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伴有动静脉畸形的卡波西样血管角皮瘤(斯图尔特-布卢法布综合征)。

Kaposiform acro-angiodermatitis with arteriovenous malformation (Stewart-Bluefarb syndrome).

作者信息

König A, Brüngger A, Schnyder U W

机构信息

Department of Dermatology, University Hospital of Zurich, Switzerland.

出版信息

Dermatologica. 1990;181(3):254-7. doi: 10.1159/000247949.

Abstract

A case of acro-angiodermatitis with congenital arteriovenous fistulae (Stewart-Bluefarb syndrome) at the distal right foot in a young man is reported. The lesion evolved slowly from a small dark-red spot existing from birth. Besides mechanical disturbances, the patient's only symptoms were a warmer and somewhat bigger right foot compared to the left nonaffected side. He presented a circumscribed spongy, livid-red coloured angiomatous lesion at the upper part of the distal right foot, also involving the proximal parts of the three middle toes. The diagnosis was based on the clinical aspect and the findings by Doppler ultrasonographic and oscillographic examination. The transcutaneous oxygen pressure showed a marked hypoxia at the edge of the acro-angiodermatitis. Finally, arteriovenous fistulae were demonstrated by arteriography.

摘要

报告了一名年轻男性右足远端患有先天性动静脉瘘(斯图尔特-布卢法布综合征)的肢端血管性皮炎病例。病变从出生时就存在的一个小暗红色斑点开始缓慢演变。除了机械性干扰外,患者唯一的症状是与未受影响的左侧相比,右脚更温暖且稍大。他在右足远端上部出现一个边界清楚的海绵状、青红色血管瘤样病变,也累及三个中趾的近端部分。诊断基于临床症状以及多普勒超声和示波检查结果。经皮氧分压显示肢端血管性皮炎边缘存在明显缺氧。最后,动脉造影证实了动静脉瘘的存在。

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