{Reference Type}: Journal Article
{Title}: Immunohistochemical and molecular genetic study on epithelioid glioblastoma: Series of seven cases with review of literature.
{Author}: Khanna G;Pathak P;Suri V;Sharma MC;Chaturvedi S;Ahuja A;Bhardwaj M;Garg A;Sarkar C;Sharma R;
{Journal}: Pathol Res Pract
{Volume}: 214
{Issue}: 5
{Year}: May 2018
{Factor}: 3.309
{DOI}: 10.1016/j.prp.2018.03.019
{Abstract}: Epithelioid glioblastoma (e-gbm) is a recently described variant of glioblastoma (GBM) which is associated with short survival and now added as a provisional entity to WHO 2016 classification of CNStumors. About half of these tumors show characteristic BRAF-V600E mutation. However, unlike conventional GBMs, e-gbm lack specific diagnostic and prognostic markers. Hence, we aimed to molecularly characterize these tumors. An extensive review of literature was performed.In a multi-institutional effort, all the cases of glioblastoma of year 2017 were reviewed. Cases with predominant epithelioid morphology were analysed. Seven cases of e-gbm (adults:4 and pediatric: 3) were identified. Duration of symptoms varied from 2 weeks to one month. Radiologically, all cases were supratentorial, contrast enhancing with solid and cystic appearance. Majority of the cases were immunopositive for GFAP (71%), EMA (71%), S100 (71%) and vimentin (85%). All the cases showed ATRX, INI-1 and H3K27me3 expression. BRAFV600Emutation was seen in 28% of cases. TERT mutation was seen in 40% cases, while one case showed EGFR amplification. H3F3A mutations and PTEN deletions were seen in none. Although e-gbms are rare, epithelioid morphology of a CNS tumor in a young adult or children with areas of necrosis needs thorough histomorphological and genetic workup.