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직장과 비장의 혈관기형을 동반한 Klippel-Trenaunay-Weber Syndrome: 증례 보고
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| DC Field | Value | Language |
|---|---|---|
| dc.contributor.author | 김하연 | - |
| dc.contributor.author | 장윤우 | - |
| dc.contributor.author | 이동환 | - |
| dc.date.accessioned | 2021-08-12T03:47:58Z | - |
| dc.date.available | 2021-08-12T03:47:58Z | - |
| dc.date.issued | 2012 | - |
| dc.identifier.issn | 1738-2637 | - |
| dc.identifier.issn | 2288-2928 | - |
| dc.identifier.uri | https://scholarworks.bwise.kr/sch/handle/2021.sw.sch/15618 | - |
| dc.description.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. | - |
| dc.format.extent | 4 | - |
| dc.language | 영어 | - |
| dc.language.iso | ENG | - |
| dc.publisher | 대한영상의학회 | - |
| dc.title | 직장과 비장의 혈관기형을 동반한 Klippel-Trenaunay-Weber Syndrome: 증례 보고 | - |
| dc.title.alternative | Rectal and Splenic Vascular Malformation in Klippel-Trenaunay-Weber Syndrome: A Case Report | - |
| dc.type | Article | - |
| dc.publisher.location | 대한민국 | - |
| dc.identifier.bibliographicCitation | 대한영상의학회지, v.67, no.4, pp 289 - 292 | - |
| dc.citation.title | 대한영상의학회지 | - |
| dc.citation.volume | 67 | - |
| dc.citation.number | 4 | - |
| dc.citation.startPage | 289 | - |
| dc.citation.endPage | 292 | - |
| dc.identifier.kciid | ART001704513 | - |
| dc.description.isOpenAccess | N | - |
| dc.description.journalRegisteredClass | kci | - |
| dc.subject.keywordAuthor | Klippel-Trenaunay-Weber Syndrome | - |
| dc.subject.keywordAuthor | Vascular Malformations | - |
| dc.subject.keywordAuthor | Computed Tomography | - |
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Related Researcher
- Chang, Yun Woo
- College of Medicine (Department of Radiology)