2020
DOI: 10.1007/s11910-020-01084-w
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A Practical Overview on the Molecular Biology of Meningioma

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Cited by 24 publications
(31 citation statements)
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“…The importance of pial blood supply in the development of peritumoral edema in meningiomas is well described. Of note, Delgado-Lopez et al [ 47 ] recently reviewed causes for peritumoral edema, and according to their observations, the most important cause for edema seems to be the tumor size, which usually reaches a larger volume in this area compared to other locations, which is probably due to the late perception of cognitive symptoms. Furthermore, higher tumor grade and absence of a clear demarcation between the lesion and healthy parenchyma (which was particularly high in this cohort with 35%) also seemed to be associated with edema.…”
Section: Discussionmentioning
confidence: 99%
“…The importance of pial blood supply in the development of peritumoral edema in meningiomas is well described. Of note, Delgado-Lopez et al [ 47 ] recently reviewed causes for peritumoral edema, and according to their observations, the most important cause for edema seems to be the tumor size, which usually reaches a larger volume in this area compared to other locations, which is probably due to the late perception of cognitive symptoms. Furthermore, higher tumor grade and absence of a clear demarcation between the lesion and healthy parenchyma (which was particularly high in this cohort with 35%) also seemed to be associated with edema.…”
Section: Discussionmentioning
confidence: 99%
“…POLR2A, PIK3CA, SMO, TERT, and SMARCE1 among others, or even combinations of them. 24 Some studies have shown that specific gene mutations seem to be predisposed to certain tumor subtypes and locations. 25 NF2 mutant meningiomas generally occur in lateral and posterior skull base or parasagittal sinus, falcate, annular and intraventricular meningiomas.…”
Section: Discussionmentioning
confidence: 99%
“…Next-generation sequencing revealed recurrent somatic mutations in the neurofibromin 2 (NF2), TNF receptor associated factor 7 (TRAF7), Krüppel-like factor 4 (KLF4), AKT serine/threonine kinase 1 (AKT1), smoothened (SMO), and phosphatidylinositol-4,5bisphosphate 3-kinase catalytic subunit alpha (PIK3CA) genes, which are collectively found in around 80% of sporadic MGMs and are associated with tumor location, histologic subtype, and clinical outcome [5,6,9,[15][16][17]. The most common chromosomal abnormality in MGM is found in chromosome 22 and occurs 40-70% of grade I tumors.…”
Section: Molecular Changes and Novel Molecularly-targeted Therapeutic Strategiesmentioning
confidence: 99%
“…In addition to histopathological analysis, positron emission tomography (PET) imaging has contributed with the distinction between low-and high-grade MGMs [4]. Also, other classification methods have been more recently proposed, based on molecular markers such as DNA methylation profiles [5,6].…”
Section: Introductionmentioning
confidence: 99%