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Section V - Mature Lymphoid Neoplasms

Published online by Cambridge University Press:  25 January 2024

Edited by
Xiayuan Liang ,
Bradford Siegele  and
Jennifer Picarsic
Xiayuan Liang
Affiliation:
Children’s Hospital of Colorado
Bradford Siegele
Affiliation:
Children’s Hospital of Colorado
Jennifer Picarsic
Affiliation:
Cincinnati Childrens Hospital Medicine Center
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Pediatric Pathology of Hematopoietic and Histiocytic Disorders , pp. 235 - 306
Publisher: Cambridge University Press
Print publication year: 2024

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References

References

Woessmann, W, Quintanilla‐Martinez, L. Rare mature B‐cell lymphomas in children and adolescents. Hematological Oncology. 2019;37:53–61.Google Scholar
Perkins, SL. Pediatric mature B-cell non-Hodgkin lymphomas. In: Proytcheva, MA, ed. Diagnostic pediatric hematopathology. Cambridge, UK: Cambridge University Press; 2011:395–428.Google Scholar
Leoncini, L, Campo, E, Stein, H, et al. Burkitt lymphoma. In: Swerdlow, SH, Campo, E, Harris, NL, et al., eds. WHO classification of tumours of haematopoietic and lymphoid tissue. Rev. 4th ed. Lyon, France: IARC Press; 2017:330–4.Google Scholar
Gascoyne, RD, Siebert, R, Connors, JM, et al. Burkitt’s lymphoma, and its mimics. In: Jaffe, ES, Arber, DA, Campo, E, et al., eds. Hematopathology. 2nd ed. Philadelphia, PA: Elsevier; 2017:447–64.Google Scholar
Dunleavy, K, Little, RF, Wilson, WH. Update on Burkitt lymphoma. Hematol Oncol Clin North Am. 2016;30:1333–43.Google Scholar
Ambrosio, MR, Navari, M, Di Lisio, L, et al. The Epstein Barr-encoded BART-6-3p microRNA affects regulation of cell growth and immuno response in Burkitt lymphoma. Infectious Agent Cancer. 2014;9:1–2.Google Scholar
Fish, K, Chen, J, Longnecker, R. Epstein-Barr virus latent membrane protein 2 A enhances MYC-driven cell cycle progression in a mouse model of B lymphoma. Blood. 2014;123:530–40.Google Scholar
Navid, F, Mosijczuk, AD, Head, DR, et al. Acute lymphoblastic leukemia with the (8;14)(q24; q32) translocation and FAB L3 morphology associated with a B-precursor immunophenotype: the Pediatric Oncology Group experience. Leukemia. 1999;13:135–41.Google Scholar
Gascoyne, R.D., Campo, E, Jaffe, ES, et al. Diffuse large B-cell Lymphoma, NOS. In: Swerdlow, SH, Campo, E, Harris, NL, et al., eds. WHO classification of tumours of haematopoietic and lymphoid tissue. Rev. 4th ed. Lyon, France:IARC Press;2017:291–7.,Google Scholar
Chan, ACL, Chan, JKC. Diffuse large B-cell lymphoma. In: Jaffe, ES, Arber, DA, Campo, E, et al., eds. Hematopathology. 2nd ed. Philadelphia, PA: Elsevier; 2017:415–45.Google Scholar
Li, S, Young, KH, Medeiros, LJ. Diffuse large B-cell lymphoma. Pathology. 2018;50:74–87.CrossRefGoogle ScholarPubMed
Hu, S, Xu-Monette, ZY, Balasubramanyam, A, et al. CD30 expression defines a novel subgroup of diffuse large B-cell lymphoma with favorable prognosis and distinct gene expression signature: a report from the International DLBCL Rituximab-CHOP Consortium Program Study. Blood. 2013;121:2715–24.Google Scholar
Gaulard, P, Harris, NL, Pileri, SA, et al. Primary mediastinal (thymic) large B-cell lymphoma. In: Swerdlow, SH, Campo, E, Harris, NL, et al., eds. WHO classification of tumours of haematopoietic and lymphoid tissues. Rev. 4th ed. Lyon, France: IARC Press; 2017:314–6.Google Scholar
Martelli, M, Ferreri, A, Di Rocco, A, et al. Primary mediastinal large B-cell lymphoma. Crit Rev Oncol Hematol. 2017;113:318–27.Google Scholar
Oschlies, I, Burkhardt, B, Salaverria, I, et al. Clinical, pathological and genetic features of primary mediastinal large B-cell lymphomas and mediastinal gray zone lymphomas in children. Haematologica. 2011;96:262–8.Google Scholar
Ott, G, Delabie, J, Gascoyne, RD, et al. T-cell/histiocyte-rich large B-cell lymphoma. In: Swerdlow, SH, Campo, E, Harris, NL, et al., eds. WHO classification of tumours of haematopoietic and lymphoid tissue. Rev. 4th ed. Lyon, France:IARC Press; 2017:298–9.Google Scholar
Pittaluga, S, Jaffe, ES. T-cell/histiocyte-rich large B-cell lymphoma. Haematologica. 2010;95:352–6.Google Scholar
Nam-Cha, SH, Roncador, G, Sanchez-Verde, L, et al. PD-1, a follicular T-cell marker useful for recognizing nodular lymphocyte-predominant Hodgkin lymphoma. Am J Surg Pathol. 2008;32:1252–7.Google Scholar
Hartmann, S, Döring, C, Vucic, E, et al. Array comparative genomic hybridization reveals similarities between nodular lymphocyte predominant Hodgkin lymphoma and T cell/histiocyte rich large B cell lymphoma. Br J Haematol. 2015;169:415–22.Google Scholar
Jaffe, ES, Harris, NL, Swerdlow, SH, et al. Follicular lymphoma. In: Swerdlow, SH, Campo, E, Harris, NL, et al.. eds. WHO classification of tumours of haematopoietic and lymphoid tissue. Rev. 4th ed. Lyon, France: IARC Press; 2017:266–73.Google Scholar
Jaffe, ES, Harris, NL, Siebert, R. Pediatric-type follicular lymphoma. In: Swerdlow, SH, Campo, E, Harris, NL, et al., eds. WHO classification of tumours of haematopoietic and lymphoid tissue. Rev. 4th ed. Lyon, France: IARC Press; 2017:278–9.Google Scholar
Ferry, JA, de Level, L, Louissaint, A Jr., et al. Follicular lymphoma. In: Jaffe, ES, Arber, DA, Campo, E, et al., eds. Hematopathology. 2nd ed. Philadelphia, PA: Elsevier; 2017:321–52.Google Scholar
Attarbaschi, A, Abla, O, Arias Padilla, L, et al. Rare non‐Hodgkin lymphoma of childhood and adolescence: A consensus diagnostic and therapeutic approach to pediatric‐type follicular lymphoma, marginal zone lymphoma, and nonanaplastic peripheral T‐cell lymphoma. Pediatr Blood Cancer. 2020;67:e28416.Google Scholar
Liu, Q, Salaverria, I, Pittaluga, S, et al. Follicular lymphomas in children and young adults: a comparison of the pediatric variant with usual follicular lymphoma. Am J Surg Pathol. 2013;37:333–43.Google Scholar
Pittaluga, S, Harris, NL, Siebert, R, et al. Large B-cell lymphoma with IRF4 rearrangement. In: Swerdlow, SH, Campo, E, Harris, NL, et al., eds. WHO classification of tumours of haematopoietic and lymphoid tissue. Rev. 4th ed. Lyon, France: IARC Press; 2017:280–1.Google Scholar
Sukswai, N, Lyapichev, K, Khoury, JD, et al. Diffuse large B-cell lymphoma variants: an update. Pathology. 2020;52:53–67.Google Scholar
Campo, E, Pileri, SA, Jaffe, ES, et al. Nodal marginal zone lymphoma. In: Swerdlow, SH, Campo, E, Harris, NL, et al., eds. WHO classification of tumours of haematopoietic and lymphoid tissue. Rev. 4th ed. Lyon, France: IARC Press; 2017:263–5.Google Scholar
Jaffe, ES. Nodal marginal zone lymphoma. In: Jaffe, ES, Arber, DA, Campo, E, et al., eds. Hematopathology. 2nd ed. Philadelphia, PA: Elsevier; 2017:383–96.Google Scholar
Attygalle, AD, Liu, H, Shirali, S, et al. Atypical marginal zone hyperplasia of mucosa-associated lymphoid tissue: a reactive condition of childhood showing immunoglobulin lambda light-chain restriction. Blood. 2004;104:3343–8.CrossRefGoogle ScholarPubMed
Kluin, PM, Harris, NL, Stein, H, et al. High-grade B-cell lymphoma. In: Swerdlow, SH, Campo, E, Harris, NL, et al., eds. WHO classification of tumours of haematopoietic and lymphoid tissue. Rev. 4th ed. Lyon, France: IARC Press; 2017:335–41.Google Scholar
Sesques, P, Johnson, NA. Approach to the diagnosis and treatment of high-grade B-cell lymphomas with MYC and BCL2 and/or BCL6 rearrangements. Blood. 2017;129:280–8.Google Scholar
Kluin, PM, Harris, NL, Stein, H, et al. B-cell lymphoma, unclassifiable, with features intermediate between diffuse large B-cell lymphoma and Burkitt lymphoma. In: Swerdlow, SH, Campo, E, Harris, NL, et al., eds. WHO classification of tumours of haematopoietic and lymphoid tissue. 4th ed. Lyon, France: IARC Press; 2008:265–6.Google Scholar
Jaffe, ES, Stein, H, Swerdlow, SH, et al. B-cell lymphoma, unclassifiable, with features intermediate between diffuse large B-cell lymphoma and classic Hodgkin lymphoma. In: Swerdlow, SH, Campo, E, Harris, NL, et al. eds. WHO classification of tumours of haematopoietic and lymphoid tissue. Rev. 4th ed. Lyon, France: IARC Press; 2017:342–4.Google Scholar
Fend, F. Classical Hodgkin’s lymphoma and related lesions. In: Jaffe, ES, Arber, DA, Campo, E, et al., eds. Hematopathology. 2nd ed. Philadelphia, PA: Elsevier; 2017:525–45.Google Scholar
Sarkozy, C, Copie-Bergman, C, Damotte, D, et al. Gray-zone lymphoma between CHL and large B-cell lymphoma. Am J Surg Pathol. 2019;43:341–51.Google Scholar
Leoncini, L, Campo, E, Stein, H, et al. Burkitt-like lymphoma with 11q aberration. In: Swerdlow, SH, Campo, E, Harris, NL, et al., eds. WHO classification of tumours of haematopoietic and lymphoid tissue. Rev. 4th ed.Lyon, France:IARC Press; 2017:334.Google Scholar
Salaverria, I, Martin-Guerrero, I, Wagener, R, et al. A recurrent 11q aberration pattern characterizes a subset of MYC-negative high-grade B-cell lymphomas resembling Burkitt lymphoma. Blood. 2014;123:1187–98.Google Scholar

References

Macon, WR. Peripheral T-cell lymphomas. Hematopathology. 2018;1:306–39.Google Scholar
Perkins, SL. Pediatric mature T-cell and NK-cell non-Hodgkin lymphomas. In: Proytcheva, MA, eds. Diagnostic pediatric hematopathology. Cambridge, UK: Cambridge University Press; 2011:429–64.Google Scholar
Attarbaschi, A, Abla, O, Arias Padilla, L, et al. Rare non‐Hodgkin lymphoma of childhood and adolescence: a consensus diagnostic and therapeutic approach to pediatric‐type follicular lymphoma, marginal zone lymphoma, and nonanaplastic peripheral T‐cell lymphoma. Pediatric Blood Cancer. 2020;67:e28416.Google Scholar
Falini, B, Lamant-Rochaix, L, Campo, E, et al. Anaplastic large cell lymphoma, ALK-positive. In: Swerdlow, SH, Campo, E, Harris, NL, et al., eds. WHO classification of tumours of haematopoietic and lymphoid tissue. Rev. 4th ed. Lyon, France: IARC Press; 2017:413–8.Google Scholar
Lamant-Rochaix, L, Feldman, AL, Delsol, G, et al. Anaplastic large cell lymphoma, ALK positive and ALK negative. In: Jaffe, ES, Arber, DA, Campo, E, et al., eds. Hematopathology. 2nd ed. Philadelphia, PA: Elsevier; 2017:673–91.Google Scholar
Montes-Mojarro, IA, Steinhilber, J, Bonzheim, I, et al. The pathological spectrum of systemic anaplastic large cell lymphoma (ALCL). Cancers. 2018;10:107.Google Scholar
Dunphy, CH, DeMello, DE, Gale, GB. Pediatric CD56+ anaplastic large cell lymphoma: a review of the literature. Arch Pathol Lab Med. 2006;130:1859–64.Google Scholar
Duyster, J, Bai, RY, Morris, SW. Translocations involving anaplastic lymphoma kinase (ALK). Oncogene. 2001;20:5623–37.Google Scholar
Liang, X, Branchford, B, Greffe, B, et al. Dual ALK and MYC rearrangements leading to an aggressive variant of anaplastic large cell lymphoma. J Pediatr Hematol Oncol. 2013;35:e209–13.Google Scholar
Feldman, AL, Harris, NL, Stein, H, et al. Anaplastic large cell lymphoma, ALK-negative. In: Swerdlow, SH, Campo, E, Harris, NL, et al., eds. WHO classification of tumours of haematopoietic and lymphoid tissue. Rev. 4th ed. Lyon, France: IARC Press; 2017:418–21.Google Scholar
Lamant-Rochaix, L, Feldman, AL, Delsol, G, et al. Anaplastic large cell lymphoma, ALK positive and ALK negative. In: Jaffe, E, Arber, DA, Campo, E, et al., eds. Hematopathology. 2nd ed. Philadelphia, PA: Elsevier;2017:673–91.Google Scholar
Ferreri, AJ, Govi, S, Pileri, SA, et al. Anaplastic large cell lymphoma, ALK-negative. Crit Rev Oncol Hematol. 2013;85:206–15.Google Scholar
Pileri, SA, Weisenburger, DD, Sng, I, et al. Peripheral T-cell lymphoma, NOS. In: Swerdlow, SH, Campo, E, Harris, NL, et al. eds. WHO classification of tumours of haematopoietic and lymphoid tissue. Rev. 4th ed. Lyon, France: IARC Press; 2017:403–7.Google Scholar
de Level, L. Peripheral T-cell lymphoma, not otherwise specified. In: Jaffe, E, Arber, DA, Campo, E, et al., eds. Hematopathology. 2nd ed. Philadelphia, PA: Elsevier;2017:641–57.Google Scholar
Mellgren, K, Attarbaschi, A, Abla, O, et al. Non-anaplastic peripheral T cell lymphoma in children and adolescents – an international review of 143 cases. Ann Hematol. 2016;95:1295–305.Google Scholar
Iqbal, J, Weisenburger, DD, Greiner, TC, et al. Molecular signatures to improve diagnosis in peripheral T-cell lymphoma and prognostication in angioimmunoblastic T-cell lymphoma. Blood. 2010;115:1026–36.Google Scholar
Chan, JKC, Quintanilla-Martinez, L, Ferry, JA, et al. Extranodal NK/T-cell lymphoma, nasal type. In: Swerdlow, SH, Campo, E, Harris, NL, et al. eds. WHO classification of tumours of haematopoietic and lymphoid tissue. Rev. 4th ed. Lyon, France: IARC Press; 2017:368–71.Google Scholar
Ko, YH, Chan, JKC, Quintanilla-Martinez, L. Virally associated T-cell and NK-cell lymphoma. In: Jaffe, E, Arber, DA, Campo, E, et al., eds. Hematopathology. 2nd ed. Philadelphia, PA: Elsevier;2017:565–98.Google Scholar
Gaulard, P, Jeffe, ES, Krenacs, L, et al. Hepatosplenic T-cell lymphoma. In: Swerdlow, SH, Campo, E, Harris, NL, et al., eds. WHO classification of tumours of haematopoietic and lymphoid tissue. Rev. 4th ed. Lyon, France: IARC Press; 2017:381–2.Google Scholar
Gaulard, P. Hepatosplenic T-cell lymphoma. In: Jaffe, E, Arber, DA, Campo, E, et al., eds. Hematopathology. 2nd ed. Philadelphia, PA: Elsevier;2017:631–9.Google Scholar
Belhadj, K, Reyes, F, Farcet, JP, et al. Hepatosplenic γδ T-cell lymphoma is a rare clinicopathologic entity with poor outcome: report on a series of 21 patients. Blood. 2003;102:4261–9.Google Scholar
Willemze, R, Paulli, M, Kadin, ME. Primary cutaneous CD30-positive T-cell lymphoproliferative disorders. In: Swerdlow, SH, Campo, E, Harris, NL, et al., eds. WHO classification of tumours of haematopoietic and lymphoid tissue. Rev. 4th ed.. Lyon, France: IARC Press; 2017:392–6.Google Scholar
Kempf, W, Kerl, K, Mitteldorf, C. Cutaneous CD30-positive T-cell lymphoproliferative disorders – clinical and histopathologic features, differential diagnosis, and treatment. Semin Cutan Med Surg. 2018;37:24–9.Google Scholar
Kadin, ME, Kempf, W. Primary cutaneous CD30-positive T-cell lymphoproliferative disorders. In: Jaffe, E, Arber, DA, Campo, E, et al., eds. Hematopathology. 2nd ed. Philadelphia, PA: Elsevier;2017:731–45.Google Scholar
Jaffe, ES, Gaulard, P, Cerroni, L. Subcutaneous panniculitis-like T-cell lymphoma. In: Swerdlow, SH, Campo, E, Harris, NL, et al., eds. WHO classification of tumours of haematopoietic and lymphoid tissue. Rev. 4th ed. Lyon, France: IARC Press; 2017:383–5.Google Scholar
Cerroni, L. Primary cutaneous T-cell lymphomas: Rare subtypes. In: Jaffe, E, Arber, DA, Campo, E, et al., eds. Hematopathology. 2nd ed. Philadelphia, PA: Elsevier;2017:747–60.Google Scholar
Gaulard, P, Berti, E, Willemze, R, et al. Primary cutaneous CD4+ small/medium T-cell lymphoproliferative disorder. In: Swerdlow, SH, Campo, E, Harris, NL, et al., eds. WHO classification of tumours of haematopoietic and lymphoid tissue. Rev. 4th ed. Lyon, France: IARC Press; 2017:401–2.Google Scholar
Beltraminelli, H, Leinweber, B, Kerl, H, et al. Primary cutaneous CD4+ small-/medium-sized pleomorphic T-cell lymphoma: a cutaneous nodular proliferation of pleomorphic T lymphocytes of undetermined significance? A study of 136 cases. Am J Dermatopathol. 2009;31:317–22.Google Scholar
Quintanilla-Martinez, L, Ko, YH, Kimura, H, et al. EBV-positive T-cell and NK-cell lymphoproliferative diseases of childhood. In: Swerdlow, SH, Campo, E, Harris, NL, et al., eds. WHO classification of tumours of haematopoietic and lymphoid tissue. Rev. 4th ed. Lyon, France: IARC Press; 2017:355–63.Google Scholar
Ko, YH, Chan, JKC, Quintanilla-Martinez, L. Virally associated T-cell and NK-cell neoplasms. In: Jaffe, E, Arber, DA, Campo, E, et al., eds. Hematopathology. 2nd ed. Philadelphia, PA: Elsevier;2017:565–98.Google Scholar
Cohen, JI, Manoli, I, Dowdell, K, et al. Hydroa vacciniforme–like lymphoproliferative disorder: an EBV disease with a low risk of systemic illness in whites. Blood. 2019;133:2753–64.Google Scholar
Liu, Y, Ma, C, Wang, G, et al. Hydroa vacciniforme–like lymphoproliferative disorder: Clinicopathologic study of 41 cases. J Am Acad Dermatol. 2019;81:534–40.Google Scholar

References

Stein, H, Pileri, SA, Weiss, LM, et al. Hodgkin lymphomas: Introduction. In: Swerdlow, SH, Campo, E, Harris, NL, et al., eds. WHO classification of tumours of haematopoietic and lymphoid tissue. Rev. 4th ed. Lyon, France:IARC Press; 2017:424–30.Google Scholar
Onciu, M. Hodgkin lymphomas. In: Proytcheva, MA, ed. Diagnostic pediatric hematopathology. Cambridge, UK: Cambridge University Press; 2011:465–83.Google Scholar
Jaffe, ES, Stein, H, Swerdlow, SH. Classic Hodgkin lymphomas. In: Swerdlow, SH, Campo, E, Harris, NL, et al., eds. WHO classification of tumours of haematopoietic and lymphoid tissue. Rev. 4th ed.Lyon, France:IARC Press; 2017:435.Google Scholar
Fend, F. Classical Hodgkin’s lymphoma and related lesions. In: Jaffe, ES, Arber, DA, Campo, E, et al., eds. Hematopathology. 2nd ed. Philadelphia, PA: Elsevier; 2017:525–45.Google Scholar
Mathas, S, Hartmann, S, Küppers, R. Hodgkin lymphoma: pathology and biology. Seminars Hematol. 2016; 53(3):139–47.Google Scholar
Mack, TM, Cozen, W, Shibata, DK, et al. Concordance for Hodgkin’s disease in identical twins suggesting genetic susceptibility to the young-adult form of the disease. N Engl J Med. 1995;332:413–9.Google Scholar
Horwitz, M, Wiernik, PH. Pseudoautosomal linkage of Hodgkin disease. Am J Hum Genet. 1999;65:1413–22.Google Scholar
Paltiel, O. Family matters in Hodgkin lymphoma. Leuk Lymphoma. 2008;49:1234–5.Google Scholar
Stein, H, Pileri, SA, MacLennan, KA, et al. Nodular sclerosis classic Hodgkin lymphoma. In: Swerdlow, SH, Campo, E, Harris, NL et al. eds. WHO classification of tumours of haematopoietic and lymphoid tissue. Rev. 4th ed. Lyon, France: IARC Press; 2017:435–7.Google Scholar
Weiss, LM, Poppema, S, Jaffe, E, et al. Mixed cellularity classic Hodgkin lymphoma. In: Swerdlow, SH, Campo, E, Harris, NL, et al., eds. WHO classification of tumours of haematopoietic and lymphoid tissue. Rev. 4th ed. Lyon, France:IARC Press; 2017:440.Google Scholar
Anagnostopoulos, I, Piris, MA, Isaacson, PG, et al. Lymphocyte-rich classic Hodgkin lymphoma. In: Swerdlow, SH, Campo, E, Harris, NL, et al., eds. WHO classification of tumours of haematopoietic and lymphoid tissue. Rev. 4th ed. Lyon, France:IARC Press; 2017:438–40.Google Scholar
Benharroch, D, Jaffe, E, Stein, H. Lymphocyte-depleted classic Hodgkin lymphoma. In: Swerdlow, SH, Campo, E, Harris, NL, et al., eds. WHO classification of tumours of haematopoietic and lymphoid tissue. Rev. 4th ed. Lyon, France: IARC Press; 2017:441–2.Google Scholar
Ansell, SM. Hodgkin lymphoma: A 2020 update on diagnosis, risk‐stratification, and management. Am J Hematol. 2020;95:978–89.Google Scholar
Stein, H, Swerdlow, SH, Gascoyne, RD, et al. Nodular lymphocyte predominant Hodgkin lymphoma. In: Swerdlow, SH, Campo, E, Harris, NL, et al., eds. WHO classification of tumours of haematopoietic and lymphoid tissue. Rev. 4th ed.Lyon, France:IARC Press; 2017:431–4.Google Scholar
Hartmann, S, Eichenauer, DA. Nodular lymphocyte predominant Hodgkin lymphoma: pathology, clinical course and relation to T-cell/histiocyte rich large B-cell lymphoma. Pathology. 2020;52:142–53.Google Scholar
Fan, Z, Natkunam, Y, Bair, E, et al. Characterization of variant patterns of nodular lymphocyte predominant Hodgkin lymphoma with immunohistologic and clinical correlation. Am J Surg Pathol. 2003;27:1346–56.Google Scholar
Boudová, L, Torlakovic, E, Delabie, J, et al. Nodular lymphocyte-predominant Hodgkin lymphoma with nodules resembling T-cell/histiocyte-rich B-cell lymphoma: differential diagnosis between nodular lymphocyte-predominant Hodgkin lymphoma and T-cell/histiocyte-rich B-cell lymphoma. Blood. 2003;102: 3753–8.Google Scholar
Franke, S, Wlodarska, I, Maes, B, et al. Comparative genomic hybridization pattern distinguishes T-cell/histiocyte-rich B-cell lymphoma from nodular lymphocyte predominance Hodgkin’s lymphoma. Am J Pathol. 2002;161:1861–7.Google Scholar

References

Onciu, M, van Krieken, JH. Immunodeficiency-associated lymphoproliferative disorders. In: Proytcheva, MA, ed.Diagnostic pediatric hematopathology. Cambridge, UK: Cambridge University Press; 2011:484–503.Google Scholar
Shabani, M, Nichols, KE, Rezaei, N. Primary immunodeficiencies associated with EBV-Induced lymphoproliferative disorders. Crit Rev Oncol Hematol. 2016;108:109–27.Google Scholar
Low, LK, Song, JY. B-cell lymphoproliferative disorders associated with primary and acquired immunodeficiency. Surg Pathol Clin. 2016;9:55–77.Google Scholar
van Krieken, JH, Onciu, M, Elenitoba-Johnson, KSJ, et al. Lymphoproliferative diseases associated with primary Immune disorders. In: Swerdlow, SH, Campo, E, Harris, NL, et al., eds. WHO classification of tumours of haematopoietic and lymphoid tissue. Rev. 4th ed.Lyon, France:IARC Press; 2017:444–8.Google Scholar
Aricò, M, Mussolin, L, Carraro, E, et al. Non‐Hodgkin lymphoma in children with an associated inherited condition: a retrospective analysis of the Associazione Italiana Ematologia Oncologia Pediatrica (AIEOP). Pediatr Blood Cancer. 2015;62:1782–9.Google Scholar
O’Malley, DP, George, TI, Orazi, A, et al. Congenital immunodeficiency diseases. In: Benign and reactive conditions of lymph node and spleen. Washington, DC: American Registry of Pathology in collaboration with the Armed Forces Institute of Pathology; 2009; 185–227.Google Scholar
Said, J, Cesarman, E, Rosenwald, A, et al. Lymphomas associated with HIV infection. In: Swerdlow, SH, Campo, E, Harris, NL, et al., eds. WHO classification of tumours of haematopoietic and lymphoid tissue. Rev. 4th ed. Lyon, France:IARC Press; 2017:449–52.Google Scholar
O’Malley, DP, George, TI, Orazi, A, et al. Viral lymphadenopathies. In: Benign and reactive conditions of lymph node and spleen. Washington, DC: American Registry of Pathology in collaboration with the Armed Forces Institute of Pathology; 2009;283–326.Google Scholar
Swerdlow, SH, Webber, SA, Chadburn, A, et al. Post-transplant lymphoproliferative disorders. In: Swerdlow, SH, Campo, E, Harris, NL, et al., eds. WHO classification of tumours of haematopoietic and lymphoid tissue. Rev. 4th ed. Lyon, France:IARC Press; 2017:453–62.Google Scholar
Swerdlow, S, Craig, FE. Iatrogenic immunodeficiency-associated lymphoproliferative disorders. In: Jaffe, ES, Arber, DA, Campo, E, et al., eds. Hematopathology. 2nd ed. Philadelphia, PA: Elsevier; 2017:1013–29.Google Scholar
Kalinova, L, Indrakova, J, Bachleda, P. Post-transplant lymphoproliferative disorder. Biomed Pap Med Fac Univ Palacky Olomouc Czech Repub. 2009;153:251–7.Google Scholar
Liu, L, Zhang, X, Feng, S. Epstein-Barr virus-related post-transplantation lymphoproliferative disorders after allogeneic hematopoietic stem cell transplantation. Biol Blood Marrow Transplant. 2018;24:1341–9.Google Scholar
Romero, S, Montoro, J, Guinot, M, et al. Post-transplant lymphoproliferative disorders after solid organ and hematopoietic stem cell transplantation. Leuk Lymphoma. 2019;60:142–50.Google Scholar
Nelson, BP, Nalesnik, MA, Bahler, DW, et al. Epstein-Barr virus-negative post-transplant lymphoproliferative disorders: a distinct entity? Am J Surg Pathol. 2000;24:375–85.Google Scholar
Gaulard, P, Swerdlow, SH, Harris, NL, et al. Other iatrogenic immunodeficiency-associated lymphoproliferative disorders. In: Swerdlow, SH, Campo, E, Harris, NL, et al., eds. WHO classification of tumours of haematopoietic and lymphoid tissue. Rev. 4th ed.Lyon, France: IARC Press; 2017:462–4.Google Scholar
Rosh, JR, Gross, T, Mamula, P, et al. Hepatosplenic T-cell lymphoma in adolescents and young adults with Crohn’s disease: a cautionary tale? Inflamm Bowel Dis. 2007;13:1024–30.Google Scholar

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