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항호중구 세포질 항체 음성인 Churg-Strauss 증후군 1예

DC Field Value Language
dc.contributor.author강희철-
dc.contributor.author이승범-
dc.date.accessioned2015-04-23T17:45:11Z-
dc.date.available2015-04-23T17:45:11Z-
dc.date.issued2010-
dc.identifier.issn2005-6443-
dc.identifier.urihttps://ir.ymlib.yonsei.ac.kr/handle/22282913/103064-
dc.description.abstractChurg-Strauss syndrome is a rare primary vasculitis called allergic granulomatosis angiitis. There is a substantial overlap of symptoms or signs between different vasculitides, so that a diagnosis of any vasculitis can be determined by a combination of clinical symptoms and laboratory tests. We report a case of a 54-year-old woman who had bronchial asthma, eosinophilia, peripheral polyneuropathy, pulmonary infiltrate, maxillary sinusitis, and extravascular eosinophilic infiltration on skin biopsy. So she was diagnosed as having Churg-Strauss syndrome, but she was antineutrophil cytoplasmic antibodies-negative on immunologic study. She had fever and showed cardiac involvement that was presented as cardiomegaly and pulmonary edema at chest radiography and left ventricular hypertrophy on electrocardiography. After steroid therapy, general condition and skin manifestation were rapidly improved-
dc.description.statementOfResponsibilityopen-
dc.format.extent308~313-
dc.languageKorean-
dc.publisher대한가정의학회-
dc.relation.isPartOfKorean Journal of Family Medicine (가정의학회지)-
dc.rightsCC BY-NC-ND 2.0 KR-
dc.rights.urihttps://creativecommons.org/licenses/by-nc-nd/2.0/kr/-
dc.title항호중구 세포질 항체 음성인 Churg-Strauss 증후군 1예-
dc.title.alternativeA Case Report of Anti-Neutrophil Cytoplasmic Antibodies Negative Churg-Strauss Syndrome-
dc.typeArticle-
dc.contributor.collegeCollege of Medicine (의과대학)-
dc.contributor.departmentDept. of Family Medicine (가정의학)-
dc.contributor.googleauthor이승범-
dc.contributor.googleauthor강희철-
dc.contributor.googleauthor최준정-
dc.identifier.doi10.4082/kjfm.2010.31.4.308-
dc.admin.authorfalse-
dc.admin.mappingfalse-
dc.contributor.localIdA00105-
dc.contributor.localIdA02917-
dc.relation.journalcodeJ02007-
dc.identifier.eissn2092-6715-
dc.subject.keywordKikuchi-Fujimoto Disease-
dc.subject.keywordHistiocytic Necrotizing Lymphadenitis-
dc.subject.keywordImmune Thrombocytopenic Purpura-
dc.contributor.alternativeNameKang, Hee Cheol-
dc.contributor.alternativeNameLee, Seung Beom-
dc.contributor.affiliatedAuthorKang, Hee Cheol-
dc.contributor.affiliatedAuthorLee, Seung Beom-
dc.citation.volume31-
dc.citation.number4-
dc.citation.startPage308-
dc.citation.endPage313-
dc.identifier.bibliographicCitationKorean Journal of Family Medicine, Vol.31(4) : 308-313, 2010-
dc.identifier.rimsid35658-
dc.type.rimsART-
Appears in Collections:
1. College of Medicine (의과대학) > Dept. of Family Medicine (가정의학교실) > 1. Journal Papers

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