<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>102(10)</volume><submitter>Jallades L</submitter><pubmed_abstract>Splenic diffuse red pulp lymphoma is an indolent small B-cell lymphoma recognized as a provisional entity in the World Health Organization 2008 classification. Its precise relationship to other related splenic B-cell lymphomas with frequent leukemic involvement or other lymphoproliferative disorders remains undetermined. We performed whole-exome sequencing to explore the genetic landscape of ten cases of splenic diffuse red pulp lymphoma using paired tumor and normal samples. A selection of 109 somatic mutations was then evaluated in a cohort including 42 samples of splenic diffuse red pulp lymphoma and compared to those identified in 46 samples of splenic marginal zone lymphoma and eight samples of hairy-cell leukemia. Recurrent mutations or losses in &lt;i>BCOR&lt;/i> (the gene encoding the BC</pubmed_abstract><journal>Haematologica</journal><pagination>1758-1766</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC5622860</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Exome sequencing identifies recurrent &lt;i>BCOR&lt;/i> alterations and the absence of &lt;i>KLF2&lt;/i>, &lt;i>TNFAIP3&lt;/i> and &lt;i>MYD88&lt;/i> mutations in splenic diffuse red pulp small B-cell lymphoma.</pubmed_title><pmcid>PMC5622860</pmcid><pubmed_authors>Verney A</pubmed_authors><pubmed_authors>Desvignes JP</pubmed_authors><pubmed_authors>Hayette S</pubmed_authors><pubmed_authors>Magaud JP</pubmed_authors><pubmed_authors>Salles G</pubmed_authors><pubmed_authors>Jallades L</pubmed_authors><pubmed_authors>Salgado D</pubmed_authors><pubmed_authors>Beroud C</pubmed_authors><pubmed_authors>Berger F</pubmed_authors><pubmed_authors>Huet S</pubmed_authors><pubmed_authors>Callet-Bauchu E</pubmed_authors><pubmed_authors>Genestier L</pubmed_authors><pubmed_authors>Chabane K</pubmed_authors><pubmed_authors>Baseggio L</pubmed_authors><pubmed_authors>Sujobert P</pubmed_authors><pubmed_authors>Traverse-Glehen A</pubmed_authors><pubmed_authors>Levy N</pubmed_authors><pubmed_authors>Felman P</pubmed_authors></additional><is_claimable>false</is_claimable><name>Exome sequencing identifies recurrent &lt;i>BCOR&lt;/i> alterations and the absence of &lt;i>KLF2&lt;/i>, &lt;i>TNFAIP3&lt;/i> and &lt;i>MYD88&lt;/i> mutations in splenic diffuse red pulp small B-cell lymphoma.</name><description>Splenic diffuse red pulp lymphoma is an indolent small B-cell lymphoma recognized as a provisional entity in the World Health Organization 2008 classification. Its precise relationship to other related splenic B-cell lymphomas with frequent leukemic involvement or other lymphoproliferative disorders remains undetermined. We performed whole-exome sequencing to explore the genetic landscape of ten cases of splenic diffuse red pulp lymphoma using paired tumor and normal samples. A selection of 109 somatic mutations was then evaluated in a cohort including 42 samples of splenic diffuse red pulp lymphoma and compared to those identified in 46 samples of splenic marginal zone lymphoma and eight samples of hairy-cell leukemia. Recurrent mutations or losses in &lt;i>BCOR&lt;/i> (the gene encoding the BC</description><dates><release>2017-01-01T00:00:00Z</release><publication>2017 Oct</publication><modification>2026-05-06T04:10:05.39Z</modification><creation>2019-07-24T07:12:28Z</creation></dates><accession>S-EPMC5622860</accession><cross_references><pubmed>28751561</pubmed><doi>10.3324/haematol.2016.160192</doi></cross_references></HashMap>