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| Acute Idiopathic Facial Palsy (Bell's Palsy) |
| Overview |
 | Acute peripheral paralysis of the face produced by a viral
immune-mediated disease. |
 | Possible pathogenesis:
 | After a primary infection, herpes simplex virus became latent in the
cranial and spinal sensory ganglia. |
 | Reactivation of the virus leads to replication of virus within the
ganglion cells. |
 | Virus travels up and down the axons, induces an inflammatory response. |
 | Results in segmental demyelination presented as nerve
paralysis. |
|
 | Incidence: between 15 - 40 / 100,000 population
per year |
 | No evidence of racial predilection |
 | Incidence of Bell's palsy increases with age. |
 | Sexual predilection:
 | Age 10 - 19 years, twice as common in women |
 | Age 40, 1.5 times more common in men. |
 | Pregnant women have 3.3 times more risk than nonpregnant women in the
same age group. |
|
 | Diabetic patients: 4.5 times more likely to develop Bell's palsy. |
 | In 10% of the patients, a positive family history of Bell's palsy is
present. |
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| Clinical features |
 | Sudden onset |
 | Full extent of the paralysis is usually reached in 1 to 14 days. |
 | Early phase: retroauricular pain, facial numbness, epiphora, parageusia,
decreased tearing, and hyperacusis. |
 | Physical findings:
 | Peripheral Facial paresis |
 | Hypoesthesia or dysesthesia of cranial nerves V and IX |
 | Motor paresis of cranial nerves IX and X |
 | Papillitis of the tongue. |
|
 | When severe retroauricular pain is present, Ramsay Hunt syndrome has to
be considered. |
|
| Differential diagnosis of VII weakness |
 | Bells' palsy, usually unilateral, 10% bilateral |
 | Differential of Unilateral Facial weakness
 | Sarcoid |
 | Lyme's disease |
 | Neoplasm or mass |
 | Otitis media |
 | Trauma: skull fracture, facial injury |
|
 | Differential for bilateral VII palsy
 | Melkersson-Rosenthal syndrome
 | Recurrent facial palsy with facial edema, Unilateral or bilateral |
 | Lingua plicata (Scrotal tongue) |
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 | Möbius syndrome: Facial paresis with ophthalmoplegia |
 | Guillain-Barré Syndrome |
 | Myasthenia gravis |
 | Motor neuron disease |
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| Prognosis |
 | Complete recovery in 60 to 80% |
 | Prognostic factors:
 | Age: younger patient has better prognosis. |
 | Incomplete paralysis tends to recover completely. |
 | If recovery begins between days 10 and 21, a satisfactory result is
obtained. |
 | Presence of systemic diseases, such as diabetes, increases chance of
unsatisfactory recovery. |
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| Treatment |
 | Acyclovir and prednisone produce better results than prednisone and
placebo. |
 | Steroid:
 | There is debate about the efficacy of steroids |
 | Seems to have strong support in the literature for the use of
steroid. |
 | Steroids relieve pain and reduce denervation. |
 | Dosage: Prednisone is 1 mg/ kg of body weight daily for
6 days, tapering
to 0 during the next 4 days. |
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 | Acyclovir (Zovirax):
 | Reduces pain and degree of denervation. |
 | Dosage: 400 mg five times per day for 10 days. |
 | Not FDA approved for this indication. |
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 | Eye Care: artificial tears five times per day and to tape the eye closed
during sleep. |
 | Surgical Decompression: probably not beneficial. |
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| Further reading |
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