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dc.contributor.authorBİLGİÇ, Mebrure Bilge
dc.contributor.authorOzger, Harzem
dc.contributor.authorUzuner, Esen Gul
dc.contributor.authorDemiryont, Misten
dc.date.accessioned2022-02-18T10:02:26Z
dc.date.available2022-02-18T10:02:26Z
dc.date.issued2008
dc.identifier.citationUzuner E. G. , Demiryont M., BİLGİÇ M. B. , Ozger H., "Acral myxoinflammatory fibrablastic sarcoma: Report of six cases", TURKISH JOURNAL OF PATHOLOGY, cilt.24, sa.1, ss.44-49, 2008
dc.identifier.othervv_1032021
dc.identifier.otherav_768148d2-735f-432d-a73f-0ed870b6b451
dc.identifier.urihttp://hdl.handle.net/20.500.12627/178471
dc.description.abstractAcral myxoinfl a minatory fibroblastic sarcoma was first described in 1998. The tumor typically involves distal extremities; especially fingers and toes. It is usually located in subcutaneous tissue. The age range is broad (mean age 40). The size of tumor varies between 1-8 cm. Microscopically, itnyxold and hyaline zones are characteristic. Inflammatory cells are abundant and there are large cells resembling Reed Sternberg or ganglion cells and multi yactoilated cells having lipoblast-like appearance.
dc.language.isoeng
dc.subjectBiochemistry (medical)
dc.subjectPATOLOJİ
dc.subjectBiyoloji ve Biyokimya
dc.subjectYaşam Bilimleri (LIFE)
dc.subjectTıp
dc.subjectSağlık Bilimleri
dc.subjectTemel Tıp Bilimleri
dc.subjectBiyokimya
dc.subjectCerrahi Tıp Bilimleri
dc.subjectPatoloji
dc.subjectYaşam Bilimleri
dc.subjectTemel Bilimler
dc.subjectHistology
dc.subjectPathology and Forensic Medicine
dc.subjectHealth Sciences
dc.titleAcral myxoinflammatory fibrablastic sarcoma: Report of six cases
dc.typeMakale
dc.relation.journalTURKISH JOURNAL OF PATHOLOGY
dc.contributor.departmentİstanbul Teknik Üniversitesi , ,
dc.identifier.volume24
dc.identifier.issue1
dc.identifier.startpage44
dc.identifier.endpage49
dc.contributor.firstauthorID3375473


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