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Identification of a Novel BRCA1 Alteration in Recurrent Melanocytoma Resulting in Increased Proliferation.
- Source :
-
Journal of neuropathology and experimental neurology [J Neuropathol Exp Neurol] 2020 Nov 01; Vol. 79 (11), pp. 1233-1238. - Publication Year :
- 2020
-
Abstract
- Primary meningeal melanocytomas are rare tumors of the central nervous system. Although they are considered benign neoplasms, some reports describe recurrent rates up to 45%. Little is known about their genetic and epigenetic landscape because of their infrequency. Even less has been described about markers with prognostic value. Here we describe a patient who developed a primary meningeal melanocytoma, suffered 3 recurrences in a period of 6 years and died of the tumor. The genetic and epigenetic changes explored confirmed GNAQ mutation as an initiating event. We found an epigenetic alteration of GSTP1, a feature that has recently been described in meningiomas, from the beginning of the disease. In addition, there was loss of heterozygosity in BRCA1 beginning in the second recurrence that was linked to an increase in the proliferation index; this suggested a progression pathway similar to the one described in uveal melanomas. These findings underscore the necessity of further research focused on these tumors.<br /> (© 2020 American Association of Neuropathologists, Inc. All rights reserved.)
- Subjects :
- Cell Proliferation genetics
Fatal Outcome
Female
GTP-Binding Protein alpha Subunits, Gq-G11 genetics
Glutathione S-Transferase pi genetics
Humans
Middle Aged
Mutation
Neoplasm Recurrence, Local pathology
BRCA1 Protein genetics
Melanoma genetics
Melanoma pathology
Meningeal Neoplasms genetics
Meningeal Neoplasms pathology
Neoplasm Recurrence, Local genetics
Subjects
Details
- Language :
- English
- ISSN :
- 1554-6578
- Volume :
- 79
- Issue :
- 11
- Database :
- MEDLINE
- Journal :
- Journal of neuropathology and experimental neurology
- Publication Type :
- Academic Journal
- Accession number :
- 32974655
- Full Text :
- https://doi.org/10.1093/jnen/nlaa089