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Primitive Neuroectodermal Tumor of the Kidney

DC Field Value Language
dc.contributor.author조, 대성-
dc.contributor.author이, 수형-
dc.contributor.author이, 정환-
dc.contributor.author임, 현이-
dc.contributor.author김, 선일-
dc.contributor.author김, 세중-
dc.date.accessioned2011-12-07T01:53:21Z-
dc.date.available2011-12-07T01:53:21Z-
dc.date.issued2006-
dc.identifier.issn1598-8341-
dc.identifier.urihttp://repository.ajou.ac.kr/handle/201003/4736-
dc.description.abstractPrimitive neuroectodermal tumor(PNET) is a highly aggressive neoplasm belonging to the Ewing family of tumors. PNET with a primary renal localization is very rare, about 50 cases being reported in the literature. We report on a 39-year-old man who presented with an incidentally detected left renal mass and underwent radical nephrectomy with the presumptive diagnosis of renal cell carcinoma. The pathological examination of the tumor revealed PNET of the kidney. Although the tumor was clinically localized, adjuvant chemotherapy was performed. The patient remained free of disease for 38 months after surgery.-
dc.language.isoko-
dc.titlePrimitive Neuroectodermal Tumor of the Kidney-
dc.title.alternative신장에 발생한 원시신경외배엽종양-
dc.typeArticle-
dc.subject.keywordPrimitive neuroectodermal tumor-
dc.subject.keywordKidney-
dc.subject.keywordImmunohistochemistry-
dc.subject.keywordPrognosis-
dc.contributor.affiliatedAuthor조, 대성-
dc.contributor.affiliatedAuthor임, 현이-
dc.contributor.affiliatedAuthor김, 선일-
dc.contributor.affiliatedAuthor김, 세중-
dc.type.localJournal Papers-
dc.citation.titleKorean journal of urological oncology-
dc.citation.volume4-
dc.citation.number2-
dc.citation.date2006-
dc.citation.startPage84-
dc.citation.endPage86-
dc.identifier.bibliographicCitationKorean journal of urological oncology, 4(2). : 84-86, 2006-
dc.relation.journalidJ015988341-
Appears in Collections:
Journal Papers > School of Medicine / Graduate School of Medicine > Urology
Journal Papers > School of Medicine / Graduate School of Medicine > Pathology
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