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克-特综合征:不寻常的磁共振成像特征

Klippel-Trenaunay syndrome: unusual magnetic resonance features.

作者信息

Srivastava D N, Gulati M S, Thulkar S, Berry M

机构信息

Department of Radiodiagnosis, All India Institute of Medical Sciences, New Delhi, India.

出版信息

Australas Radiol. 1998 Feb;42(1):88-9. doi: 10.1111/j.1440-1673.1998.tb00575.x.

Abstract

Klippel-Trenaunay syndrome (KTS) is a congenital vascular abnormality consisting of a cutaneous naevus, varicose veins and bone and soft-tissue hypertrophy affecting one or more limbs. A case is presented here with some unusual associated findings seen on MR that, to the best of the authors' knowledge, has not been reported in the literature. Although colour Doppler in addition to venography is frequently used in demonstration of the KT vein, MRI may well have an important role in complete assessment.

摘要

克-特综合征(KTS)是一种先天性血管异常,由皮肤痣、静脉曲张以及影响一个或多个肢体的骨骼和软组织肥大组成。本文报告了一例在磁共振成像(MR)上发现一些不寻常相关表现的病例,据作者所知,此前文献中尚未有过报道。尽管除了静脉造影外,彩色多普勒常用于显示KT静脉,但MRI在全面评估中可能具有重要作用。

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