<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Saoud C</submitter><funding>NCI NIH HHS</funding><pagination>1302-1317</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC12150273</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>48(10)</volume><pubmed_abstract>GLI1 -altered mesenchymal tumor is a recently described distinct pathologic entity with an established risk of malignancy, being defined molecularly by either GLI1 gene fusions or amplifications. The clinicopathologic overlap of tumors driven by the 2 seemingly distinct mechanisms of GLI1 activation is still emerging. Herein, we report the largest series of molecularly confirmed GLI1 -altered mesenchymal neoplasms to date, including 23 GLI1- amplified and 15 GLI1 -rearranged new cases, and perform a comparative clinicopathologic, genomic, and survival investigation. GLI1- rearranged tumors occurred in younger patients (42 vs. 52 y) and were larger compared with GLI1 -amplified tumors (5.6 cm vs. 1.5 cm, respectively). Histologic features were overall similar between the 2 groups, showing a</pubmed_abstract><journal>The American journal of surgical pathology</journal><pubmed_title>A Comprehensive Clinicopathologic and Molecular Reappraisal of GLI1 -altered Mesenchymal Tumors with Pooled Outcome Analysis Showing Poor Survival in GLI1 - amplified Versus GLI1- rearranged Tumors.</pubmed_title><pmcid>PMC12150273</pmcid><funding_grant_id>P30 CA008748</funding_grant_id><funding_grant_id>P50 CA217694</funding_grant_id><pubmed_authors>Albritton K</pubmed_authors><pubmed_authors>Michal M</pubmed_authors><pubmed_authors>Antonescu CR</pubmed_authors><pubmed_authors>Dermawan JK</pubmed_authors><pubmed_authors>Dashti N</pubmed_authors><pubmed_authors>Saoud C</pubmed_authors><pubmed_authors>Dickson BC</pubmed_authors><pubmed_authors>Agaimy A</pubmed_authors><pubmed_authors>Chen JF</pubmed_authors><pubmed_authors>Kosemehmetoglu K</pubmed_authors><pubmed_authors>Agaram NP</pubmed_authors><pubmed_authors>Rosenblum MK</pubmed_authors><pubmed_authors>Din NU</pubmed_authors></additional><is_claimable>false</is_claimable><name>A Comprehensive Clinicopathologic and Molecular Reappraisal of GLI1 -altered Mesenchymal Tumors with Pooled Outcome Analysis Showing Poor Survival in GLI1 - amplified Versus GLI1- rearranged Tumors.</name><description>GLI1 -altered mesenchymal tumor is a recently described distinct pathologic entity with an established risk of malignancy, being defined molecularly by either GLI1 gene fusions or amplifications. The clinicopathologic overlap of tumors driven by the 2 seemingly distinct mechanisms of GLI1 activation is still emerging. Herein, we report the largest series of molecularly confirmed GLI1 -altered mesenchymal neoplasms to date, including 23 GLI1- amplified and 15 GLI1 -rearranged new cases, and perform a comparative clinicopathologic, genomic, and survival investigation. GLI1- rearranged tumors occurred in younger patients (42 vs. 52 y) and were larger compared with GLI1 -amplified tumors (5.6 cm vs. 1.5 cm, respectively). Histologic features were overall similar between the 2 groups, showing a</description><dates><release>2024-01-01T00:00:00Z</release><publication>2024 Oct</publication><modification>2026-06-03T23:34:58.726Z</modification><creation>2026-05-03T03:11:52.811Z</creation></dates><accession>S-EPMC12150273</accession><cross_references><pubmed>38934567</pubmed><doi>10.1097/pas.0000000000002272</doi><doi>10.1097/PAS.0000000000002272</doi></cross_references></HashMap>