<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Leung E</submitter><funding>NCI NIH HHS</funding><pagination>4467-4476</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC12376075</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>103(11)</volume><pubmed_abstract>Recent advances in Rosai-Dorfman-Destombes disease (RDD), notably molecular testing, targeted therapy, and PET-CT imaging, hold promise for better recognition and improved outcomes. This study presents patients diagnosed and treated in a "real world" setting, where navigating limited resources must be considered. This retrospective single-center review includes 15 adult patients diagnosed with RDD at Vancouver General Hospital between November 2015 and October 2023. The cohort comprised five males and ten females with a median age 53 years (range 19-80 years). All 15 patients had extra-nodal disease; 11 patients exclusively had extra-nodal disease, and four patients also had lymph node involvement. Seven patients had tissue next-generation sequencing, identifying MAP2K1 mutations in four cases and a KRAS p.K117N mutation in one case that was treated with targeted therapy using trametinib. PET-CT was used for disease staging in four cases. Six patients with refractory disease tolerated lenalidomide and dexamethasone without significant toxicity; three patients achieved complete response, and three had partial response. This study highlights RDD's diverse extra-nodal manifestations. Lenalidomide combined with dexamethasone is an effective and well-tolerated treatment option for select patients, especially those with refractory disease. Broad utilization of NGS and PET-CT can positively influence management decisions.</pubmed_abstract><journal>Annals of hematology</journal><pubmed_title>Rosai-Dorfman-Destombes disease in adults: a single center experience.</pubmed_title><pmcid>PMC12376075</pmcid><funding_grant_id>P30 CA008748</funding_grant_id><funding_grant_id>R37 CA259260</funding_grant_id><pubmed_authors>Diamond EL</pubmed_authors><pubmed_authors>You XJ</pubmed_authors><pubmed_authors>Harrison R</pubmed_authors><pubmed_authors>Carruthers M</pubmed_authors><pubmed_authors>Skinnider BF</pubmed_authors><pubmed_authors>Varghese J</pubmed_authors><pubmed_authors>Ng T</pubmed_authors><pubmed_authors>Peterson E</pubmed_authors><pubmed_authors>Chen LYC</pubmed_authors><pubmed_authors>Slack GW</pubmed_authors><pubmed_authors>Leung E</pubmed_authors><pubmed_authors>Dutz J</pubmed_authors><pubmed_authors>Young S</pubmed_authors><pubmed_authors>Tsang PWK</pubmed_authors><pubmed_authors>Stubbins R</pubmed_authors><pubmed_authors>Lim H</pubmed_authors><pubmed_authors>Pryma C</pubmed_authors><pubmed_authors>Burrell S</pubmed_authors><pubmed_authors>Murphy S</pubmed_authors></additional><is_claimable>false</is_claimable><name>Rosai-Dorfman-Destombes disease in adults: a single center experience.</name><description>Recent advances in Rosai-Dorfman-Destombes disease (RDD), notably molecular testing, targeted therapy, and PET-CT imaging, hold promise for better recognition and improved outcomes. This study presents patients diagnosed and treated in a "real world" setting, where navigating limited resources must be considered. This retrospective single-center review includes 15 adult patients diagnosed with RDD at Vancouver General Hospital between November 2015 and October 2023. The cohort comprised five males and ten females with a median age 53 years (range 19-80 years). All 15 patients had extra-nodal disease; 11 patients exclusively had extra-nodal disease, and four patients also had lymph node involvement. Seven patients had tissue next-generation sequencing, identifying MAP2K1 mutations in four cases and a KRAS p.K117N mutation in one case that was treated with targeted therapy using trametinib. PET-CT was used for disease staging in four cases. Six patients with refractory disease tolerated lenalidomide and dexamethasone without significant toxicity; three patients achieved complete response, and three had partial response. This study highlights RDD's diverse extra-nodal manifestations. Lenalidomide combined with dexamethasone is an effective and well-tolerated treatment option for select patients, especially those with refractory disease. Broad utilization of NGS and PET-CT can positively influence management decisions.</description><dates><release>2024-01-01T00:00:00Z</release><publication>2024 Nov</publication><modification>2026-05-08T06:46:39.917Z</modification><creation>2026-04-07T23:30:31.181Z</creation></dates><accession>S-EPMC12376075</accession><cross_references><pubmed>39331156</pubmed><doi>10.1007/s00277-024-06019-w</doi></cross_references></HashMap>