頁籤選單縮合
題 名 | Muir-Torre氏徵候群=Muir-Torre Syndrome |
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作 者 | 彭于賓; 李定達; 陳長齡; 王文正; 王鑄軍; | 書刊名 | 中華皮膚科醫學雜誌 |
卷 期 | 18:1 2000.03[民89.03] |
頁 次 | 頁18-22 |
分類號 | 415.78 |
關鍵詞 | Muir-Torre氏徵候群; Muir-Torre syndrome; Sebaceous neoplasms; Visceral malignancy; |
語 文 | 中文(Chinese) |
中文摘要 | Muir-Torre徵候群是一罕見遺傳性疾病合併有惡性腫瘤傾向,並經由不同程度的體顯性遺傳,其定義為皮膚表徵至少有一個皮脂腺腫瘤(腺瘤,上皮瘤,或癌腫)合併至少有一個臟器惡性腫瘤。一位68歲男性病患二年前被診斷為直腸腺癌合併肺及肝轉移,來院求診主訴左耳下方有一皮脂腺腺瘤歷時貳週。吾人報告此罕見病例,並簡介相關文獻。 |
英文摘要 | The Muir-Torre syndrome is an unusual genodermatosis combined with malignant potential. It is a hereditary autosomal dominant disease with a variable degree of penetrance and is defined by the presence of at least a single sebaceous gland tumor (adenoma, epithelioma, or carcinoma) and a minimum of one visceral malignancy. A 68 year-old man was diagnosed as adenocarcinoma of the rectum with metastasis to the lung and liver 2 years ago. He visited our clinic with a lesion of sebaceous adenoma on his left infra-auricular area for two weeks. We herein report this uncommon case and review the literature briefly. |
本系統中英文摘要資訊取自各篇刊載內容。