Case Report

Three cases with Klippel-Trenaunay syndrome and treatment options

Volume: 6 Number: 2 March 4, 2020
EN

Three cases with Klippel-Trenaunay syndrome and treatment options

Abstract

Klippel-Trenaunay syndrome (KTS) is a rare congenital anomaly characterized by capillary malformations, soft tissue and bone hypertrophy and varicosities. The presence of at least two of the three clinical conditions is sufficient for the diagnosis of KTS. Early diagnosis and treatment are important because of possible serious complications such as deep vein thrombosis and pulmonary embolism. Venous system aplasia and/or hypoplasia might be observed in KTS. Therefore, deep venous system must be evaluated definitely before determining the treatment strategy. It's herein presented our conservative and surgical treatment applications in three KTS patients. 

Keywords

References

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Details

Primary Language

English

Subjects

Cardiovascular Surgery

Journal Section

Case Report

Publication Date

March 4, 2020

Submission Date

November 8, 2018

Acceptance Date

October 16, 2019

Published in Issue

Year 2020 Volume: 6 Number: 2

AMA
1.Çelik E, Alat İ. Three cases with Klippel-Trenaunay syndrome and treatment options. Eur Res J. 2020;6(2):169-172. doi:10.18621/eurj.480577