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. 2018 Jan;23(1):18–22. doi: 10.17712/nsj.2018.1.20160543

Table 1.

Pathological types for all cases of the study.

Histology type KFSH-D (%)
Pilocytic Astrocytoma (WHO 1) (infra-tentorial) 11 (7.3)
Pilocytic Astrocytoma (WHO 1) (Optic pathway glioma) 3 (2)
Diffuse Astrocytoma (WHO 11) 7 (4.6)
Anaplastic Astrocytoma (WHO 111) 13 (8.7)
Oligodendroglioma (WHO 11) 4 (2.7)
Anaplastic oligodendrioglioma (WHO 111) 9 (6)
Mixed glioma (WHO 11) 2 (1.3)
Mixed glioma (WHO111) 2 (1.3)
Diffuse brain stem glioma 9 (6)
GBM (WHO 1V) 48 (32)
Gliosarcoma (WHO 1V) 2 (1.3)
Ependymoma (WHO 11 and WHO 111) 11 (7.3)
PNET/MB (WHO 1V) (Infra-tentorial) 16 (10.7)
PNET (WHO 1V) (supra-tentorial) 2 (1.3)
Pineoblastoma l tumors (WHO 1V) 2 (1.3)
Choroid plexus papilloma/ carcinoma 3 (2)
PXA (WHO 11 and 111) 3 (2)
Central Neurocytoma (WHO 11) 2 (1.3)
Total 149 (100)

GBM - Glioblastoma multiforme, PNET - Primitive Neuroectrodermal Tumor, MB - Medulloblastoma, PXA-Pleomorphic Xanthoastrocytoma