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克-特-韦综合征的一种罕见变异型。

An unusual variant of Klippel-Trenaunay-Weber syndrome.

作者信息

Belovic B, Nethercott J, Donsky H J

出版信息

Can Med Assoc J. 1974 Sep 7;111(5):439-41.

Abstract

The association of soft tissue and bony overgrowth, varicose veins and port-wine nevus is known as Klippel-Trenaunay-Weber syndrome. An unusual case of a young woman with this syndrome is presented. In addition to the classic features she had face swelling, bilateral limb involvement and an infected cutaneous lymphangioma. No evidence of arteriovenous fistula was demonstrated. In contrast to an abnormal lymphatic system the deep veins of the limbs were normal. Unilateral lung lesions were demonstrated which have not been described previously in such cases.

摘要

软组织和骨过度生长、静脉曲张与葡萄酒色斑痣相关联被称为克-特-韦综合征。本文介绍了一名患有该综合征的年轻女性的罕见病例。除了典型特征外,她还出现面部肿胀、双侧肢体受累以及皮肤淋巴管瘤感染。未发现动静脉瘘的证据。与异常的淋巴系统不同,四肢的深静脉是正常的。还发现了单侧肺部病变,此前此类病例中尚未有过相关描述。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c939/1947783/b8290e0519e4/canmedaj01589-0051-a.jpg

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