CC BY-NC-ND 4.0 · Journal of Fetal Medicine 2015; 02(02): 83-86
DOI: 10.1007/s40556-015-0047-x
Brief Communication

Antenatal Diagnosis of Klippel–Trenaunay–Weber Syndrome

Ashutosh Gupta
1   Department of Fetal Medicine and Clinical Geneticist, Max Super Speciality Hospital, West Block, 1 Press Enclave Road, Saket, 110017, New Delhi, India
,
Anjila Aneja
2   Department of Minimal Access & OBGYN, Fortis Memorial Research Institute, Gurgaon, Haryana, India
,
Sanjay Mehta
3   Department of Radiology, Artemis Health Institute, Gurgaon, Haryana, India
,
Pankaj Saini
3   Department of Radiology, Artemis Health Institute, Gurgaon, Haryana, India
› Author Affiliations

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.



Publication History

Received: 20 March 2015

Accepted: 21 July 2015

Article published online:
08 May 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/)

Thieme Medical and Scientific Publishers Pvt. Ltd.
A-12, 2nd Floor, Sector 2, Noida-201301 UP, India