Klippel-Trenaunay-Weber Syndrome – A Rare Case with Visceral Manifestation and Thrombosed Marginal Vein of Servelle

Authors

  • Muhammad Imran Ibrahim Combined Military Hospital/National University of Medical Science (NUMS) Rawalpindi Pakistan
  • Leena Hussain Awan Combined Military Hospital/National University of Medical Science (NUMS) Rawalpindi Pakistan
  • Babar Khan Combined Military Hospital/National University of Medical Science (NUMS) Rawalpindi Pakistan
  • Koukab Javed Combined Military Hospital/National University of Medical Science (NUMS) Rawalpindi Pakistan
  • Syeda Mariam Zehra Combined Military Hospital/National University of Medical Science (NUMS) Rawalpindi Pakistan
  • Mariam Hussain Combined Military Hospital/National University of Medical Science (NUMS) Rawalpindi Pakistan

DOI:

https://doi.org/10.51253/pafmj.v72i3.6694

Keywords:

Hemihypertrophy, Klippel-trenaunay-weber syndrome, Marginal vein of servelle, Port-wine stain

Abstract

Klippel-Trenaunay-Weber syndrome is a rare congenital syndrome characterized by capillary, venous or lymphatic
malformation and hemihypertrophy. Only 1000 cases of this syndrome have been reported in the literature. A rare case of this syndrome is presented here, who presented with its visceral and vascular complications and was diagnosed for the first time.

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Published

08-07-2022

Issue

Vol. 72 No. 3 (2022): June

Section

Case Reports

How to Cite

1.
Ibrahim MI, Hussain Awan L, Khan B, Javed K, Mariam Zehra S, Hussain M. Klippel-Trenaunay-Weber Syndrome – A Rare Case with Visceral Manifestation and Thrombosed Marginal Vein of Servelle. Pak Armed Forces Med J [Internet]. 2022 Jul. 8 [cited 2024 Dec. 27];72(3):1142-43. Available from: https://pafmj.org/PAFMJ/article/view/6694
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