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dc.contributor.authorCALAY, Zerrin
dc.contributor.authorComunoglu, Nil
dc.contributor.authorMUESLUEMANOGLU, Mahmut
dc.contributor.authorIlvan, Sennur
dc.contributor.authorCOMUNOGLU, Cem
dc.date.accessioned2021-03-05T21:36:07Z
dc.date.available2021-03-05T21:36:07Z
dc.date.issued2007
dc.identifier.citationComunoglu N., COMUNOGLU C., Ilvan S., CALAY Z., MUESLUEMANOGLU M., "Mammary pseudoangiomatous stromal hyperplasia composed of predominantly giant cells: An unusual variant", BREAST JOURNAL, cilt.13, ss.568-570, 2007
dc.identifier.issn1075-122X
dc.identifier.otherav_d9aa03a5-f6bd-4883-850b-89a16da93e0e
dc.identifier.othervv_1032021
dc.identifier.urihttp://hdl.handle.net/20.500.12627/143551
dc.identifier.urihttps://doi.org/10.1111/j.1524-4741.2007.00508.x
dc.description.abstractPseudoangiomatous stromal hyperplasia (PASH) is a benign proliferative lesion of mammarian stroma that presents as a localized mass. We describe the clinical, radiologic, cytologic, and histopathologic features of a case of PASH with giant cells that presented as a rapidly growing localized mass in the breast in a 32-year-old woman. An unusual feature of our case was the presence of multinucleated giant cells lining pseudovascular spaces and dispersing in collagenous stroma. To the best of our knowledge, this is the second case in the English literature and PASH with predominance of multinucleated giant cells has never been described previously in a female patient.
dc.language.isoeng
dc.subjectOnkoloji
dc.subjectCerrahi Tıp Bilimleri
dc.subjectKadın Hastalıkları ve Doğum
dc.subjectSağlık Bilimleri
dc.subjectİç Hastalıkları
dc.subjectDahili Tıp Bilimleri
dc.subjectTıp
dc.subjectKADIN HASTALIKLARI & DOĞUM
dc.subjectKlinik Tıp (MED)
dc.subjectKlinik Tıp
dc.subjectONKOLOJİ
dc.titleMammary pseudoangiomatous stromal hyperplasia composed of predominantly giant cells: An unusual variant
dc.typeMakale
dc.relation.journalBREAST JOURNAL
dc.contributor.departmentİstanbul Üniversitesi , ,
dc.identifier.volume13
dc.identifier.issue6
dc.identifier.startpage568
dc.identifier.endpage570
dc.contributor.firstauthorID89851


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