Lymphoproliferation in inborn errors of immunity: From challenging diagnosis to histologic revision

Inborn errors of immunity (IEI) are genetic disorders that not only heighten infection risk but also disrupt immune regulation, frequently leading to lymphoid tissue overgrowth known as lymphoid proliferations (LPD). We retrospectively reviewed 38 patients with genetically or clinically confirmed IEI and persistent LPD, comparing those with nonneoplastic/reactive hyperplasia to those who developed overt lymphoid neoplasm (lymphoma). Overall, 26% developed lymphoma—predominantly classical Hodgkin lymphoma or diffuse large B cell lymphoma—often after earlier IEI onset. Immunophenotyping and principal component analysis revealed that patients with common variable immunodeficiency developing Hodgkin lymphoma shared a distinctive T cell profile, differing from immunocompetent lymphoma cases. Centralized histologic re-evaluation reclassified several presumed lymphoma as nonneoplastic/reactive hyperplasia and identified Castleman-like and germinal center transformation patterns in nonneoplastic/reactive LPD. Notably, elevated blood IgM and circulating T follicular helper cells mirrored IgM deposits and PD-1+ T cells in lymph nodes. These findings highlight the importance of an integrated approach involving clinical, genetic, and pathological reviews to improve IEI diagnosis and avoid overtreatment.

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Publication Details

Journal
Journal of Human Immunity
Published
2025-12-23
DOI
https://doi.org/10.70962/jhi.20250174
Citations
1
Primary Topic
Immunodeficiency and Autoimmune Disorders
Type
article
Field-Weighted Citation Impact
0.80
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article

Lymphoproliferation in inborn errors of immunity: From challenging diagnosis to histologic revision

Rita de Cássia Fernandes Gonçalves de Vito, Veronica Santilli, Emma Concetta Manno, R. Masetti et al.
1 citations
Journal of Human Immunity
Immunodeficiency and Autoimmune Disorders
0.80
article

Lymphoproliferation in inborn errors of immunity: From challenging diagnosis to histologic revision

Rita de Cássia Fernandes Gonçalves de Vito, Veronica Santilli, Emma Concetta Manno, R. Masetti, Andrea Finocchi, Silvia Di Cesare, Donato Amodio, Mattia Moratti, Riccardo Ciudino, Edoardo Muratore, Enrico Attardi, Beatrice Rivalta, Cristina Cifaldi, Elena Facchini, Gigliola Di Matteo, Samuele Naviglio, Antonello Cardoni, Alessandro Broccoli, Paola Selva, S. Ferrari, Francesca Conti, Rita Alaggio, Pier Luigi Zinzani, Elena Sabattini, Cinzia Milito, Nicola Cotugno, Chiara Mengoli, Alberto Tommasini, Marcello Lanari
article en
1 citations

Abstract

Inborn errors of immunity (IEI) are genetic disorders that not only heighten infection risk but also disrupt immune regulation, frequently leading to lymphoid tissue overgrowth known as lymphoid proliferations (LPD). We retrospectively reviewed 38 patients with genetically or clinically confirmed IEI and persistent LPD, comparing those with nonneoplastic/reactive hyperplasia to those who developed overt lymphoid neoplasm (lymphoma). Overall, 26% developed lymphoma—predominantly classical Hodgkin lymphoma or diffuse large B cell lymphoma—often after earlier IEI onset. Immunophenotyping and principal component analysis revealed that patients with common variable immunodeficiency developing Hodgkin lymphoma shared a distinctive T cell profile, differing from immunocompetent lymphoma cases. Centralized histologic re-evaluation reclassified several presumed lymphoma as nonneoplastic/reactive hyperplasia and identified Castleman-like and germinal center transformation patterns in nonneoplastic/reactive LPD. Notably, elevated blood IgM and circulating T follicular helper cells mirrored IgM deposits and PD-1+ T cells in lymph nodes. These findings highlight the importance of an integrated approach involving clinical, genetic, and pathological reviews to improve IEI diagnosis and avoid overtreatment.

Journal of Human ImmunityVol. 2(2)
University of Rome Tor Vergata (IT), University of Trieste (IT), IRCCS Materno Infantile Burlo Garofolo (IT), Istituto di Ematologia di Bologna (IT), Azienda USL di Bologna (IT), Bambino Gesù Children's Hospital (IT), Sapienza University of Rome (IT), University of Bologna (IT)
Good health and well-being
Openalex Percentile: Top 20%
Immunodeficiency and Autoimmune Disorders
0.80
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