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제 1형 신경섬유종증 환자에서 발생한 악성 섬유성 조직구종

DC FieldValueLanguage
dc.contributor.author김남규-
dc.contributor.author김세훈-
dc.contributor.author김태승-
dc.contributor.author박세호-
dc.contributor.author손승국-
dc.contributor.author유내춘-
dc.contributor.author이강영-
dc.contributor.author조장환-
dc.date.accessioned2015-07-14T17:08:00Z-
dc.date.available2015-07-14T17:08:00Z-
dc.date.issued2004-
dc.identifier.issn1226-0053-
dc.identifier.urihttps://ir.ymlib.yonsei.ac.kr/handle/22282913/112273-
dc.description.abstractType I neurofibromatosis is an autosomal dominant disorder that occurs in 1 of 3,000 births. It is characterized by multiple cutaneous neurofibromas, cafe-au-lait spots of the skin. Patients with neurofibromatosis are at increased risk of developing malignancies, particularly neural crest and other non-neural crest neoplasms. The term ’malignant fibrous histiocytoma’ was first introduced in 1963 to refer to a group of soft tissue tumors characterized by a storiform or cartwheel like growth pattern. Malignant fibrous histiocytomas are the most common type of soft tissue sarcoma that occurs in late adult life. Herein, our recent experienced a case of a malignant fibrous histiocytoma in a 28 year-old female with type I neurofibromatosis is reported, with a review of the literature.-
dc.description.statementOfResponsibilityopen-
dc.format.extent167~170-
dc.relation.isPartOfJOURNAL OF THE KOREAN SURGICAL SOCIETY-
dc.rightsCC BY-NC-ND 2.0 KR-
dc.rights.urihttps://creativecommons.org/licenses/by-nc-nd/2.0/kr/-
dc.title제 1형 신경섬유종증 환자에서 발생한 악성 섬유성 조직구종-
dc.title.alternativeMalignant Fibrous Histiocytoma with Type I Neurofibromatosis-
dc.typeArticle-
dc.contributor.collegeCollege of Medicine (의과대학)-
dc.contributor.departmentDept. of Internal Medicine (내과학)-
dc.contributor.googleauthor박세호-
dc.contributor.googleauthor이강영-
dc.contributor.googleauthor조장환-
dc.contributor.googleauthor김태승-
dc.contributor.googleauthor김세훈-
dc.contributor.googleauthor심효섭-
dc.contributor.googleauthor유내춘-
dc.contributor.googleauthor손승국-
dc.contributor.googleauthor김남규-
dc.admin.authorfalse-
dc.admin.mappingfalse-
dc.relation.journalcodeJ01893-
dc.subject.keywordNeurofibromatosis-
dc.subject.keywordMalignant fibrous histiocytoma-
dc.contributor.alternativeNameKim, Nam Kyu-
dc.contributor.alternativeNameKim, Se Hoon-
dc.contributor.alternativeNameKim, Tai Seung-
dc.contributor.alternativeNamePark, Se Ho-
dc.contributor.alternativeNameSohn, Seung Kook-
dc.contributor.alternativeNameYoo, Nae Choon-
dc.contributor.alternativeNameLee, Kang Young-
dc.contributor.alternativeNameCho, Chang Hwan-
dc.rights.accessRightsfree-
dc.citation.volume67-
dc.citation.number2-
dc.citation.startPage167-
dc.citation.endPage170-
dc.identifier.bibliographicCitationJOURNAL OF THE KOREAN SURGICAL SOCIETY , Vol.67(2) : 167-170, 2004-
Appears in Collections:
1. College of Medicine (의과대학) > Dept. of Pathology (병리학교실) > 1. Journal Papers
1. College of Medicine (의과대학) > Dept. of Surgery (외과학교실) > 1. Journal Papers
1. College of Medicine (의과대학) > Dept. of Internal Medicine (내과학교실) > 1. Journal Papers

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