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Chapter 12 - Immunodeficiency-Associated Lymphoproliferative Disorders

from Section III - Mature Lymphoid Neoplasm

Published online by Cambridge University Press:  25 November 2023

Silvia Tse Bunting
Affiliation:
Cleveland Clinic Florida Weston
Xiayuan Liang
Affiliation:
University of Colorado
Michele E. Paessler
Affiliation:
University of Pennsylvania School of Medicine
Satheesh Chonat
Affiliation:
Emory University, Atlanta
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Summary

Immunodeficiency-associated lymphoproliferative disorders (IA-LPDs) encompass a heterogeneous group of disorders that stem from diverse clinical settings and underlying disorders. These disorders may be benign lymphoproliferations to aggressive lymphomas. The World Health Organization (WHO) broadly classifies IA-LPDs into four groups: posttransplant lymphoproliferative disorders (PTLDs), lymphomas associated with HIV, lymphoproliferations associated with primary immune disorders, and other iatrogenic lymphoproliferative disorders. This chapter focuses on IA-LPDs of primary immune deficiencies seen commonly in the pediatric population, HIV-associated lymphoma, and iatrogenic lymphoproliferations.

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Publisher: Cambridge University Press
Print publication year: 2023

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References

Bonilla, FA, Khan, DA, Ballas, ZK, Chinen, J, Frank, MM, Hsu, JT, et al. Practice parameter for the diagnosis and management of primary immunodeficiency. J Allergy Clin Immunol. 2015; 136(5): 1186–205.CrossRefGoogle ScholarPubMed
Szczawińska-Poplonyk, A, Ossowska, L, Jończyk-Potoczna, K. Granulomatous liver disease in ataxia-telangiectasia with the hyper-IgM phenotype: A case report. Front Pediatr. 2020; 8: 570330.CrossRefGoogle ScholarPubMed
Rothblum-Oviatt, C, Wright, J, Lefton-Greif, MA, McGrath-Morrow, SA, Crawford, TO, Lederman, HM. Ataxia telangiectasia: A review. Orphanet J Rare Dis. 2016; 11(1): 159. https://doi.org/10.1186/s13023-016-0543-7.CrossRefGoogle ScholarPubMed
Yazdani, R, Fekrvand, S, Shahkarami, S, Azizi, G, Moazzami, B, Abolhassani, H, et al. The hyper IgM syndromes: Epidemiology, pathogenesis, clinical manifestations, diagnosis and management. Clin Immunol. 2019; 198: 1930.CrossRefGoogle ScholarPubMed
Aluri, J, Desai, M, Gupta, M, Dalvi, A, Terance, A, Rosenzweig, SD, et al. Clinical, immunological, and molecular findings in 57 patients with severe combined immunodeficiency (SCID) from India. Front Immunol. 2019; 10: 23.CrossRefGoogle ScholarPubMed
Ghafoor, A, Joseph, SM. Making a diagnosis of common variable immunodeficiency: A review. Cureus. 2020; 12(1): e6711.Google ScholarPubMed
Romberg, N, Lawrence, MG. Birds of a feather: Common variable immune deficiencies. Ann Allergy Asthma Immunol. 2019; 123(5): 461–7.CrossRefGoogle ScholarPubMed
Arnold, DE, Heimall, JR. A review of chronic granulomatous disease. Adv Ther. 2017; 34(12): 2543–57.CrossRefGoogle ScholarPubMed
Horwitz, M, Benson, KF, Person, RE, Aprikyan, AG, Dale, DC. Mutations in ELA2, encoding neutrophil elastase, define a 21-day biological clock in cyclic haematopoiesis. Nat Genet. 1999; 23(4): 433–6.CrossRefGoogle ScholarPubMed
Tidow, N, Pilz, C, Teichmann, B, Müller-Brechlin, A, Germeshausen, M, Kasper, B, et al. Clinical relevance of point mutations in the cytoplasmic domain of the granulocyte colony-stimulating factor receptor gene in patients with severe congenital neutropenia. Blood. 1997; 89(7): 2369–75.CrossRefGoogle ScholarPubMed
George, MR. Hemophagocytic lymphohistiocytosis: Review of etiologies and management. J Blood Med. 2014; 5: 6986.CrossRefGoogle ScholarPubMed
Fisher, GH, Rosenberg, FJ, Straus, SE, Dale, JK, Middleton, LA, Lin, AY, et al. Dominant interfering FAS gene mutations impair apoptosis in a human autoimmune lymphoproliferative syndrome. Cell. 1995; 81(6): 935–46.CrossRefGoogle Scholar
Maric, I, Pittaluga, S, Dale, JK, Niemela, JE, Delsol, G, Diment, J et al. Histologic features of sinus histiocytosis with massive lymphadenopathy in patients with autoimmune lymphoproliferative syndrome. Am J Surg Pathol. 2005; 29(7): 903–11.CrossRefGoogle ScholarPubMed
Swerdlow, SH, Campo, E, Harris, NL, Jaffe, ES, Pileri, SA, Stein, H, et al. Immunodeficiency-associated lymphoproliferative disorders. In Swerdlow, SH, Campo, E, Harris, NL, Jaffe, ES, Pileri, SA Stein, H, et al., eds. WHO classification of tumours and haematopoietic and lymphoid tissues. Revised 4th ed. Lyon: IARC Press; 2017: 449, 462.Google Scholar
Thai, A, Prindiville, T. Hepatosplenic T cell lymphoma and inflammatory bowel disease. J Crohns Colitis. 2010; 4(5): 1122.CrossRefGoogle ScholarPubMed
Amirifar, P, Yazdani, R, Shad, TM, Ghanadan, A, Abolhassani, H, Lavin, M, et al. Cutaneous granulomatosis and class switching defect as a presenting sign in ataxia-telangiectasia: First case from the national Iranian registry and review of the literature. Immunol Invest. 2020; 49(6): 597610.CrossRefGoogle ScholarPubMed
Romberg, N, Le Coz, C, Glauzy, S, Schickel, JN, Trofa, M, Nolan, BE, et al. Patients with common variable immunodeficiency with autoimmune cytopenias exhibit hyperplastic yet inefficient germinal center responses. J Allergy Clin Immunol. 2019; 143(1): 258–65.CrossRefGoogle ScholarPubMed

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