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