| Literature DB >> 30238518 |
Sun Ah Shin1, Bokyung Ahn2, Seung-Ki Kim3, Hyoung Jin Kang4, Sumihito Nobusawa5, Takashi Komori6, Sung-Hye Park1.
Abstract
Astroblastoma is a rare glial neoplasm that occurs mostly in the cerebral hemisphere of children, adolescents and young adults. Although astroblastic perivascular pseudorosettes are unique histopathology of this neoplasm, diagnosis is usually challenging. Recently, it was discovered that the meningioma 1 gene (MN1)-altered pediatric central nervous system high-grade neuroepithelial tumors are actually astroblastomas. This case report presents a rare brainstem astroblastoma, with an unusual immunoprofile: negative for glial fibrillary acidic protein and oligodendrocyte transcription factor 2, but with a robust expression of pancytokeratin and epithelial membrane antigen. The diagnosis was confirmed based on the detection of MN1 rearrangement in a fluorescence in situ hybridization study, in addition to typical histopathology. Here we discuss the diagnostic pitfalls and unclear grading system along with a literature review.Entities:
Keywords: zzm321990MN1; astroblastoma; gene rearrangement; glioma; ultrastructure
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Year: 2018 PMID: 30238518 DOI: 10.1111/neup.12514
Source DB: PubMed Journal: Neuropathology ISSN: 0919-6544 Impact factor: 1.906