RAMSAY HUNT SYNDROME: A CASE REPORT

Authors

  • Made Ayu Dessy Dwitasari Department of Neurology, Bhakti Rahayu Hospital, Tabanan, Bali, Indonesia
  • Desak Made Cittarasmi Saraswati Seputra Internship Doctor, Bhakti Rahayu Hospital, Tabanan, Bali, Indonesia

DOI:

https://doi.org/10.21776/ub.mnj.2023.009.01.15

Keywords:

Ramsay Hunt Syndrome, Herpes Zoster Oticus, Facial Paralysis

Abstract

Ramsay Hunt Syndrome (RHS) is a rare disease caused by reactivation of latent Varicella Zoster Virus in the geniculate ganglion which lead to inflammation, edema, and compression of facial nerve. RHS may affect both immunocompetent and immunocompromised patient. Clinical manifestation of RHS include herpes zoster oticus that manifest as vesicular rash on auricular area or oral mucosa in combination with peripheral nerve palsy. We reported a 67-years-old female patient with herpetic vesicle on left side of face and ear accompanied with ipsilateral peripheral facial paralysis since 2 days before admission. Patient was treated with acyclovir for 5 days. Follow up examination showed satisfying clinical improvement with disappearance of vesicles and otalgia, as well as facial weakness improvement from House Brackmann grade III to grade II. Early recognition and treatment of Ramsay Hunt Syndrome is crucial as delay of treatment may lead to sequelae, including postherpetic neuralgia and permanent facial paralysis.

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Published

2022-12-20

How to Cite

Dwitasari, M. A. D., & Seputra, D. M. C. S. (2022). RAMSAY HUNT SYNDROME: A CASE REPORT. MNJ (Malang Neurology Journal), 9(1), 70–72. https://doi.org/10.21776/ub.mnj.2023.009.01.15

Issue

Section

Case Report