Klippel-Trenaunay syndrome (KTS) is a rare congenital disorder and is essentially a disorder of capillary, venous, and lymphatic malformations. Hematochezia is the most common symptom associated with intestinal hemangiomatosis and remains one of the life-threatening emergencies in KTS. We reported one patient of KTS presented with rectal bleeding and severe anemia who was successfully managed by sphincter-saving operation.
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Isolated Colorectal Involvement in Klippel-Trenaunay Syndrome: A Case of Extensive Vascular Malformation Nurbek Ilyassov, Yerzhan Shayakhmetov, Anuar Abdikarimov, Erlan Nurgaliev, Saken Saberbekov, Rakymzhan Aralbayev, Aiman Tokusheva, Vitaliy Kalina International Medical Case Reports Journal.2025; Volume 18: 997. CrossRef
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Rectal and Splenic Vascular Malformation in Klippel-Trenaunay-Weber Syndrome: A Case Report Ha Youn Kim, Yun Woo Chang, Dong Hwan Lee Journal of the Korean Society of Radiology.2012; 67(4): 289. CrossRef