DSpace at EWHA: Rectal Involvement of klippel-trenaunay syndrome

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DC Field	Value	Language
dc.contributor.author	박응범	*
dc.date.accessioned	2016-08-28T11:08:15Z	-
dc.date.available	2016-08-28T11:08:15Z	-
dc.date.issued	2009	*
dc.identifier.issn	1229-8670	*
dc.identifier.other	OAK-13416	*
dc.identifier.uri	https://dspace.ewha.ac.kr/handle/2015.oak/229415	-
dc.description.abstract	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. © 2009 The Korean Society of Coloproctology.	*
dc.language	English	*
dc.title	Rectal Involvement of klippel-trenaunay syndrome	*
dc.type	Article	*
dc.relation.issue	1	*
dc.relation.volume	25	*
dc.relation.index	SCOPUS	*
dc.relation.startpage	52	*
dc.relation.lastpage	55	*
dc.relation.journaltitle	Journal of the Korean Society of Coloproctology	*
dc.identifier.doi	10.3393/jksc.2009.25.1.52	*
dc.identifier.scopusid	2-s2.0-77953415236	*
dc.author.google	Cheon S.-H.	*
dc.author.google	Lee S.-H.	*
dc.author.google	Park E.-B.	*
dc.contributor.scopusid	박응범(56059292000)	*
dc.date.modifydate	20240423081003	*