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dc.contributor.author명기범*
dc.contributor.author최혜영*
dc.date.accessioned2018-06-02T08:14:40Z-
dc.date.available2018-06-02T08:14:40Z-
dc.date.issued2003*
dc.identifier.issn0494-4739*
dc.identifier.otherOAK-17390*
dc.identifier.urihttps://dspace.ewha.ac.kr/handle/2015.oak/244223-
dc.description.abstractGranulomatous pigmented purpuric dermatosis was first described by Saito and Matsuoka in 1996. Clinically, the lesions manifest purpuric and petechial brown pigmented macules as a result of hemosiderin deposits. Histopathologically, it is characterized by lymphocytic perivascular infiltrate limited to the papillary dermis with extravasated red blood cells and hemosiderin deposition, accompanied by granulomatous infiltration. We report our experience of a case which presented a clinical picture of pigmented purpuric dermatosis and histologically granulomatous inflammation.*
dc.languageKorean*
dc.titleA Case of Granulomatous Pigmented Purpuric Dermatosis*
dc.typeArticle*
dc.relation.issue11*
dc.relation.volume41*
dc.relation.indexSCOPUS*
dc.relation.indexKCI*
dc.relation.startpage1530*
dc.relation.lastpage1533*
dc.relation.journaltitleKorean Journal of Dermatology*
dc.identifier.scopusid2-s2.0-0742306008*
dc.author.googleKim S.Y.*
dc.author.googleKim J.S.*
dc.author.googleKim M.H.*
dc.author.googleChoi H.Y.*
dc.author.googleMyung K.B.*
dc.contributor.scopusid명기범(7006220296)*
dc.contributor.scopusid최혜영(55724363200)*
dc.date.modifydate20231116122502*
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의과대학 > 의학과 > Journal papers
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