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Extramedullary hematopoiesis at the posterior mediastinum in patient with hereditary spherocytosis: A case report

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dc.contributor.authorYeom, S.Y.-
dc.contributor.authorLim, J.H.-
dc.contributor.authorHan, K.N.-
dc.contributor.authorKang, C.H.-
dc.contributor.authorPark, I.K.-
dc.contributor.authorKim, Y.T.-
dc.date.accessioned2024-07-01T07:04:23Z-
dc.date.available2024-07-01T07:04:23Z-
dc.date.issued2013-04-
dc.identifier.issn2233-601X-
dc.identifier.issn2093-6516-
dc.identifier.urihttps://scholarworks.bwise.kr/cau/handle/2019.sw.cau/74475-
dc.description.abstractThoracic extramedullary hematopoiesis (EMH) is a rare disease entity that is usually associated with hematologic disorders, such as myelodysplastic or hemolytic disease. Because thoracic EMH is usually encountered as a mass during radiologic examinations, it should be differentiated from posterior mediastinal neurogenic tumors. Here, the authors report a case of EMH associated with hereditary spherocytosis.The patient underwent a complete excision by thoracoscopic surgery to differentiate it from other mediastinal tumors. © The Korean Society for Thoracic and Cardiovascular Surgery.-
dc.format.extent3-
dc.language영어-
dc.language.isoENG-
dc.titleExtramedullary hematopoiesis at the posterior mediastinum in patient with hereditary spherocytosis: A case report-
dc.typeArticle-
dc.identifier.doi10.5090/kjtcs.2013.46.2.156-
dc.identifier.bibliographicCitationKorean Journal of Thoracic and Cardiovascular Surgery, v.46, no.2, pp 156 - 158-
dc.description.isOpenAccessY-
dc.identifier.scopusid2-s2.0-84877025931-
dc.citation.endPage158-
dc.citation.number2-
dc.citation.startPage156-
dc.citation.titleKorean Journal of Thoracic and Cardiovascular Surgery-
dc.citation.volume46-
dc.type.docTypeArticle-
dc.publisher.location대한민국-
dc.subject.keywordAuthorHematopoiesis, extramedullary-
dc.subject.keywordAuthorHereditary spherocytosis-
dc.subject.keywordAuthorMediastinal neoplasms-
dc.description.journalRegisteredClassscopus-
dc.description.journalRegisteredClasskci-
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