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克-特综合征中的复发性结节性血管瘤

Recurrent nodular haemangiomas in Klippel-Trénaunay syndrome.

作者信息

Illum N, Winther Nielsen H, Guldhammer Skov B

机构信息

Department of Paediatrics, Hvidovre Hospital, Copenhagen, Denmark.

出版信息

Acta Paediatr. 1992 May;81(5):456-8. doi: 10.1111/j.1651-2227.1992.tb12272.x.

Abstract

A one-year-old child had hypertrophy of the left leg and an unusual constellation of a naevus flammeus and superficial enlarged veins of the trunk together with successive appearance and involution since birth of numerous nodular elements located in the naevus and in the surrounding normal skin. Microscopic examination of these elements showed haemangiomas with capillaries, cavernous channels and lymphangiomatous components. The benign nature of transient nodular elements located to the trunk and the lack of associated visceral vascular malformations in the Klippel-Trénaunay syndrome are documented.

摘要

一名一岁儿童左腿肥大,躯干有鲜红斑痣和浅表扩张静脉,自出生以来,痣内及周围正常皮肤出现并消退了许多结节状病变。对这些病变进行显微镜检查显示,其为含有毛细血管、海绵状血管腔和淋巴管瘤成分的血管瘤。记录了躯干上短暂性结节状病变的良性性质以及Klippel-Trénaunay综合征中无相关内脏血管畸形的情况。

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Recurrent nodular haemangiomas in Klippel-Trénaunay syndrome.克-特综合征中的复发性结节性血管瘤
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