Meningiomas: A review of general, histopathological, clinical and molecular characteristics.
Animals
Biomarkers, Tumor
/ genetics
Chromosome Deletion
Chromosomes, Human, Pair 22
Gene Expression Regulation, Neoplastic
Genetic Predisposition to Disease
Humans
Meningeal Neoplasms
/ genetics
Meningioma
/ genetics
Mutation
Neurofibromin 2
/ genetics
Phenotype
Prognosis
Signal Transduction
Telomerase
/ genetics
Brain invasion
Histopathology
Meningiomas
Molecular
Necrosis
Resection
Journal
Pathology, research and practice
ISSN: 1618-0631
Titre abrégé: Pathol Res Pract
Pays: Germany
ID NLM: 7806109
Informations de publication
Date de publication:
Jul 2021
Jul 2021
Historique:
received:
22
03
2021
revised:
04
05
2021
accepted:
07
05
2021
pubmed:
16
5
2021
medline:
15
12
2021
entrez:
15
5
2021
Statut:
ppublish
Résumé
In this review, the main histological and molecular characteristics of meningiomas will be addressed, as well as the aspects most related to clinical conditions, treatment, and survival of patients, enabling a better understanding of these tumors behavior. This study was conducted with the search for published studies available on NCBI, PubMed, MEDLINE, Scielo and Google Scholar. Relevant documents have been identified and 50 articles were selected. The main points about meningiomas were characterized, as well as the histological presence of spontaneous necrosis in grade I and brain invasion as diagnostic criteria, their molecular origin related to deletion of chromosome 22 and mutations in theNF2 and TERT genes, in addition to their clinical characteristics. The preferential treatment remains the total resection of the tumor. The information about meningiomas is well known and necessary, but it is expected that more work will emerge related to the behavior of these tumors, and that the scientific community will obtain more clarity about the best ways to conduct the patients treatment.
Identifiants
pubmed: 33991850
pii: S0344-0338(21)00137-0
doi: 10.1016/j.prp.2021.153476
pii:
doi:
Substances chimiques
Biomarkers, Tumor
0
NF2 protein, human
0
Neurofibromin 2
0
TERT protein, human
EC 2.7.7.49
Telomerase
EC 2.7.7.49
Types de publication
Journal Article
Review
Langues
eng
Sous-ensembles de citation
IM
Pagination
153476Informations de copyright
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