一名患有克-特综合征患者的食管鳞状细胞癌。

Squamous cell carcinoma of the oesophagus in a patient with Klippel-Trenaunay syndrome.

作者信息

Bujanda L, Sánchez A, Vicente J M, Sánchez A, Fernández Cantón G F, Olagoitia J M, Iriondo C, Fernández de Luco M A, Muñoz C

机构信息

Department of Gastroenterology, San Eloy Hospital, Baracaldo, Spain.

出版信息

Eur J Gastroenterol Hepatol. 2001 Sep;13(9):1107-10. doi: 10.1097/00042737-200109000-00019.

DOI:10.1097/00042737-200109000-00019

PMID:11564964

Abstract

The Klippel-Trenaunay syndrome (KTS) is a rare disorder characterized by a triad of port-wine stains, varicose veins, and bony or soft tissue hypertrophy of one extremity. Digestive bleeding is the most commonly observed gastrointestinal manifestation. In rare cases, the syndrome is associated with malignancies. We report the case of a 38-year-old woman with KTS and dysphagia caused by an oesophageal squamous cell carcinoma.

摘要

克-特综合征（KTS）是一种罕见的疾病，其特征为三联征，即葡萄酒色斑、静脉曲张以及一侧肢体的骨或软组织肥大。消化道出血是最常见的胃肠道表现。在罕见情况下，该综合征与恶性肿瘤有关。我们报告一例38岁患有克-特综合征且因食管鳞状细胞癌导致吞咽困难的女性病例。