Young adult with varicosities and recurrent lower gastrointestinal bleeding

Abstract

A 30 years gentleman presented with anaemia since last ten years due to recurrent rectal bleeding. He has had multiple admissions with transfusions in the preceding 10 years without a clear clinical diagnosis. His physical examination revealed gross pallor, prominent veins on the lateral side of the left lower limb with minimal hypertrophy and a hemangiomatous patch over the left buttock. Colonoscopy revealed a few dilated tortuous submucosal vessels in the rectum and sigmoid colon. A MR angiogram showed absent left popliteal vein and angiomatous lesions in the rectum and sigmoid colon. He was diagnosed to have Klippel-Trenaunay syndrome with hemangiomata of the lower gastrointestinal tract causing bleeding. He underwent a low anterior resection with stapled anastomosis, which has effectively controlled his bleeding. Adults with gastrointestinal bleeding due to congenital venous malformations commonly have visible external stigmata, which are often pointers of rare syndromes.

Síndrome Congénito de Klippel-Trenaunay-Weber. Caso Clínico

“…El compromiso vascular gastrointestinal ha sido descrito hasta en un 20 % de los casos, principalmente en colon sigmoide y recto y durante la primera década de vida con carácter intermitente (Sepulveda et al, 2018;Wang et al, 2010). De acuerdo a lo señalado por Gandhi et al (2019) los pacientes con sangrado clínicamente significativo pueden requerir resección intestinal segmentaria. Husmann et al, 2007 reportaron que en el 30 % de los casos, los pacientes con SKTW presentan alteraciones genitourinarias; en nuestro caso, el paciente presentaba malformaciones vasculares escrotales y atrofia testicular izquierda.…”