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dc.contributor.authorReyhan Eğilmez
dc.contributor.authorHandan Aker
dc.contributor.authorRuhiye Cevit
dc.contributor.authorEsin Yıldız
dc.contributor.authorHüseyin Caşkurlu
dc.date.accessioned23.07.201910:49:13
dc.date.accessioned2019-07-23T16:19:41Z
dc.date.available23.07.201910:49:13
dc.date.available2019-07-23T16:19:41Z
dc.date.issued1998
dc.identifier.issn1019-3103
dc.identifier.urihttp://www.trdizin.gov.tr/publication/paper/detail/TmpFMU1qST0=
dc.identifier.urihttps://hdl.handle.net/20.500.12418/985
dc.description.abstractMalignant sweat gland tumors are very rare form of primary tumors of the skin appendage. In this group, malignant chondroid syringoma is the least common variety. Till 1991, less than twenty cases have been reported. We describe a 30-year-old man with malignant chondroid syringoma of his right hand that arose as a painless, slowly enlarging subcutaneous mass. Microscopically, the tumor consisted of a mixture of solid islands of large pleomorphic epithelial tumor cells in the chondromyxoid stroma. There was moderate nuclear atypia and infiltration into the surrounding tissue. Because of the rare occurrence of the malignant chondroid syringoma, it can easily be misdiagnosed.en_US
dc.description.abstractMalignant sweat gland tumors are very rare form of primary tumors of the skin appendage. In this group, malignant chondroid syringoma is the least common variety. Till 1991, less than twenty cases have been reported. We describe a 30-year-old man with malignant chondroid syringoma of his right hand that arose as a painless, slowly enlarging subcutaneous mass. Microscopically, the tumor consisted of a mixture of solid islands of large pleomorphic epithelial tumor cells in the chondromyxoid stroma. There was moderate nuclear atypia and infiltration into the surrounding tissue. Because of the rare occurrence of the malignant chondroid syringoma, it can easily be misdiagnosed.en_US
dc.language.isoengen_US
dc.rightsinfo:eu-repo/semantics/openAccessen_US
dc.subjectOnkolojien_US
dc.titleMalignant chondroid syringoma: a case reporten_US
dc.typeotheren_US
dc.relation.journalTurkish Journal of Canceren_US
dc.contributor.departmentSivas Cumhuriyet Üniversitesien_US
dc.identifier.volume28en_US
dc.identifier.issue4en_US
dc.identifier.endpage192en_US
dc.identifier.startpage189en_US
dc.relation.publicationcategoryDiğeren_US]


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