PTCH1 mutant small cell glioblastoma in a patient with Gorlin syndrome: A case report
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DOI: 10.3892/ol.2022.13446
Abstract: Gorlin syndrome or nevoid basal cell carcinoma syndrome is a rare genetic disease characterized by predisposition to congenital defects, basal cell carcinomas and medulloblastoma. The syndrome results from a heritable mutation in PATCHED1 (PTCH1), causing… read more here.
Keywords: cell; cell glioblastoma; patient gorlin; small cell ... See more keywords
Glioblastoma: Changing concepts in the WHO CNS5 classification
Sign Up to like & getrecommendations! Published in 2022 at "Indian Journal of Pathology and Microbiology"
DOI: 10.4103/ijpm.ijpm_1109_21
Abstract: Glioblastoma is the most common malignant central nervous system (CNS) tumor in adults. Acute common clinical symptoms include headache, seizure, behavior changes, focal neurological deficits, and signs of increased intracranial pressure. The classic MRI finding… read more here.
Keywords: glioblastoma changing; glioblastoma; cell glioblastoma; classification ... See more keywords