Abstract

We report a case of Ramsay Hunt syndrome followed by cerebellar encephalitis. A 69-year-old man with concomitant presentation of right severe facial palsy, ipsilateral auricular vesicle and vertigo was referred to our hospital under a diagnosis of Ramsay Hunt syndrome. A high dose of steroid and a conventional dose of acyclovir were administered from the second day of the disease onset. He quickly recovered from the vertigo, but the facial palsy persisted. He also exhibited an ataxic gait several days after the primary treatment. An increase in cell count, protein and VZV Ig-G in the cerebrospinal fluid led to a diagnosis of VZV-associated cerebellitis, even though VZV DNA was negative on PCR. Twice the previous doses of steroid and acyclovir each was administered and thereafter his walking ability improved. Care for central nerve complication should be taken in cases with VZV reactivation.

Full Text
Paper version not known

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call

Disclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.