頁籤選單縮合
題名 | Hopf氏疣狀肢端角化症=Acrokeratosis verruciformis of Hopf |
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作者姓名(中文) | 江建平; 林汝宇; 汪經堯; 王偉銘; | 書刊名 | 中華皮膚科醫學雜誌 |
卷期 | 18:1 2000.03[民89.03] |
頁次 | 頁37-42 |
分類號 | 415.723 |
關鍵詞 | Hopf氏疣狀肢端角化症; Acrokeratosis verruciformis of Hopf; Genodermatosis; Darier's disease; |
語文 | 中文(Chinese) |
中文摘要 | Hopf氏疣狀肢端角化症為一種自體顯性遺傳之罕見皮膚疾患。本病例報告一位十九歲男性病患自幼年就在手背及腳背呈現許多疣狀突起,而身上亦有淺色丘疹散在地分佈於前側軀幹;左側頸部則有一斑塊其上散佈有一些深色丘疹。經過多處切片及連續切面檢查,在病理下可見過度角化、顆粒層增生及乳突狀增生形成典型的「教堂尖塔」樣變化,但並未發現不完全角化及角化不良的情形。因此,吾人確立Hopf氏疣狀肢端角化症之診斷並對文獻稍作回顧。 |
英文摘要 | Acrokeratosis verruciformis of Hopf is a rare genodermatosis as an autosomal dominant trait. We herein report a 19-year-old male patient who presented with multiple discrete warty papules on his dorsal hands and feet since early childhood. Besides, he also had quite a few small hypopigmented papules scattered throughout his anterior trunk and some hyperpigmetned papules located on a patch over his lft neck. Multiple skin biopsies with serial sections were performed. Histpathology showed hyperkeratosis, hypergranulosis and papillomatosis with a typical picture of “church spires”, but no dyskeratosis or parakeratosis was found. Adiagnosis of acrokeratosis verruciformis was made and the literature was reviewed. |
本系統之摘要資訊系依該期刊論文摘要之資訊為主。