Divergence in intra-tumor variant frequencies in sporadic vestibular schwannomas as a potential indication for mosaic NF2-related schwannomatosis?

Vestibular schwannomas (VSs) are benign tumors of the eighth cranial nerve and the hallmark of NF2-related schwannomatosis. However, the majority of these tumors occur sporadically, arising from two inactivating alterations of the NF2 gene. In this study, we re-evaluated a total of 29 VSs, each harboring two intragenic pathogenic NF2 variants. In the six NF2-associated VSs, the intra-tumor variant frequencies differed substantially. Three of these cases were mosaic, as the pathogenic NF2 variants were absent in the corresponding blood. By contrast, in the majority (20/23, 87%) of sporadic VSs, the allele frequencies of the two pathogenic NF2 variants were nearly identical. Nevertheless, in two sporadic VSs, the intra-tumor variant frequencies were clearly divergent, suggesting the presence of cells with only one variant—the one with the higher allele frequency. We hypothesize that divergence in intra-tumor variant frequencies may provide a potential genetic indication for mosaic NF2-related schwannomatosis, even in cases that appear sporadic.

Authors

Institutions

Publication Details

Journal
Neurogenetics
Published
2026-04-27
DOI
https://doi.org/10.1007/s10048-026-00903-5
Primary Topic
Neurofibromatosis and Schwannoma Cases
Type
article
Field-Weighted Citation Impact
0.00
Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

Divergence in intra-tumor variant frequencies in sporadic vestibular schwannomas as a potential indication for mosaic NF2-related schwannomatosis?

Lan Kluwe, Said Farschtschi, Tabea Hartung, Steffen Rosahl
Neurogenetics
Neurofibromatosis and Schwannoma Cases
article

Divergence in intra-tumor variant frequencies in sporadic vestibular schwannomas as a potential indication for mosaic NF2-related schwannomatosis?

Lan Kluwe, Said Farschtschi, Tabea Hartung, Steffen Rosahl
article en

Abstract

Vestibular schwannomas (VSs) are benign tumors of the eighth cranial nerve and the hallmark of NF2-related schwannomatosis. However, the majority of these tumors occur sporadically, arising from two inactivating alterations of the NF2 gene. In this study, we re-evaluated a total of 29 VSs, each harboring two intragenic pathogenic NF2 variants. In the six NF2-associated VSs, the intra-tumor variant frequencies differed substantially. Three of these cases were mosaic, as the pathogenic NF2 variants were absent in the corresponding blood. By contrast, in the majority (20/23, 87%) of sporadic VSs, the allele frequencies of the two pathogenic NF2 variants were nearly identical. Nevertheless, in two sporadic VSs, the intra-tumor variant frequencies were clearly divergent, suggesting the presence of cells with only one variant—the one with the higher allele frequency. We hypothesize that divergence in intra-tumor variant frequencies may provide a potential genetic indication for mosaic NF2-related schwannomatosis, even in cases that appear sporadic.

NeurogeneticsVol. 27(1)
Universität Hamburg (DE), University of Erfurt (DE), University Medical Center Hamburg-Eppendorf (DE)
Good health and well-being
Openalex Percentile: Top 9%
Neurofibromatosis and Schwannoma Cases
AI Navigator

Ask Laika to Summarize, Analyze, and Connect papers live on the map.

Summarize Papers & Methodologies

Extract key findings, datasets, and comparative methods across publications.

Benchmark Rankings & Visual Analytics

Rank top research institutions, authors, funders, topics, and journals by Field-Weighted Citation Impact (FWCI) and paper volume with instant charts.

Connect Distant Disciplines

Bridge topological clusters on the map to find hidden collaborative intersections.