right-upper-quadrant mass.
With pancreatic cancer, progressive jaundice — possibly with pruritus — may be the only sign. Related early findings are nonspecific, such as weight loss and back or abdominal pain. Other signs and symptoms include anorexia, nausea and vomiting, fever, steatorrhea, fatigue, weakness, diarrhea, pruritus, and skin lesions (usually on the legs).
Cholangitis
Obstruction and infection in the common bile duct cause Charcot’s triad: jaundice, right-upper-quadrant pain, and high fever with chills. The patient may also report pruritus. Acholic or hypocholic stools may be present.
Cholecystitis
Cholecystitis produces nonobstructive jaundice in about 25% of patients. Biliary colic typically peaks abruptly, persisting for 2 to 4 hours. The pain then localizes to the right upper quadrant and becomes constant. Local inflammation or passage of stones to the common bile duct causes jaundice. Other findings include nausea, vomiting (usually indicating the presence of a stone), fever, profuse diaphoresis, chills, tenderness on palpation, a positive Murphy’s sign and, possibly, abdominal distention and rigidity.
Cholelithiasis
Cholelithiasis commonly causes jaundice and biliary colic. It’s characterized by severe, steady pain in the right upper quadrant or epigastrium that radiates to the right scapula or shoulder and intensifies over several hours. Accompanying signs and symptoms include nausea and vomiting, tachycardia, and restlessness. Occlusion of the common bile duct causes fever, chills, jaundice, clay-colored stools, and abdominal tenderness. After consuming a fatty meal, the patient may experience vague epigastric fullness and dyspepsia.
Cholestasis
With benign, recurrent intrahepatic cholestasis, the patient experiences prolonged attacks of jaundice (sometimes spaced several years apart) accompanied by pruritus. Other signs and symptoms are similar to those of hepatitis — fatigue, nausea, weight loss, anorexia, pale stools, and right-upper-quadrant pain.
Cirrhosis
With Laënnec’s cirrhosis, mild to moderate jaundice with pruritus usually signals hepatocellular necrosis or progressive hepatic insufficiency. Common early findings include ascites, weakness, leg edema, nausea and vomiting, diarrhea or constipation, anorexia, weight loss, and right-upper-quadrant pain. Massive hematemesis and other bleeding tendencies may also occur. Other findings include an enlarged liver and parotid gland, clubbed fingers, Dupuytren’s contracture, mental changes, asterixis, fetor hepaticus, spider angiomas, and palmar erythema. Males may exhibit gynecomastia, scanty chest and axillary hair, and testicular atrophy; females may experience menstrual irregularities.
With primary biliary cirrhosis, fluctuating jaundice may appear years after the onset of other signs and symptoms, such as pruritus that worsens at bedtime (commonly the first sign), weakness, fatigue, weight loss, and vague abdominal pain. Itching may lead to skin excoriation. Associated findings include hyperpigmentation; indications of malabsorption, such as nocturnal diarrhea, steatorrhea, purpura, and osteomalacia; hematemesis from esophageal varices; ascites; edema; xanthelasmas; xanthomas on the palms, soles, and elbows; and hepatomegaly.
Glucose-6-phosphate dehydrogenase deficiency
Acute intravascular hemolysis following ingestion of such drugs as quinine or aspirin causes jaundice, pallor, dyspnea, tachycardia, and malaise. Palpation may reveal splenomegaly and hepatomegaly.
Heart failure
Jaundice due to liver dysfunction occurs in patients with severe right-sided heart failure. Other effects include jugular vein distention, cyanosis, dependent edema of the legs and sacrum, steady weight gain, confusion, hepatomegaly, nausea and vomiting, abdominal discomfort, and anorexia due to visceral edema. Ascites is a late sign. Oliguria, marked weakness, and anxiety may also occur. If left-sided heart failure develops first, other findings may include fatigue, dyspnea, orthopnea, paroxysmal nocturnal dyspnea, tachypnea, arrhythmias, and tachycardia.
Hemolytic anemia (acquired)
Acquired hemolytic anemia may produce prominent jaundice along with dyspnea, fatigue, pallor, tachycardia, and palpitations. Rapid hemolysis causes chills, fever, irritability, headache, and abdominal pain; severe hemolysis causes signs of shock.
Hepatitis
Dark urine and clay-colored stools usually develop before jaundice in the late stages of acute viral hepatitis. Early systemic signs and symptoms vary and include fatigue, nausea, vomiting, malaise, arthralgias, myalgias, headache, anorexia, photophobia, pharyngitis, cough, diarrhea or constipation, and a low-grade fever associated with liver and lymph node enlargement. During the icteric phase (which subsides within 2 to 3 weeks unless complications occur), systemic signs subside, but an enlarged, palpable liver may be present along with weight loss, anorexia, and right-upper-quadrant pain and tenderness.
Pancreatitis (acute)
Pancreatitis can cause jaundice; however, this disorder’s primary symptom is usually severe epigastric pain that commonly radiates to the back. Lying with the knees flexed on the chest or sitting up and leaning forward brings relief. Early associated signs and symptoms include nausea, persistent vomiting, abdominal distention, and Turner’s or Cullen’s sign. Other findings include fever, tachycardia, abdominal rigidity and tenderness, hypoactive bowel sounds, and crackles.
Severe pancreatitis produces extreme restlessness; mottled skin; cold, diaphoretic extremities; paresthesia; and tetany — the last two being symptoms of hypocalcemia. Fulminant pancreatitis causes massive hemorrhage.
Sickle cell anemia
Hemolysis produces jaundice in patients with sickle cell anemia. Other findings include impaired growth and development, increased susceptibility to infection, life-threatening thrombotic complications and, commonly, leg ulcers, swollen joints (sometimes painful), fever, and chills. Bone aches and chest pain may also occur. Severe hemolysis may cause hematuria and pallor, chronic fatigue, weakness, dyspnea (or dyspnea on exertion), and tachycardia. The patient may also have splenomegaly. During a sickle cell crisis, the patient may have severe bone, abdominal, thoracic, and muscular pain; low-grade fever; and increased weakness, jaundice, and dyspnea.
Other causes
Drugs
Many drugs may cause hepatic injury and resultant jaundice. Examples include acetaminophen, phenylbutazone, I.V. tetracycline, isoniazid, hormonal contraceptives, sulfonamides, mercaptopurine, erythromycin estolate, niacin, troleandomycin, androgenic steroids, HMG-CoA reductase inhibitors, phenothiazines, ethanol, methyldopa, rifampin, and dilantin.
Treatments
Upper abdominal surgery may cause postoperative jaundice, which occurs secondary to hepatocellular damage from the manipulation of organs. Postoperative jaundice may lead to edema and obstructed bile flow from the administration of halothane or from prolonged surgery resulting in shock, blood loss, or blood transfusion. A surgical shunt used to reduce portal hypertension (such as a portacaval shunt) may also produce jaundice.
» READ BOOK EXCERPT ONLINE »
Source: Signs & Symptoms: A 2-in-1 Reference for Nurses, 2007
Jaundice:
Principal Causes of Unconjugated Hyperbilirubinemia
(The Diagnostic Approach to Symptoms and Signs in Pediatrics)
- Neonatalonset
- Increasedbilirubin production
- Physiologic
- Hemolytic anemia
- Isoimmunization
- Red cell enzyme defects
- Glucose-6-phosphatedehydrogenase deficiency
- Pyruvate kinase deficiency
- Other enzyme defects
- Red cell membrane defects
- Hereditaryspherocytosis
- Hereditary elliptocytosis
- Hereditary stomatocytosis
- Infantile pyknocytosis
- Septicemia
- Polycythemia
- Enclosed hematoma
- Decreased bilirubin uptake, storage,or metabolism
- Physiologic
- Hypoxia and acidosis
- Hypoalbuminemia
- Increased serum fatty acids
- Septicemia
- Drugs
- Hypothyroidism
- Lucey-Driscoll syndrome (transientfamilial neonatal hyperbilirubinemia)
- Crigler-Najjar syndrome (types I andII)
- Increased enterohepatic circulation
- Physiologic
- Breast-feeding–related jaundice
- Intestinal obstruction
- Postneonatal onset
- Increasedbilirubin production
- Hemolytic anemia
- Septicemia
- Decreased bilirubin uptake, storage,or metabolism
- Gilbertsyndrome
- Septicemia
» READ BOOK EXCERPT ONLINE »
Source: The Diagnostic Approach to Symptoms and Signs in Pediatrics, 2006
Jaundice [Icterus]:
Medical causes
(Nursing: Interpreting Signs and Symptoms)
Carcinoma.Cancer of the ampulla of Vater initially produces fluctuating jaundice, mild abdominal pain, a recurrent fever, and chills. Occult bleeding may be its first sign. Other findings include weight loss, pruritus, and back pain.
Hepatic cancer (primary liver cancer or another cancer that has metastasized to the liver) may cause jaundice by causing obstruction of the bile duct. Even advanced cancer causes nonspecific signs and symptoms, such as right upper quadrant discomfort and tenderness, nausea, weight loss, and a slight fever. Examination may reveal irregular, nodular, firm hepatomegaly; ascites; peripheral edema; a bruit heard over the liver; and a right upper quadrant mass.
With pancreatic cancer, progressive jaundice—possibly with pruritus—may be the only sign. Related early findings are nonspecific, such as weight loss and back or abdominal pain. Other signs and symptoms include anorexia, nausea and vomiting, a fever, steatorrhea, fatigue, weakness, diarrhea, pruritus, and skin lesions (usually on the legs).
Cholangitis.Obstruction and infection in the common bile duct cause Charcot's triad: jaundice, right upper quadrant pain, and a high fever with chills.
Cholecystitis.Cholecystitis produces nonobstructive jaundice in about 25% of patients. Biliary colic typically peaks abruptly, persisting for 2 to 4 hours. The pain then localizes to the right upper quadrant and becomes constant. Local inflammation or passage of stones to the common bile duct causes jaundice. Other findings include nausea, vomiting (usually indicating the presence of a stone), a fever, profuse diaphoresis, chills, tenderness on palpation, a positive Murphy's sign and, possibly, abdominal distention and rigidity.
Cholelithiasis.Cholelithiasis commonly causes jaundice and biliary colic. It's characterized by severe, steady pain in the right upper quadrant or epigastrium that radiates to the right scapula or shoulder and intensifies over several hours. Accompanying signs and symptoms include nausea and vomiting, tachycardia, and restlessness. Occlusion of the common bile duct causes a fever, chills, jaundice, clay-colored stools, and abdominal tenderness. After consuming a fatty meal, the patient may experience vague epigastric fullness and dyspepsia.
Cirrhosis.With Laënnec's cirrhosis, mild to moderate jaundice with pruritus usually signals hepatocellular necrosis or progressive hepatic insufficiency. Common early findings include ascites, weakness, leg edema, nausea and vomiting, diarrhea or constipation, anorexia, weight loss, and right upper quadrant pain. Massive hematemesis and other bleeding tendencies may also occur. Other findings include an enlarged liver and parotid gland, clubbed fingers, Dupuytren's contracture, mental changes, asterixis, fetor hepaticus, spider angiomas, and palmar erythema. Males may exhibit gynecomastia, scanty chest and axillary hair, and testicular atrophy; females may experience menstrual irregularities.
With primary biliary cirrhosis, fluctuating jaundice may appear years after the onset of other signs and symptoms, such as pruritus that worsens at bedtime (commonly the first sign), weakness, fatigue, weight loss, and vague abdominal pain. Itching may lead to skin excoriation. Associated findings include hyperpigmentation; indications of malabsorption, such as nocturnal diarrhea, steatorrhea, purpura, and osteomalacia; hematemesis from esophageal varices; ascites; edema; xanthelasmas; xanthomas on the palms, soles, and elbows; and hepatomegaly.
Dubin-Johnson syndrome.With Dubin-Johnson syndrome, which is a rare, chronic inherited syndrome, fluctuating jaundice that increases with stress is the major sign, appearing as late as age 40. Related findings include slight hepatic enlargement and tenderness, upper abdominal pain, nausea, and vomiting.
Heart failure.Jaundice due to liver dysfunction occurs in patients with severe right-sided heart failure. Other effects include jugular vein distention, cyanosis, dependent edema of the legs and sacrum, steady weight gain, confusion, hepatomegaly, nausea and vomiting, abdominal discomfort, and anorexia due to visceral edema. Ascites is a late sign. Oliguria, marked weakness, and anxiety may also occur. If left-sided heart failure develops first, other findings may include fatigue, dyspnea, orthopnea, paroxysmal nocturnal dyspnea, tachypnea, arrhythmias, and tachycardia.
Hepatic abscess.Multiple liver abscesses may cause jaundice, but the primary effects are a persistent fever with chills and sweating. Other findings include steady, severe pain in the right upper quadrant or midepigastrium that may be referred to the shoulder; nausea and vomiting; anorexia; hepatomegaly; an elevated right hemidiaphragm; and ascites.
Hepatitis.Dark urine and clay-colored stools usually develop before jaundice in the late stages of acute viral hepatitis. Early systemic signs and symptoms vary and include fatigue, nausea, vomiting, malaise, arthralgia, myalgia, a headache, anorexia, photophobia, pharyngitis, a cough, diarrhea or constipation, and a low-grade fever associated with liver and lymph node enlargement. During the icteric phase (which subsides within 2 to 3 weeks unless complications occur), systemic signs subside, but an enlarged, palpable liver may be present along with weight loss, anorexia, and right upper quadrant pain and tenderness.
Pancreatitis (acute).Edema of the head of the pancreas and obstruction of the common bile duct can cause jaundice; however, the primary symptom of acute pancreatitis is severe epigastric pain that commonly radiates to the back. Lying with the knees flexed on the chest or sitting up and leaning forward brings relief. Early associated signs and symptoms include nausea, persistent vomiting, abdominal distention, and Turner's or Cullen's sign. Other findings include a fever, tachycardia, abdominal rigidity and tenderness, hypoactive bowel sounds, and crackles.
Severe pancreatitis produces extreme restlessness; mottled skin; cold, dia-phoretic extremities; paresthesia; and tetany—the last two being symptoms of hypocalcemia. Fulminant pancreatitis causes massive hemorrhage.
Sickle cell anemia.Hemolysis produces jaundice in the patient with sickle cell anemia. Other findings include impaired growth and development, increased susceptibility to infection, life-threatening thrombotic complications and, commonly, leg ulcers, swollen (painful) joints, a fever, and chills. Bone aches and chest pain may also occur. Severe hemolysis may cause hematuria and pallor, chronic fatigue, weakness, dyspnea (or dyspnea on exertion), and tachycardia. The patient may also have splenomegaly. During a sickle cell crisis, the patient may have severe bone, abdominal, thoracic, and muscular pain; a low-grade fever; and increased weakness, jaundice, and dyspnea.
Other causes
Drugs.Many drugs may cause hepatic injury and resultant jaundice. Examples include acetaminophen, phenylbutazone, I.V. tetracycline, isoniazid, hormonal contraceptives, sulfonamides, mercaptopurine, erythromycin estolate, niacin, troleandomycin, androgenic steroids, 3-hydroxy-3-methylglutaryl coenzyme A reductase inhibitors, phenothiazines, ethanol, methyldopa, rifampin, and dilantin.
Treatments.Upper abdominal surgery may cause postoperative jaundice, which occurs secondary to hepatocellular damage from the manipulation of organs, leading to edema and obstructed bile flow; from the administration of halothane; or from prolonged surgery resulting in shock, blood loss, or blood transfusion.
A surgical shunt used to reduce portal hypertension (such as a portacaval shunt) may also produce jaundice.
» READ BOOK EXCERPT ONLINE »
Source: Nursing: Interpreting Signs and Symptoms, 2007
Jaundice - Case 15-3: 2-Month-Old Boy:
I. Differential Diagnosis
(Pediatric Complaints and Diagnostic Dilemmas)
The susceptibility of neonates to unconjugated hyperbilirubinemia is favored by
a number of factors, including relative increases in bilirubin production and
enterohepatic circulation along with relative decreases in hepatic uptake and
conjugation. Unconjugated hyperbilirubinemia is a very common occurrence in the
newly born and is usually self-limited and benign. However, if the serum
concentration of bilirubin exceeds 17 mg/dL, the jaundice can no longer be
regarded as physiologic.
Given this predisposition of newborns to an imbalance between bilirubin
generation and hepatic excretory capacity, pathologic or prolonged neonatal
hyperbilirubinemia is often attributable to conditions that exacerbate the
imbalance. For instance, hemolytic diseases (e.g., ABO incompatibility),
polycythemia, and extravascular blood collections (e.g., cephalohematoma,
subgaleal blood, ecchymoses) are conditions that favor increased bilirubin
production. Decreased bilirubin clearance can result from inherited bilirubin
metabolism disorders (e.g., Crigler-Najjar syndrome, Gilbert disease),
hypothyroidism, and circumstances that increase enterohepatic reuptake (e.g.,
breast-feeding, delayed meconium passage). As for older children, Gilbert
syndrome (a genetic disorder of the uridine diphosphoglucuronate
glucuronosyltransferase enzyme system that occurs in about 6% of adults) and
hemolytic anemias are the most common causes of unconjugated bilirubinemia.
» READ BOOK EXCERPT ONLINE »
Source: Pediatric Complaints and Diagnostic Dilemmas, 2003
Jaundice - Case 15-4: 6-Week-Old Girl:
I. Differential Diagnosis
(Pediatric Complaints and Diagnostic Dilemmas)
The differential diagnosis for cholestatic jaundice in the infant is quite
broad, and many excellent and detailed reviews exist. General categories of
disease entities to be considered include
infections, such as hepatitis viruses, TORCH infections, and serious bacterial infections; idiopathic neonatal hepatitis; a long list of metabolic and endocrine diseases, including galactosemia, α1-antitrypsin deficiency, cystic fibrosis, hypothyroidism, hypopituitarism, and
bile acid synthesis defects;
genetic cholestatic syndromes, such as Byler disease; obstructions to bile flow, including biliary atresia, Alagille syndrome, choledochal cysts, and
cholelithiasis; and
iatrogenic causes, such as drug-induced cholestasis or cholestasis related to total parenteral
nutrition.
» READ BOOK EXCERPT ONLINE »
Source: Pediatric Complaints and Diagnostic Dilemmas, 2003
Jaundice - Case 15-6: 5-Week-Old Girl:
I. Differential Diagnosis
(Pediatric Complaints and Diagnostic Dilemmas)
This infant presented with the following signs: a nonobstructive conjugated
hyperbilirubinemia; renal insufficiency with a mild, non
–anion gap metabolic acidosis; poor weight gain; and a heart murmur. Her liver
biopsy revealed cholestasis and bile duct paucity.
Interlobular bile duct paucity is the characteristic, but not unvarying,
pathologic finding in Alagille syndrome; biopsies performed early in the
disease
's course might simply reveal findings of cholestasis, inflammation, or even
ductal proliferation. In addition, bile duct paucity is sometimes seen in
diseases other than Alagille syndrome. So-called nonsyndromic bile duct paucity
can be a feature of congenital infections (e.g., CMV, rubella, syphilis),
metabolic disorders (e.g.,
α 1-antitrypsin deficiency, defects of bile acid synthesis), sclerosing
cholangitis, and idiopathic cholestasis.
» READ BOOK EXCERPT ONLINE »
Source: Pediatric Complaints and Diagnostic Dilemmas, 2003
Jaundice:
Jaundice - etiology
(The 5-Minute Pediatric Consult)
The most common causes of pathologic jaundice:
- Newborn period: Biliary atresia, idiopathic neonatal hepatitis, α1-antitrypsin deficiency, infection
- Older child: Autoimmune hepatitis, viral hepatitis, Wilson disease, biliary obstruction
» READ BOOK EXCERPT ONLINE »
Source: The 5-Minute Pediatric Consult, 2008
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