頁籤選單縮合
題 名 | Behcet's disease之內耳侵犯--病例報告=Inner Ear Involvement in Behcet's Disease--Case Report |
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作 者 | 莊京憲; 楊怡和; | 書刊名 | 中華民國耳鼻喉科醫學會雜誌 |
卷 期 | 33:2 1998.04[民87.04] |
頁 次 | 頁82-85 |
分類號 | 415.933 |
關鍵詞 | Behcet病; 葡萄膜炎; 突發性耳聾; Behcet's disease; Uveitis; Sudden deafness; |
語 文 | 中文(Chinese) |
中文摘要 | Behcet病是一罕見之自體免疫疾病,其臨床特徵以反覆發作之口腔潰瘍,生殖器潰 瘍,眼球葡萄膜炎,及紅斑性結節等症狀為表徵;而內耳受犯之比例則達30%。本科於1995 年經驗1例Behcet病,以單側性突發性耳聾為表現,繼之發生兩耳聽力惡化現象。(中耳醫 誌 1998; 33:180-183。) |
英文摘要 | Behcet's disease is a rare autoimmune disease. Its clinical characters are recurrent oral ulcers, genital ulcers, uveitis and skin lesions such as erythema nodosum. According to the literature, the rate of inner ear involvement is as high as 30%. In 1995, we experienced one case of Behcert's disease with inner ear involvement presenting as unilateral sudden sensorineural hearing loss. Bilateral hearing deterioration were noted in the following one and a half years despite treatment. |
本系統中英文摘要資訊取自各篇刊載內容。