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dc.contributor.author명기범*
dc.contributor.author최혜영*
dc.contributor.author최유원*
dc.date.accessioned2016-08-28T12:08:09Z-
dc.date.available2016-08-28T12:08:09Z-
dc.date.issued2011*
dc.identifier.issn1013-9087*
dc.identifier.otherOAK-7891*
dc.identifier.urihttps://dspace.ewha.ac.kr/handle/2015.oak/221890-
dc.description.abstractDermatofibrosarcoma protuberans (DFSP) is a slowly growing dermal spindle cell tumor and its myxoid variant, a rare type of DFSP, is characterized by extensive myxoid degeneration. We present the case of a 69-year-old woman with a multinodular reddish plaque on her trunk. Histopathologically, the tumor was located in the dermis and consisted of uniform spindle-shaped cells, showing strongly positive reaction for CD34, and negative for both S-100 and desmin. In addition to the typical storiform pattern, prominent myxoid stromal changes were demonstrated. Herein, we report an interesting case of myxoid DFSP, rarely reported in the dermatology literature.*
dc.languageEnglish*
dc.titleA case of myxoid dermatofibrosarcoma protuberans*
dc.typeArticle*
dc.relation.issue3*
dc.relation.volume23*
dc.relation.indexSCIE*
dc.relation.indexSCOPUS*
dc.relation.indexKCI*
dc.relation.startpage379*
dc.relation.lastpage381*
dc.relation.journaltitleAnnals of Dermatology*
dc.identifier.doi10.5021/ad.2011.23.3.379*
dc.identifier.wosidWOS:000294040800020*
dc.identifier.scopusid2-s2.0-80052090356*
dc.author.googleHong Y.J.*
dc.author.googleChoi Y.W.*
dc.author.googleMyung K.B.*
dc.author.googleChoi H.Y.*
dc.contributor.scopusid명기범(7006220296)*
dc.contributor.scopusid최혜영(55724363200)*
dc.contributor.scopusid최유원(7404777738)*
dc.date.modifydate20231120161531*
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의과대학 > 의학과 > Journal papers
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