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Klippel-Trenaunay Syndrome, a Rare Cause of Hematochezia. | LitMetric

Klippel-Trenaunay Syndrome, a Rare Cause of Hematochezia.

Gastroenterology Res

Division of Gastroenterology and Hepatology, SBH Health System, 4422 Third Ave, Bronx, NY 10457, USA.

Published: December 2018

Klippel-Trenaunay syndrome (KTS) is a rare disorder with a wide array of clinical manifestations. It is primarily a disorder of vascular malformations that is classically associated with the development of hemangiomas and venous malformations. Rarely will KTS present with visceral involvement. Venous malformations of the gastrointestinal tract in specific are an exceedingly rare manifestation of KTS. When present, it can result in life-threatening bleeding that is oftentimes difficult to manage. Our case highlights a 53-year-old woman who presented to our clinic with chronic rectal bleeding secondary to KTS.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6306110PMC
http://dx.doi.org/10.14740/gr1092DOI Listing

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