拉姆齐·亨特综合征一例报告

M. Dwitasari, D. Seputra
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引用次数: 0

摘要

拉姆齐·亨特综合征(Ramsay Hunt Syndrome, RHS)是一种罕见的疾病,是由潜伏的水痘带状疱疹病毒在膝状神经节重新激活,导致面神经炎症、水肿和压迫引起的。RHS可影响免疫正常和免疫功能低下的患者。RHS的临床表现为带状疱疹性耳廓,表现为耳区或口腔黏膜水疱疹,并伴有周围神经麻痹。我们报告了一位67岁女性患者,自入院前2天起,左侧面部和耳朵出现疱疹性囊泡并伴有同侧周围性面神经麻痹。患者给予阿昔洛韦治疗5天。随访检查显示临床改善满意,囊泡消失,耳痛消失,面部虚弱由House Brackmann III级改善至II级。早期识别和治疗拉姆齐亨特综合征至关重要,因为延迟治疗可能导致后遗症,包括带状疱疹后神经痛和永久性面瘫。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
RAMSAY HUNT SYNDROME: A CASE REPORT
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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