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Palabras clave – provistas por la editorial

lymphomas in PLWH; KSHV/HHV8; EBV; lymphoma classification; management; cART; HLX; HOXB9; NFIB; PBX1; STAT3; TLX2; autoimmune hemolytic anemia; cold agglutinin; B-cell lymphoproliferative disorder; lymphomagenesis; methylation; histone modification; indolent; T-cell; NK-cell; lymphoproliferative disorder; gastrointestinal tract; genetics; cell of origin; T follicular helper cells; TFH lymphoma; angioimmunoblastic T-cell lymphoma; follicular T-cell lymphoma; peripheral T-cell lymphoma of T-follicular helper immunophenotype; peripheral T-cell lymphoma; primary cutaneous B-cell lymphoma; primary cutaneous marginal zone B-cell lymphoma; primary cutaneous follicle centre lymphoma; primary cutaneous diffuse large B-cell lymphoma, leg-type; primary cutaneous diffuse large B-cell lymphoma, not otherwise specified; intravascular B-cell lymphoma; EBV+ mucocutaneous ulcer; Burkitt lymphoma; epidemiology; Plasmodium falciparum; Epstein Barr virus; registry studies; multimodal cancer; non-Hodgkin lymphoma; HIV/AIDS; follicular lymphoma; in situ follicular neoplasia; FL transformation; FL in young patients; diffuse large B-cell lymphoma NOS; high grade B-cell lymphoma; lymphoma; gene expression profiling; tumor microenvironment; diagnostics; centrocytic lymphoma; intermediate lymphocytic lymphoma; Jaffe; mantle cell lymphoma; mantle zone lymphoma; cyclin D1; lymphomas; people living with HIV; tumor prevention in people living with HIV; KSHV; BCL2 rearrangement; genetic alterations; histological transformation; targeted therapies; transformed follicular lymphoma; lymphoproliferative neoplasms of uncertain biological significance; monoclonal B-cell lymphocytosis; “in situ” follicular neoplasia; “in situ” mantle cell neoplasia; atypical germinal centers; large B-cell lymphoma with IRF4 rearrangement; “in situ” high-grade B lymphomas; Hodgkin lymphoma