Please use this identifier to cite or link to this item:
https://hdl.handle.net/2445/199446
Title: | A unifying hypothesis for PNMZL and PTFL: morphological variants with a common molecular profile |
Author: | Salmerón Villalobos, Julia Egan, Caoimhe Borgmann, Vanessa Müller, Inga González Farré, Blanca Ramis Zaldívar, Joan Enric Nann, Dominik Balagué Ponz, Olga López Guerra, Mònica Colomer, Dolors Oschlies, Ilske Klapper, Wolfram Glaser, Selina Ko, Young Hyeh Bonzheim, Irina Siebert, Reiner Fend, Falko Pittaluga, Stefania Campo Güerri, Elias Salaverria Frigola, Itziar Jaffe, Elaine S. Quintanilla Martinez, Leticia |
Keywords: | B-cell lymphoma Mutations Cèl·lules B Limfomes Biologia molecular B cells Lymphomas Molecular biology |
Issue Date: | 24-May-2022 |
Publisher: | American Society of Hematology |
Abstract: | Pediatric nodal marginal zone lymphoma (PNMZL) is an uncommon B-cell neoplasm affecting mainly male children and young adults. This indolent lymphoma has distinct characteristics that differ from those of conventional nodal marginal zone lymphoma (NMZL). Clinically, it exhibits overlapping features with pediatric-type follicular lymphoma (PTFL). To explore the differences between PNMZL and adult NMZL and its relationship to PTFL, a series of 45 PNMZL cases were characterized morphologically and genetically by using an integrated approach; this approach included whole-exome sequencing in a subset of cases, targeted next-generation sequencing, and copy number and DNA methylation arrays. Fourteen cases (31%) were diagnosed as PNMZL, and 31 cases (69%) showed overlapping histologic features between PNMZL and PTFL, including a minor component of residual serpiginous germinal centers reminiscent of PTFL and a dominant interfollicular B-cell component characteristic of PNMZL. All cases displayed low genomic complexity (1.2 alterations per case) with recurrent 1p36/TNFRSF14 copy number-neutral loss of heterozygosity alterations and copy number loss (11%). Similar to PTFL, the most frequently mutated genes in PNMZL were MAP2K1 (42%), TNFRSF14 (36%), and IRF8 (34%). DNA methylation analysis revealed no major differences between PTFL and PNMZL. Genetic alterations typically seen in conventional NMZL were absent in PNMZL. In summary, overlapping clinical, morphologic, and molecular findings (including low genetic complexity; recurrent alterations in MAP2K1, TNFRSF14, and IRF8; and similar methylation profiles) indicate that PNMZL and PTFL are likely part of a single disease with variation in the histologic spectrum. The term "pediatric-type follicular lymphoma with and without marginal zone differentiation" is suggested.Licensed under Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International (CC BY-NC-ND 4.0), permitting only noncommercial, nonderivative use with attribution. All other rights reserved. |
Note: | Reproducció del document publicat a: https://doi.org/10.1182/bloodadvances.2022007322 |
It is part of: | Blood Advances, 2022, vol. 6, num. 16, p. 4661-4674 |
URI: | https://hdl.handle.net/2445/199446 |
Related resource: | https://doi.org/10.1182/bloodadvances.2022007322 |
ISSN: | 2473-9537 |
Appears in Collections: | Articles publicats en revistes (IDIBAPS: Institut d'investigacions Biomèdiques August Pi i Sunyer) |
Files in This Item:
File | Description | Size | Format | |
---|---|---|---|---|
A unifying hypothesis for PNMZL and PTFL_BloodAdvances.pdf | 3.84 MB | Adobe PDF | View/Open |
This item is licensed under a
Creative Commons License