Klippel-Trenaunay Syndrome, a Rare Cause of Hematochezia

被引：4

作者：

Then, Eric Omar ^{[1
]}

Ofosu, Andrew ^{[2
]}

Rawla, Prashanth ^{[3
]}

Sunkara, Tagore ^{[2
]}

Gaduputi, Vinaya ^{[1
]}

机构：

[1] SBH Hlth Syst, Div Gastroenterol & Hepatol, 4422 Third Ave, Bronx, NY 10457 USA

[2] Mt Sinai Hosp, Brooklyn Hosp Ctr, Div Gastroenterol & Hepatol, 121 Dekalb Ave, Brooklyn, NY 11201 USA

[3] Mem Hosp Martinsville & Henry Cty, Dept Internal Med, 320 Hosp Dr, Martinsville, VA 24115 USA

来源：

GASTROENTEROLOGY RESEARCH | 2018年 / 11卷 / 06期

关键词：

Hematochezia; Rectal bleeding; Klippel-Trenaunay syndrome; Anemia; Hemangioma;

D O I：

10.14740/gr1092

中图分类号：

R57 [消化系及腹部疾病];

学科分类号：

摘要：

Klippel-Trenaunay syndrome (KTS) is a rare disorder with a wide array of clinical manifestations. It is primarily a disorder of vascular malformations that is classically associated with the development of hemangiomas and venous malformations. Rarely will KTS present with visceral involvement. Venous malformations of the gastrointestinal tract in specific are an exceedingly rare manifestation of KTS. When present, it can result in life-threatening bleeding that is often times difficult to manage. Our case highlights a 53-year-old woman who presented to our clinic with chronic rectal bleeding secondary to KTS.

引用

页码：426 / 429

页数：4

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