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직장과 비장의 혈관기형을 동반한 Klippel-Trenaunay-Weber Syndrome: 증례 보고Rectal and Splenic Vascular Malformation in Klippel-Trenaunay-Weber Syndrome: A Case Report
- Other Titles
- Rectal and Splenic Vascular Malformation in Klippel-Trenaunay-Weber Syndrome: A Case Report
- Issue Date
- 2012
- Publisher
- 대한영상의학회
- Keywords
- Klippel-Trenaunay-Weber Syndrome; Vascular Malformations; Computed Tomography
- Citation
- 대한영상의학회지, v.67, no.4, pp 289 - 292
- Pages
- 4
- Journal Title
- 대한영상의학회지
- Volume
- 67
- Number
- 4
- Start Page
- 289
- End Page
- 292
- ISSN
- 1738-2637
2288-2928
- 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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Related Researcher
- Chang, Yun Woo
- College of Medicine (Department of Radiology)