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J Korean Soc Radiol. 2012 Oct;67(4):289-292. English. Case Report. https://doi.org/10.3348/jksr.2012.67.4.289
Kim HY , Chang YW , Lee DH .
Department of Radiology, Soonchunhyang University Hospital, Seoul, Korea. ywchang@schmc.ac.kr
Department of Pediatrics, Soonchunhyang University Hospital, Seoul, Korea.
Abstract

Klippel-Trenaunay-Weber syndrome (KTWS) is a rare congenital disorder, characterized by a cutaneous vascular nevus of the involved extremity, vascular malformations, bone and soft tissue hypertrophy of the extremity. We present the case of an 18-year-old female patient with KTWS, showing a marked rectosigmoid wall thickening and phlebolith, and also variable sized cystic masses in the spleen, as a result of vascular malformations.

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