Although some cells appear epithelioid with plump eosinophilic or clear cytoplasm, this malignant neoplasm consists predominantly of pleomorphic cells with eosinophilic fibrillary cytoplasm and brisk mitotic activity that are most consistent with WHO grade IV glioblastoma. s there any focus of necrosis and/or vascular proliferation? Several differential diagnoses need to be ruled out by careful examination of routine HE-stained sections and, perhaps, immunohistochemical stains (GFAP, EMA, AE1). They include choroid plexus carcinoma (AE1, EMA), atypical teratoid/rhabdoid tumor, supratentorial PNET and pleomorphic xanthoastrocytoma (unlikely in the presence of easily seen mitoses).
Although some cells appear epithelioid with plump eosinophilic or clear cytoplasm, this malignant neoplasm consists predominantly of pleomorphic cells with eosinophilic fibrillary cytoplasm and brisk mitotic activity that are most consistent with WHO grade IV glioblastoma. s there any focus of necrosis and/or vascular proliferation? Several differential diagnoses need to be ruled out by careful examination of routine HE-stained sections and, perhaps, immunohistochemical stains (GFAP, EMA, AE1). They include choroid plexus carcinoma (AE1, EMA), atypical teratoid/rhabdoid tumor, supratentorial PNET and pleomorphic xanthoastrocytoma (unlikely in the presence of easily seen mitoses).