<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>11(1)</volume><submitter>Beddok A</submitter><funding>Department of Clinical Research, Amiens University Hospital, France</funding><pubmed_abstract>Soft tissue sarcoma represents about 1% of all adult cancers. Occurrence of multiple sarcomas in a same individual cannot be fortuitous. A 72-year-old patient had between 2007 and 2016 a glomangiopericytal tumor of the right forearm and a succession of sarcomas of the extremities: a leiomyosarcoma of the left buttock, a myxofibrosarcoma (MFS) of the right forearm, a MFS of the left scapula, a left latero-thoracic MFS and two undifferentiated sarcomas on the left forearm. Pathological examination of the six locations was not in favor of disease with local/distant recurrences but could not confirm different diseases. An extensive molecular analysis including DNA-array, RNA-sequencing and DNA-Sanger-sequencing, was thus performed to determine the link between them. The genomic profile of the </pubmed_abstract><journal>Scientific reports</journal><pagination>9765</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC8105326</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Germinal GLT8D1, GATAD2A and SLC25A39 mutations in a patient with a glomangiopericytal tumor and five different sarcomas over a 10-year period.</pubmed_title><pmcid>PMC8105326</pmcid><pubmed_authors>Thebault N</pubmed_authors><pubmed_authors>Chauffert B</pubmed_authors><pubmed_authors>Sevestre H</pubmed_authors><pubmed_authors>Beddok A</pubmed_authors><pubmed_authors>Le Guellec S</pubmed_authors><pubmed_authors>Perot G</pubmed_authors><pubmed_authors>Coutte A</pubmed_authors><pubmed_authors>Chibon F</pubmed_authors></additional><is_claimable>false</is_claimable><name>Germinal GLT8D1, GATAD2A and SLC25A39 mutations in a patient with a glomangiopericytal tumor and five different sarcomas over a 10-year period.</name><description>Soft tissue sarcoma represents about 1% of all adult cancers. Occurrence of multiple sarcomas in a same individual cannot be fortuitous. A 72-year-old patient had between 2007 and 2016 a glomangiopericytal tumor of the right forearm and a succession of sarcomas of the extremities: a leiomyosarcoma of the left buttock, a myxofibrosarcoma (MFS) of the right forearm, a MFS of the left scapula, a left latero-thoracic MFS and two undifferentiated sarcomas on the left forearm. Pathological examination of the six locations was not in favor of disease with local/distant recurrences but could not confirm different diseases. An extensive molecular analysis including DNA-array, RNA-sequencing and DNA-Sanger-sequencing, was thus performed to determine the link between them. The genomic profile of the </description><dates><release>2021-01-01T00:00:00Z</release><publication>2021 May</publication><modification>2026-04-18T05:30:06.828Z</modification><creation>2022-02-10T09:51:23.753Z</creation></dates><accession>S-EPMC8105326</accession><cross_references><pubmed>33963205</pubmed><doi>10.1038/s41598-021-88671-0</doi></cross_references></HashMap>