<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Sahm K</submitter><funding>Deutsche Forschungsgemeinschaft</funding><funding>Gemeinnützige Hertie-Stiftung</funding><funding>Else Kröner-Fresenius-Stiftung (Else Kroner-Fresenius Foundation)</funding><funding>Deutsche Forschungsgemeinschaft (German Research Foundation)</funding><funding>Gemeinnützige Hertie-Stiftung (Hertie Foundation)</funding><funding>Else Kröner-Fresenius-Stiftung</funding><pagination>186</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC10728097</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>3(1)</volume><pubmed_abstract>&lt;h4>Background&lt;/h4>Concurrent malignant brain tumors in patients with multiple sclerosis (MS) constitute a rare but paradigmatic phenomenon for studying neuroimmunological mechanisms from both molecular and clinical perspectives.&lt;h4>Methods&lt;/h4>A multicenter cohort of 26 patients diagnosed with both primary brain tumors and multiple sclerosis was studied for disease localization, tumor treatment-related MS activity, and molecular characteristics specific for diffuse glioma in MS patients.&lt;h4>Results&lt;/h4>MS neither predisposes nor protects from the development of gliomas. Patients with glioblastoma WHO grade 4 without isocitratdehydrogenase (IDH) mutations have a longstanding history of MS, whereas patients diagnosed with IDH-mutant astrocytoma WHO grade 2 receive multiple sclerosis diagnos</pubmed_abstract><journal>Communications medicine</journal><pubmed_title>Concurrent gliomas in patients with multiple sclerosis.</pubmed_title><pmcid>PMC10728097</pmcid><funding_grant_id>2019_EKMS.23</funding_grant_id><funding_grant_id>39404578</funding_grant_id><funding_grant_id>P1200013</funding_grant_id><pubmed_authors>Eisele P</pubmed_authors><pubmed_authors>Bendszus M</pubmed_authors><pubmed_authors>Mildenberger I</pubmed_authors><pubmed_authors>Herold-Mende C</pubmed_authors><pubmed_authors>von Deimling A</pubmed_authors><pubmed_authors>Seliger C</pubmed_authors><pubmed_authors>Konig L</pubmed_authors><pubmed_authors>Zeiner PS</pubmed_authors><pubmed_authors>Meuth SG</pubmed_authors><pubmed_authors>Capper D</pubmed_authors><pubmed_authors>Sperk E</pubmed_authors><pubmed_authors>Schrimpf D</pubmed_authors><pubmed_authors>Sahm F</pubmed_authors><pubmed_authors>Sahm K</pubmed_authors><pubmed_authors>Tabatabai G</pubmed_authors><pubmed_authors>Platten M</pubmed_authors><pubmed_authors>Wick W</pubmed_authors><pubmed_authors>Breckwoldt MO</pubmed_authors><pubmed_authors>Ratliff M</pubmed_authors><pubmed_authors>Kessler T</pubmed_authors></additional><is_claimable>false</is_claimable><name>Concurrent gliomas in patients with multiple sclerosis.</name><description>&lt;h4>Background&lt;/h4>Concurrent malignant brain tumors in patients with multiple sclerosis (MS) constitute a rare but paradigmatic phenomenon for studying neuroimmunological mechanisms from both molecular and clinical perspectives.&lt;h4>Methods&lt;/h4>A multicenter cohort of 26 patients diagnosed with both primary brain tumors and multiple sclerosis was studied for disease localization, tumor treatment-related MS activity, and molecular characteristics specific for diffuse glioma in MS patients.&lt;h4>Results&lt;/h4>MS neither predisposes nor protects from the development of gliomas. Patients with glioblastoma WHO grade 4 without isocitratdehydrogenase (IDH) mutations have a longstanding history of MS, whereas patients diagnosed with IDH-mutant astrocytoma WHO grade 2 receive multiple sclerosis diagnos</description><dates><release>2023-01-01T00:00:00Z</release><publication>2023 Dec</publication><modification>2026-07-14T22:42:51.951Z</modification><creation>2026-06-26T03:07:05.686Z</creation></dates><accession>S-EPMC10728097</accession><cross_references><pubmed>38110626</pubmed><doi>10.1038/s43856-023-00381-y</doi></cross_references></HashMap>