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신경섬유종증과 동반되지 않은 악성 신경집종양

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dc.contributor.author김화미-
dc.contributor.author박동화-
dc.contributor.author김지연-
dc.date.accessioned2022-12-27T02:33:15Z-
dc.date.available2022-12-27T02:33:15Z-
dc.date.issued2012-
dc.identifier.issn0494-4739-
dc.identifier.urihttps://scholarworks.gnu.ac.kr/handle/sw.gnu/23054-
dc.description.abstractMalignant peripheral nerve sheath tumor (MPNST) is a rare entity of all soft tissue sarcomas. It has four different types of glandular, melanocytic, rhabdomyoblastic, and epithelioid. Epithelioid MPNST is composed of predominantly epithelioid cells. In contrast, typical MPNST is consisted of spindle cells, which is arranged in a fascicular or whirling pattern. A 33-old man showed two skin-color to reddish brown protruding nodules on the left thigh. Microscopically, one nodule was made up of epithelioid cell, primarily. In addition, the other nodule was composed of epithelioid cells and spindle cells, which also showed Antoni A and B. Immunohistochemical study showed the cells being positive for S-100 protein (weak and focal) and neuron-specific enolase, and negative for HMB-45, smooth muscle actin. Herein, we report a case of two different forms of malignant nerve sheath tumor on the left thigh, which was not associated with neurofibromatosis-1.-
dc.format.extent5-
dc.language한국어-
dc.language.isoKOR-
dc.publisher대한피부과학회-
dc.title신경섬유종증과 동반되지 않은 악성 신경집종양-
dc.title.alternativeMalignant Peripheral Nerve Sheath Tumor Not Associated with Neurofibromatosis-
dc.typeArticle-
dc.publisher.location대한민국-
dc.identifier.bibliographicCitation대한피부과학회지, v.50, no.4, pp 362 - 366-
dc.citation.title대한피부과학회지-
dc.citation.volume50-
dc.citation.number4-
dc.citation.startPage362-
dc.citation.endPage366-
dc.identifier.kciidART001658619-
dc.description.isOpenAccessN-
dc.description.journalRegisteredClassscopus-
dc.description.journalRegisteredClasskci-
dc.subject.keywordAuthorMalignant nerve sheath tumor-
dc.subject.keywordAuthorMalignant schwannoma-
dc.subject.keywordAuthorPrognosis-
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