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DOI: 10.1007/s40556-015-0047-x
Antenatal Diagnosis of Klippel–Trenaunay–Weber Syndrome

Abstract
Klippel–Trenaunay–Weber syndrome (KTWS) is a rare congenital disease characterized by cutaneous hemangiomas, soft tissue, and bone hypertrophy. It may be associated with arteriovenous malformation involving deeper pelvic organs. We present a prenatally-diagnosed case of KTWS identified at 26 weeks. Antenatal ultrasound identified subcutaneous hemangioma with soft tissue hypertrophy with unilateral hypertrophy of the lower extremity with right renal hydronephrosis. During the rest antenatal period, KTWS did not deteriorate and was not complicated by acute enlargement and sequestration and Kasabach–Merritt syndrome.
Publikationsverlauf
Eingereicht: 20. März 2015
Angenommen: 21. Juli 2015
Artikel online veröffentlicht:
08. Mai 2023
© 2015. Society of Fetal Medicine. This is an open access article published by Thieme under the terms of the Creative Commons Attribution-NonDerivative-NonCommercial-License, permitting copying and reproduction so long as the original work is given appropriate credit. Contents may not be used for commercial purposes, or adapted, remixed, transformed or built upon. (https://creativecommons.org/licenses/by-nc-nd/4.0/)
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