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Lymphangiomatosis of Bone (A Case Report) : 골의 림프관종증

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dc.contributor.authorChi, Je G.-
dc.contributor.authorYean, Kyung Ma-
dc.contributor.authorAhn, Hya Sup-
dc.contributor.authorLee, Duk Yang-
dc.date.accessioned2009-07-14T09:14:35Z-
dc.date.available2009-07-14T09:14:35Z-
dc.date.issued1986-12-
dc.identifier.citationSeoul J Med, Vol.27 No.4, pp. 355-359-
dc.identifier.issn0582-6802-
dc.identifier.urihttps://hdl.handle.net/10371/5527-
dc.description.abstractLymphangioma of bone is extremely rare disease and characteristically involves
multiple bones, thus justifying the term Iymphangiomatosis. This case report describes a 4
year old boy who came in because of a pathologic fracture after a minor trauma. Cystic
rarefactions were found by bone series, in various sites; both proximal humeri, scapula, clavicle,
rib, both femora and pelvis. Open biopsy revealed a characteristic cavernous lymphangiomas.
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dc.language.isoen-
dc.publisherSeoul National University College of Medicine-
dc.subjectBone-
dc.subjectLymphangioma-
dc.subjectCavernous lymphangioma-
dc.subjectLymphangiectasis-
dc.subjectLymphangiomatosis-
dc.subjectMalformation-
dc.titleLymphangiomatosis of Bone (A Case Report)-
dc.title.alternative골의 림프관종증-
dc.typeSNU Journal-
dc.contributor.AlternativeAuthor지제근-
dc.contributor.AlternativeAuthor연경모-
dc.contributor.AlternativeAuthor안효섭-
dc.contributor.AlternativeAuthor이덕용-
dc.citation.journaltitle서울 의대 잡지-
dc.citation.journaltitle서울 의대 학술지-
dc.citation.journaltitleSeoul Journal of Medicine-
dc.citation.endpage359-
dc.citation.number4-
dc.citation.pages355-359-
dc.citation.startpage355-
dc.citation.volume27-
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