Lymphoplasmacytic lymphoma associated with diffuse large B-cell lymphoma: Progression or divergent evolution?

Lymphoplasmacytic lymphoma (LPL) is an indolent mature B-cell-neoplasm with involvement of the bone marrow. At least 90% of LPLs carry MYD88-L265P mutation and some of them (~10%) transform into diffuse large B-cell-lymphoma (DLBCL). Over the past 15 years we have collected 7 cases where the both LP...

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Veröffentlicht in:PloS one 2020-11, Vol.15 (11), p.e0241634-e0241634
Hauptverfasser: Boiza-Sánchez, Macarena, Manso, Rebeca, Balagué, Olga, Chamizo, Cristina, Askari, Elham, Salgado, Rocío Nieves, Blas-López, Carlos, Aguirregoicoa-García, Elena, Menárguez, Javier, Santonja, Carlos, Adrados, Magdalena, Limeres-González, Miguel Ángel, Piris, Miguel Ángel, Rodríguez-Pinilla, Socorro María
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Sprache:eng
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Zusammenfassung:Lymphoplasmacytic lymphoma (LPL) is an indolent mature B-cell-neoplasm with involvement of the bone marrow. At least 90% of LPLs carry MYD88-L265P mutation and some of them (~10%) transform into diffuse large B-cell-lymphoma (DLBCL). Over the past 15 years we have collected 7 cases where the both LPL and DLBCL were diagnosed in the same patient. Clinical records, analytical data and histopathological specimens were reviewed. FISH studies on paraffin-embedded tissue for MYC, BCL2 and BCL6 genes were performed, as well as MYD88-L265P mutation and IGH rearrangement analysis by PCR. A mutational study was done by massive next generation sequencing (NGS). There were 4 women and 3 men between 36-91 years of age. Diagnoses were made simultaneously in 4 patients. In two cases the LPL appeared before the DLBCL and in the remaining case the high-grade component was discovered 5 years before the LPL. In 6 cases both samples shared the MYD88-L265P mutation. IGH rearrangement analysis showed overlapping features in two of 6 cases tested. Mutational study was evaluable in three cases for both samples showing shared and divergent mutations. These data suggest different mechanisms of DLBCL development in LPL patients.
ISSN:1932-6203
1932-6203
DOI:10.1371/journal.pone.0241634