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Hunt氏综合征也叫膝状神经节综合征,临床上较为少见.现将我们收治的5例结合文献分析报告如下.1 临床资料1.1 一般资料 男1例,女4例;40岁以下2例,40岁以上3例,平均年龄44岁;发病诱因:感冒3例,劳累1例,无诱因1例;病后就诊时间:3天内1例,3～5天3例,7天1例.1.2 主要临床表现 耳痛5例,Hunt氏区疱疹5例(其中面瘫前出疹2例,面瘫后出疹3例),患侧周围性面瘫5例,听力障碍3例,眩晕2例,水平眼震2例,头痛1例,呕吐3例,食欲减退4例,流泪3例,发热1例.
Hunt’s syndrome is also called geniculate syndrome, clinically rare. We will now treat the 5 cases combined with the literature reported as follows.1 Clinical data 1.1 General information Male 1 cases, female 4 cases; 40 years of age in 2 cases , 3 years old over 40 years old, average age 44 years; Incidence of illness: 3 cases of cold, fatigue in 1 case, no incentive in 1 case; sick time after treatment: 1 case within 3 days, 3 to 5 days in 3 cases, 7 days in 1 case. 1.2 The main clinical manifestations of earache in 5 cases, 5 cases of Hunt’s herpes zoster (including 2 cases of facial paralysis before rash, 3 cases of facial palsy after rash), ipsilateral peripheral facial paralysis in 5 cases, 3 cases of hearing impairment, dizziness in 2 cases, level Nystagmus in 2 cases, headache in 1 case, vomiting in 3 cases, loss of appetite in 4 cases, 3 cases of tearing, fever in 1 case.