Dr. Huntley's
Diagnosis
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See what questions
a doctor would ask.
A facial palsy is usually considered to be Bell palsy and it frequently is. Nevertheless, the clinician who begins treatment without ruling out other possibilities will eventually get burned. Anatomy is the key to recalling these possibilities before the patient leaves the office. Follow the facial nerve from its origin along its pathway to its termination and all the causes should come to mind.

FACIAL PARALYSIS
Diseases of the brain and brainstem are considered here. They are usually distinguished from Bell palsy by the presence of other neurologic findings. The mnemonic ANITA will help recall them in an organized fashion.
The facial nerve has a long pathway and along that path it can be destroyed by the following:
The site of termination of the facial nerve should suggest myasthenia gravis, muscular dystrophy, and facial hemiatrophy. These rarely present with an isolated facial palsy.
The clinical picture will frequently help determine the cause of facial paralysis. Peripheral facial palsy as occurs in Bell palsy involves the forehead muscles and there is difficulty in closing the eyelid, whereas central facial palsy involves the face and lips and there is often associated hemiplegia or monoplegia. When there is exclusively a peripheral facial palsy without hearing loss or other neurologic signs, Bell palsy should be strongly suspected, although diabetes and myasthenia gravis need to be excluded. A bilateral peripheral nerve palsy should make one consider Guillain–Barré syndrome and be on the look out for paralysis of the extremities as well. Bilateral facial palsy is also seen in myotonic dystrophy and myasthenia gravis. A “Bell palsy” with hearing loss and an aural discharge should prompt consideration of mastoiditis and petrositis. If there is hearing loss without a discharge, the possibility of an acoustic neuroma or cholesteatoma must be entertained. The association of a central facial palsy with hemiplegia brings up a host of possibilities including subdural hematoma, brain abscess, brain tumor, and cerebrovascular accident. The workup of these conditions is considered on page 545.
If the patient has clinical Bell palsy, one could start a therapy without a workup, but it is wise to get an x-ray of the skull and mastoids to rule out mastoiditis and petrositis and a glucose tolerance test to rule out diabetes. An acetylcholine receptor antibody titer or Tensilon test would only be ordered if the palsy were intermittent or there was other cranial nerve signs. If a middle ear infection or acoustic neuroma is suspected, the patient needs x-ray of the mastoids and petrous bones and a CT scan or MRI of the brain and auditory canal.
Read excerpts from these other book chapters related to Muscle weakness:
Copyright Details: Differential Diagnosis in Primary Care, Copyright © 2008 Williams & Wilkins.
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More About This Book:
Title: Differential Diagnosis in Primary Care Authors: R. Douglas Collins Publisher: Lippincott Williams & Wilkins Copyright: 2007 ISBN: 0-7817-6812-8
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