Pereira Flávia P, Guskuma Marcos H, Luvizuto Eloá R, Faco Eduardo F S, Magro-Filho Osvaldo, Hochuli-Vieira Eduardo
Department of Surgery and Integrated Clinic, UNESP, Araçatuba Dental School, São Paulo, Brazil.
J Craniofac Surg. 2011 Sep;22(5):1961-3. doi: 10.1097/SCS.0b013e31822ea828.
The Ramsay Hunt syndrome is a rare disease caused by an infection of the geniculate ganglion by the varicella-zoster virus. The main clinical features of the syndrome are as follows: Bell palsy unilateral or bilateral, vesicular eruptions on the ears, ear pain, dizziness, preauricular swelling, tingling, tearing, loss of taste sensation, and nystagmus. We describe a 23-year-old white woman, who presented with facial paralysis on the left side of the face, pain, fever, ear pain, and swelling in the neck and auricular region on the left side. She received appropriate treatment with acyclovir, vitamin B complex, and CMP nucleus. After 30 days after presentation, the patient did not show any signs or symptoms of the syndrome. At follow-up at 1 year, she showed no relapse of the syndrome.
拉姆齐·亨特综合征是一种由水痘-带状疱疹病毒感染膝状神经节引起的罕见疾病。该综合征的主要临床特征如下：单侧或双侧贝尔面瘫、耳部水疱疹、耳痛、头晕、耳前肿胀、刺痛、流泪、味觉丧失和眼球震颤。我们描述了一名23岁的白人女性，她出现左侧面部麻痹、疼痛、发热、耳痛以及左侧颈部和耳部区域肿胀。她接受了阿昔洛韦、复合维生素B和胞磷胆碱的适当治疗。就诊30天后，患者未出现该综合征的任何体征或症状。在1年的随访中，她未出现该综合征的复发。
