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dc.contributor.authorGokce, Müge
dc.contributor.authorAytac, Selin
dc.contributor.authorAltan, Ilhan
dc.contributor.authorUnal, Sule
dc.contributor.authorTuncer, Murat
dc.contributor.authorGumruk, Fatma
dc.contributor.authorCetin, Mualla
dc.date.accessioned2019-12-10T10:39:14Z
dc.date.available2019-12-10T10:39:14Z
dc.date.issued2012
dc.identifier.issn1817-1745
dc.identifier.urihttps://doi.org/10.4103/1817-1745.106482
dc.identifier.urihttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC3611913/
dc.identifier.urihttp://hdl.handle.net/11655/14105
dc.description.abstractCentral nervous system leukemia may present in different ways. However, intraparenchymal mass is extremely rare in childhood leukemia. Herein, we report a boy who presented with right hemiparesis and anisocoria 1 year after the cessation of the chemotherapy protocol for acute lymphoblastic leukemia. Cranial imaging demonstrated an extensive mass located in the anterior white matter of left frontal lobe, and cerebrospinal fluid examination revealed concomitant lymphoblasts. Immunohistochemical staining of the biopsy material showed neoplastic cells with positive CD10 and TdT. Complete remission was achieved with chemotherapy alone for a duration of 2 years.
dc.relation.isversionof10.4103/1817-1745.106482
dc.rightsinfo:eu-repo/semantics/openAccess
dc.titleIntracerebral Metastasis In Pediatric Acute Lymphoblastic Leukemia: A Rare Presentation
dc.typeinfo:eu-repo/semantics/article
dc.relation.journalJournal of Pediatric Neurosciences
dc.contributor.departmentÇocuk Sağlığı ve Hastalıkları
dc.identifier.volume7
dc.identifier.issue3
dc.identifier.startpage208
dc.identifier.endpage210
dc.description.indexPubMed


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