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伴有动静脉淋巴畸形的克-特综合征:一种罕见表现

Klippel-Trenaunay Syndrome with Arterio-veno-lymphatic Malformation: A Rare Presentation.

作者信息

Supekar Bhagyashree B, Chopkar Apoorva D, Wankhade Vaishali H, Singh Rajesh Pratap, Bhat Dharitri Mukund, Suresh Parvathy

机构信息

Department of Dermatology, Venereology and Leprology, Government Medical College and Hospital, Nagpur, Maharashtra, India.

Department of Pathology, Government Medical College and Hospital, Nagpur, Maharashtra, India.

出版信息

Indian Dermatol Online J. 2020 May 10;11(3):404-408. doi: 10.4103/idoj.IDOJ_220_19. eCollection 2020 May-Jun.

Abstract

Klippel-Trenaunay syndrome (KTS) is a rare disorder characterized by triad of vascular malformations, varicose veins, and bony or soft tissue hypertrophy involving an extremity. Port wine stain is the most common vascular malformation associated with this syndrome. Various other rare vascular malformations described are angiokeratomas, angiokeratoma circumscriptum naeviformae, angiodermatitis, etc. This is the first instance, to the best of our knowledge, describing the capillary, venous, and lymphatic malformations in a same case of KTS.

摘要

克-特综合征(KTS)是一种罕见的疾病,其特征为累及一个肢体的血管畸形、静脉曲张以及骨骼或软组织肥大三联征。葡萄酒色斑是与此综合征相关的最常见血管畸形。所描述的其他各种罕见血管畸形包括血管角皮瘤、痣样局限性血管角皮瘤、血管性皮炎等。据我们所知,这是首次在同一例KTS中描述毛细血管、静脉和淋巴管畸形。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f500/7367591/b6ecc24595df/IDOJ-11-404-g001.jpg

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