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dc.contributor.authorBalak, N
dc.contributor.authorKasaroglu, D
dc.contributor.authorKarasu, A
dc.contributor.authorBayindir, C
dc.date.accessioned2021-03-03T10:54:44Z
dc.date.available2021-03-03T10:54:44Z
dc.date.issued1997
dc.identifier.citationBayindir C., Balak N., Karasu A., Kasaroglu D., "Anaplastic pleomorphic xanthoastrocytoma", CHILDS NERVOUS SYSTEM, cilt.13, sa.1, ss.50-56, 1997
dc.identifier.issn0256-7040
dc.identifier.otherav_2543dbd7-da15-4492-b69b-6fff8b22ab50
dc.identifier.othervv_1032021
dc.identifier.urihttp://hdl.handle.net/20.500.12627/29946
dc.identifier.urihttps://doi.org/10.1007/s003810050040
dc.description.abstractA case of anaplastic pleomorphic xanthoastrocytoma (PXA) in a 9-year-old, girl is reported. Histological features of PXAs are cellular pleomorphism of GFAP-positive cells, with intracytoplasmic lipidic vacuoles and a reticulin network, bizarre giant cells, low mitotic activity, and lack of necrosis and of endothelial vascular proliferations. These tumors are generally reported to have a favorable postoperative course. In our case, a poor clinical prognosis and spread of the illness through the CSF was observed. Immunohistochemical features of the tumor, which were histologically anaplastic in nature, were analyzed. There were small foci of necrosis in the sections of the material obtained at the first operation and extensive necrosis in that from the second operation, although the patient had not received radiotherapy between the operations. The presence of necrosis in PXA is an uncommon and significant feature. It predicts the poor prognosis seen in this case, and therefore this report strongly supports the notion that necrosis should automatically exclude a tumor from the PXA category. The histological grade was evaluated as grade 3 (according to the WHO classification).
dc.language.isoeng
dc.subjectÇocuk Sağlığı ve Hastalıkları
dc.subjectNöroloji
dc.subjectCerrahi Tıp Bilimleri
dc.subjectTıp
dc.subjectDahili Tıp Bilimleri
dc.subjectSağlık Bilimleri
dc.subjectCERRAHİ
dc.subjectPEDİATRİ
dc.subjectKlinik Tıp (MED)
dc.subjectKlinik Tıp
dc.subjectKLİNİK NEUROLOJİ
dc.titleAnaplastic pleomorphic xanthoastrocytoma
dc.typeMakale
dc.relation.journalCHILDS NERVOUS SYSTEM
dc.contributor.department, ,
dc.identifier.volume13
dc.identifier.issue1
dc.identifier.startpage50
dc.identifier.endpage56
dc.contributor.firstauthorID118414


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