A Case of Ramsay Hunt Syndrome Followed by Cerebellar Encephalitis

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منابع مشابه

[A case of Ramsay Hunt syndrome].

We describe a clinical case of RH syndrome (Auricular Herpes zoster, facial paralysis, hearing loss).

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A Pediatric Case of Ramsay Hunt Syndrome

Ramsay Hunt syndrome (RHS) is characterized by facial paralysis, inner ear dysfunction, periauricular pain, and herpetiform vesicles. The reported incidence in children is 2.7/100,000. The pathogenesis involves the reactivation of latent varicella zoster virus (VZV) in the geniculate ganglion of the facial nerve. The recovery rate is better in children than in adults. This paper discusses a 12-...

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A Case of Ramsay Hunt Syndrome Complicated by Cerebellitis

Cerebellitis associated with herpes zoster has rarely been observed. We report here a 76-year-old man who had a history of anterior resection for sigmoid colon cancer and presented during chemotherapy with vesicular rash of the left ear, neuralgic pain in the postauricular area, and ataxic gait. After a while, he developed left peripheral facial palsy, fever, aggravated gait ataxia, and prolong...

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Ramsay Hunt syndrome

The strict definition of the Ramsay Hunt syndrome is peripheral facial nerve palsy accompanied by an erythematous vesicular rash on the ear (zoster oticus) or in the mouth. J Ramsay Hunt, who described various clinical presentations of facial paralysis and rash, also recognised other frequent symptoms and signs such as tinnitus, hearing loss, nausea, vomiting, vertigo, and nystagmus. He explain...

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Atypical Ramsay Hunt syndrome.

Ramsay Hunt syndrome (RHS) is the reactivation of herpes zoster in the geniculate ganglion and typically presents the triad of ipsilateral peripheral type facial paralysis, ear pain, and erythematous vesicles in the external auditory canal and auricle. However, some unusual variants may occur. Here we present a patient of atypical RHS with uncommonly extensive dermatomal involvement of cranial ...

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ژورنال

عنوان ژورنال: Practica Oto-Rhino-Laryngologica

سال: 2004

ISSN: 1884-4545,0032-6313

DOI: 10.5631/jibirin.97.775