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Acute Idiopathic Facial Palsy (Bell's Palsy)
Overview
bulletAcute peripheral paralysis of the face produced by a viral immune-mediated disease.
bulletPossible pathogenesis:
bulletAfter a primary infection, herpes simplex virus became latent in the cranial and spinal sensory ganglia.
bulletReactivation of the virus leads to replication of virus within the ganglion cells.
bulletVirus travels up and down the axons, induces an inflammatory response.
bulletResults in segmental demyelination presented as nerve paralysis.
bulletIncidence: between 15 - 40 / 100,000 population per  year
bulletNo evidence of racial predilection
bulletIncidence of Bell's palsy increases with age.
bulletSexual predilection:
bulletAge 10 - 19 years, twice as common in women
bulletAge 40, 1.5 times more common in men.
bulletPregnant women have 3.3 times more risk than nonpregnant women in the same age group.
bulletDiabetic patients: 4.5 times more likely to develop Bell's palsy.
bulletIn 10% of the patients, a positive family history of Bell's palsy is present.
Clinical features
bulletSudden onset
bulletFull extent of the paralysis is usually reached in 1 to 14 days.
bulletEarly phase: retroauricular pain, facial numbness, epiphora, parageusia, decreased tearing, and hyperacusis.
bulletPhysical findings:
bulletPeripheral Facial paresis
bulletHypoesthesia or dysesthesia of cranial nerves V and IX
bulletMotor paresis of cranial nerves IX and X
bulletPapillitis of the tongue.
bulletWhen severe retroauricular pain is present, Ramsay Hunt syndrome has to be considered.
Differential diagnosis of VII weakness
bulletBells' palsy, usually unilateral, 10% bilateral
bulletDifferential of Unilateral Facial weakness
bulletSarcoid
bulletLyme's disease
bulletNeoplasm or mass
bulletOtitis media
bulletTrauma: skull fracture, facial injury
bulletDifferential for bilateral VII palsy
bulletMelkersson-Rosenthal syndrome
bulletRecurrent facial palsy with facial edema,  Unilateral or bilateral
bulletLingua plicata (Scrotal tongue)
bulletMöbius syndrome: Facial paresis with ophthalmoplegia
bulletGuillain-Barré Syndrome
bulletMyasthenia gravis
bulletMotor neuron disease
Prognosis
bulletComplete recovery in 60 to 80%
bulletPrognostic factors:
bulletAge: younger patient has better prognosis.
bulletIncomplete paralysis tends to recover completely.
bulletIf recovery begins between days 10 and 21, a satisfactory result is obtained.
bulletPresence of systemic diseases, such as diabetes, increases chance of unsatisfactory recovery.
Treatment
bulletAcyclovir and prednisone produce better results than prednisone and placebo.
bulletSteroid:
bulletThere is debate about the efficacy of steroids
bulletSeems to have strong support in the literature for the use of steroid.
bulletSteroids relieve pain and reduce denervation.
bulletDosage: Prednisone is 1 mg/ kg of body weight daily for 6 days, tapering to 0 during the next 4 days.
bulletAcyclovir (Zovirax):
bulletReduces pain and degree of denervation.
bulletDosage: 400 mg five times per day for 10 days.
bulletNot FDA approved for this indication.
bulletEye Care: artificial tears five times per day and to tape the eye closed during sleep.
bulletSurgical Decompression: probably not beneficial.
Further reading
bulletFacial paralysis - anatomy, differential - Baylor
bulletAnatomy, Clinical, Differential, bilateral Bell's - Washington Univ
bulletVoluntary control of facial nerves - Univ of Utah
bulletFacial nerve paralysis after surgery - Harvard
bulletOcular management in complete facial paralysis - Harvard
bulletPatient information - Medicine Net

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