<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Baptista MJ</submitter><funding>"la Caixa" Foundation</funding><funding>Instituto de Salud Carlos III</funding><funding>“la Caixa” Foundation</funding><funding>Gilead Sciences S.L. Spain</funding><funding>Fundación Josep Carreras Contra la Leucemia</funding><funding>Agència de Gestió d'Ajuts Universitaris i de Recerca. Generalitat de Catalunya</funding><pagination>826-840</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC9828544</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>81(6)</volume><pubmed_abstract>The frequency of aggressive subtypes of B-cell non-Hodgkin lymphoma (B-NHL), such as high-grade B-cell lymphomas (HGBL) with MYC and BCL2 and/or BCL6 rearrangement (HGBL-DH/TH) or Burkitt-like lymphoma (BL) with 11q aberration, is not well known in the HIV setting. We aimed to characterise HIV-associated aggressive B-NHL according to the 2017 WHO criteria, and to identify genotypic and phenotypic features with prognostic impact. Seventy-five HIV-associated aggressive B-NHL were studied by immunohistochemistry (CD10, BCL2, BCL6, MUM1, MYC, and CD30), EBV-encoded RNAs (EBERs), and fluorescence in situ hybridisation (FISH) to evaluate the status of the MYC, BCL2, and BCL6 genes and chromosome 11q. The 2017 WHO classification criteria and the Hans algorithm, for the cell-of-origin classificati</pubmed_abstract><journal>Histopathology</journal><pubmed_title>Genetic and phenotypic characterisation of HIV-associated aggressive B-cell non-Hodgkin lymphomas, which do not occur specifically in this population: diagnostic and prognostic implications.</pubmed_title><pmcid>PMC9828544</pmcid><funding_grant_id>2017 SGR288</funding_grant_id><funding_grant_id>PI19/01588</funding_grant_id><funding_grant_id>GLD19/00121</funding_grant_id><pubmed_authors>Colomo L</pubmed_authors><pubmed_authors>Muncunill J</pubmed_authors><pubmed_authors>Gribben JG</pubmed_authors><pubmed_authors>Moraleda JM</pubmed_authors><pubmed_authors>Ferrandez A</pubmed_authors><pubmed_authors>Mate JL</pubmed_authors><pubmed_authors>Ribera JM</pubmed_authors><pubmed_authors>Abella E</pubmed_authors><pubmed_authors>Navarro JT</pubmed_authors><pubmed_authors>Aldamiz T</pubmed_authors><pubmed_authors>Terol MJ</pubmed_authors><pubmed_authors>Menarguez J</pubmed_authors><pubmed_authors>Garcia-Caro M</pubmed_authors><pubmed_authors>Calaminici M</pubmed_authors><pubmed_authors>Munoz-Marmol AM</pubmed_authors><pubmed_authors>Provencio M</pubmed_authors><pubmed_authors>Garcia-Ballesteros C</pubmed_authors><pubmed_authors>Alcoceba M</pubmed_authors><pubmed_authors>Climent F</pubmed_authors><pubmed_authors>Muntanola A</pubmed_authors><pubmed_authors>Abrisqueta P</pubmed_authors><pubmed_authors>Martinez-Trillos A</pubmed_authors><pubmed_authors>Tapia G</pubmed_authors><pubmed_authors>Garcia O</pubmed_authors><pubmed_authors>Briones J</pubmed_authors><pubmed_authors>Sancho JM</pubmed_authors><pubmed_authors>Martinez A</pubmed_authors><pubmed_authors>Baptista MJ</pubmed_authors><pubmed_authors>Montoto S</pubmed_authors><pubmed_authors>Veloza L</pubmed_authors><pubmed_authors>Gonzalez-Barca E</pubmed_authors></additional><is_claimable>false</is_claimable><name>Genetic and phenotypic characterisation of HIV-associated aggressive B-cell non-Hodgkin lymphomas, which do not occur specifically in this population: diagnostic and prognostic implications.</name><description>The frequency of aggressive subtypes of B-cell non-Hodgkin lymphoma (B-NHL), such as high-grade B-cell lymphomas (HGBL) with MYC and BCL2 and/or BCL6 rearrangement (HGBL-DH/TH) or Burkitt-like lymphoma (BL) with 11q aberration, is not well known in the HIV setting. We aimed to characterise HIV-associated aggressive B-NHL according to the 2017 WHO criteria, and to identify genotypic and phenotypic features with prognostic impact. Seventy-five HIV-associated aggressive B-NHL were studied by immunohistochemistry (CD10, BCL2, BCL6, MUM1, MYC, and CD30), EBV-encoded RNAs (EBERs), and fluorescence in situ hybridisation (FISH) to evaluate the status of the MYC, BCL2, and BCL6 genes and chromosome 11q. The 2017 WHO classification criteria and the Hans algorithm, for the cell-of-origin classificati</description><dates><release>2022-01-01T00:00:00Z</release><publication>2022 Dec</publication><modification>2025-04-21T18:01:04.925Z</modification><creation>2025-04-05T17:02:57.39Z</creation></dates><accession>S-EPMC9828544</accession><cross_references><pubmed>36109172</pubmed><doi>10.1111/his.14798</doi></cross_references></HashMap>