Skip to main content Accessibility help

We use cookies to distinguish you from other users and to provide you with a better experience on our websites. Close this message to accept cookies or find out how to manage your cookie settings.

Close cookie message
×
Hostname: page-component-586b7cd67f-gb8f7 Total loading time: 0 Render date: 2024-11-27T20:19:30.227Z Has data issue: false hasContentIssue false

Section III - Mature Lymphoid Neoplasm

Published online by Cambridge University Press:  25 November 2023

Edited by
Silvia Tse Bunting ,
Xiayuan Liang ,
Michele E. Paessler  and
Satheesh Chonat
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
Get access
Type
Chapter
Information
Atlas of Pediatric Hematopathology , pp. 65 - 126
Publisher: Cambridge University Press
Print publication year: 2023

Access options

Get access to the full version of this content by using one of the access options below. (Log in options will check for institutional or personal access. Content may require purchase if you do not have access.)

References

References

Perkins, SL. Pediatric mature B-cell non-Hodgkin lymphomas. In Proytcheva, MA, ed. Diagnostic pediatric hematopathology. Cambridge: Cambridge University Press; 2011:395–428.CrossRefGoogle Scholar
Leoncini, L, Campo, E, Stein, H, Harris, NL, Jeffe, ES, Kluin, PM. Burkitt lymphoma. In Swerdlow, SH, Campo, E, Harris, NL, et al., eds. WHO classification of tumours of haematopoietic and lymphoid tissue. Revised 4th ed. Lyon: IARC Press; 2017:330–4.Google Scholar
Leoncini, L, Campo, E, Stein, H, Harris, NL, Jeffe, ES, Kluin, PM. 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. Revised 4th ed. Lyon: IARC Press; 2017:334.Google Scholar
Salaverria, I, Martin-Guerrero, I, Wagener, R, Kreuz, M, Kohler, CW, Richter, J, et al. A recurrent 11q aberration pattern characterizes a subset of MYC-negative high-grade B-cell lymphomas resembling Burkitt lymphoma. Blood. 2014 Feb 20; 123(8): 1187–98.CrossRefGoogle ScholarPubMed
Gascoyne, RD, Campo, E, Jaffe, ES, Chan, WC, Chan, JKC, Rosenwald, A, 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. Revised 4th ed. Lyon: IARC Press; 2017:291–7.Google Scholar
Poirel, HA, Cairo, MS, Heerema, NA, Swansbury, J, Auperin, A, Launay, E, et al. Specific cytogenetic abnormalities are associated with a significantly inferior outcome in children and adolescents with mature B-cell non-Hodgkin’s lymphoma: Results of the FAB/LMB 96 international study. Leukemia. 2009 Feb; 23(2): 323–31.CrossRefGoogle ScholarPubMed
Gaulard, P, Harris, NL, Pileri, SA, Stein, H, Kovrigina, AM, Jeffe, ES, et al. Primary mediastinal (thymic) large B-cell lymphoma. In Swerdlow, SH, Campo, E, Harris, NL, et al. WHO classification of tumours of haematopoietic and lymphoid tissues. Revised 4th ed. Lyon: IARC Press; 2017:314–16.Google Scholar
Savage, KJ, Monti, S, Kutok, JL, Cattoretti, G, Neuberg, D, De Leval, L, et al. The molecular signature of mediastinal large B-cell lymphoma differs from that of other diffuse large B-cell lymphomas and shares features with classical Hodgkin lymphoma. Blood. 2003 Dec 1; 102(12): 3871–9.CrossRefGoogle ScholarPubMed
Weniger, MA, Gesk, S, Ehrlich, S, Martin‐Subero, JI, Dyer, MJ, Siebert, R, et al. Gains of REL in primary mediastinal B‐cell lymphoma coincide with nuclear accumulation of REL protein. Genes Chromosomes Cancer. 2007 Apr; 46(4): 406–15.CrossRefGoogle ScholarPubMed
Jaffe, ES, Harris, NL, Swerdlow, SH, Ott, G, Nathwani, BN, De Jong, D, et al. Follicular lymphoma. In Swerdlow, SH, Campo, E, Harris, NL, et al., eds. WHO classification of tumours of haematopoietic and lymphoid tissue. Revised 4th ed. Lyon: 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. Revised 4th ed. Lyon: IARC Press; 2017: 278–9.Google Scholar
Liu, Q, Salaverria, I, Pittaluga, S, Jegalian, AG, Xi, L, Siebert, R, et al. Follicular lymphomas in children and young adults: A comparison of the pediatric variant with usual follicular lymphoma. Am J Surg Pathol. 2013 Mar; 37(3): 333–43.CrossRefGoogle Scholar
Campo, E, Pileri, SA, Jaffe, ES, Nathwani, BN, Stein, H, Muller-Hermelink, HK. Nodal marginal zone lymphoma. In Swerdlow, SH, Campo, E, Harris, NL, et al., eds. WHO classification of tumours of haematopoietic and lymphoid tissue. Revised 4th ed. Lyon: IARC Press; 2017:263–5.Google Scholar
Swerdlow, SH. Pediatric follicular lymphomas, marginal zone lymphomas, and marginal zone hyperplasia. Pathol Patterns Rev. 2004 Dec 1; 122(suppl 1): S98–S109.CrossRefGoogle ScholarPubMed
Quintanilla-Martinez, L, Sander, B, Chan, JK, Xerri, L, Ott, G, Campo, E, Swerdlow, SH. Indolent lymphomas in the pediatric population: Follicular lymphoma, IRF4/MUM1+ lymphoma, nodal marginal zone lymphoma and chronic lymphocytic leukemia. Virchows Archiv. 2016 Feb 1; 468(2): 141–57.CrossRefGoogle ScholarPubMed

References

Perkins, SL. Pediatric mature T-cell and NK-cell non-Hodgkin lymphomas. In Proytcheva, MA, ed. Diagnostic pediatric hematopathology. Cambridge: Cambridge University Press; 2011:429–64.Google Scholar
Falini, B, Lamant-Rochaix, L, Campo, E, Jeffe, ES, Gascoyne, RD, Stein, H, 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. Revised 4th ed. Lyon: IARC Press; 2017:413–18.Google Scholar
Liang, X, Branchford, B, Greffe, B, McGavran, L, Carstens, B, Meltesen, L, et al. Dual ALK and MYC rearrangements leading to an aggressive variant of anaplastic large cell lymphoma. J Pediatr Hematol/Oncol. 2013 Jul 1; 35(5): e209–e213.CrossRefGoogle Scholar
Feldman, AL, Harris, NL, Stein, H, Campo, E, Kinney, MC, Jeffe, ES, 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. Revised 4th ed. Lyon: IARC Press; 2017:418–21.Google Scholar
Lamant-Rochaix, L, Feldman, AL, Delsol, G, Brousset, P. 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, Savage, KJ. Anaplastic large cell lymphoma, ALK-negative. Crit Rev Oncol/Hematol. 2013 Feb 1; 85(2): 206–15.CrossRefGoogle ScholarPubMed
Chan, JKC, Quintanilla-Martinez, L, Ferry, JA. 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. Revised 4th ed. Lyon: IARC Press; 2017:368–71.Google Scholar
Wilberger, AC, Liang, X. Primary nonanaplastic peripheral natural killer/T-cell lymphoma in pediatric patients: An unusual distribution pattern of subtypes. Pediatr Dev Pathol. 2019 Mar; 22(2): 128–36.CrossRefGoogle ScholarPubMed
Pileri, SA, Weisenburger, DD, Sng, I, Nakamura, S, Muller-Hermelink, HK, Chan, WC, Jaffe, ES. Peripheral T-cell lymphoma, NOS. In Swerdlow, SH, Campo, E, Harris, NL, et al., eds. WHO classification of tumours of haematopoietic and lymphoid tissue. Revised 4th ed. Lyon: IARC Press; 2017:403–7.Google Scholar
Mellgren, K, Attarbaschi, A, Abla, O, Alexander, S, Bomken, S, Bubanska, E, et al. Non-anaplastic peripheral T cell lymphoma in children and adolescents: An international review of 143 cases. Ann Hematol. 2016 Aug; 95(8): 1295–305.CrossRefGoogle ScholarPubMed
Gaulard, P, Berti, E, Willemze, R, Petrella, T, Jaffe, ES. 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. Revised 4th ed. Lyon: IARC Press; 2017:401–2.Google Scholar
Beltraminelli, H, Leinweber, B, Kerl, H, Cerroni, L. 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 Jun 1; 31(4): 317–22.CrossRefGoogle ScholarPubMed
Quintanilla-Martinez, L, Ko, Y-H, Kimura, H, Jaffe, ES. 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. Revised 4th ed. Lyon: IARC Press; 2017:355–63.Google Scholar
Portsmore, S, Chakravorty, S, Oppong, E, Ahmad, R, Bain, BJ. Systemic EBV‐positive lymphoproliferative disease of childhood. Am J Hematol. 2015 Apr; 90(4): 355.CrossRefGoogle ScholarPubMed
Chen, G, Chen, L, Qin, X, Huang, Z, Xie, X, Li, G, Xu, B. Systemic EBV-positive lymphoproliferative disease of childhood with hemophagocytic syndrome. Int J Clin Exp Pathol. 2014 Sep 15; 7(10): 7110–33. eCollection 2014.Google ScholarPubMed

References

Stein, H, Pileri, SA, Weiss, LM, Poppema, S, Gascoyne, RD, Jaffe, ES. Hodgkin lymphomas. In Swerdlow, SH, Campo, E, Harris, NL, et al., eds. WHO classification of tumours of haematopoietic and lymphoid tissue. Revised 4th ed. Lyon: IARC Press; 2017:424–30.Google Scholar
Mihaela, O. Hodgkin lymphomas. In Proytcheva, MA, ed. Diagnostic pediatric hematopathology. Cambridge: Cambridge University Press; 2011:465–83.Google Scholar
Stein, H, Swerdlow, SH, Gascoyne, RD, Popperma, S, Jaffe, ES, Pileri, SA. Nodular lymphocyte predominant Hodgkin lymphoma. In Swerdlow, SH, Campo, E, Harris, NL, et al., eds. WHO classification of tumours of haematopoietic and lymphoid tissue. Revised 4th ed. Lyon: IARC Press; 2017:431–4.Google Scholar
Shiels, MS, Koritzinsky, EH, Clarke, CA, Suneja, G, Morton, LM, Engels, EA. Prevalence of HIV infection among US Hodgkin lymphoma cases. Cancer Epidemiol Prev Biomark. 2014 Feb 1; 23(2): 274–81.CrossRefGoogle ScholarPubMed
Zhou, XG, Sandvej, K, Li, PJ, Ji, XL, Yan, QH, Zhang, XP, et al. Epstein‐Barr virus (EBV) in Chinese pediatric Hodgkin disease: Hodgkin disease in young children is an EBV‐related lymphoma. Cancer. 2001 Sep 15; 92(6): 1621–31.3.0.CO;2-P>CrossRefGoogle ScholarPubMed
Stein, H, Piler, SA, MacLennan, KA, Poppema, S, Guenova, M, Gascoyne, RD, Jaffe, E. Classical Hodgkin lymphoma. In Swerdlow, SH, Campo, E, Harris, NL, et al., eds. WHO classification of tumours of haematopoietic and lymphoid tissue. Revised 4th ed. Lyon: IARC Press; 2017:435–42.Google Scholar
Morton, LM, Wang, SS, Devesa, SS, Hartge, P, Weisenburger, DD, Linet, MS. Lymphoma incidence patterns by WHO subtype in the United States, 1992–2001. Blood. 2006 Jan 1; 107(1): 265–76.CrossRefGoogle ScholarPubMed
Shimabukuro-Vornhagen, A, Haverkamp, H, Engert, A, Balleisen, L, Majunke, P, Heil, G, et al. Lymphocyte-rich classical Hodgkin’s lymphoma: Clinical presentation and treatment outcome in 100 patients treated within German Hodgkin’s study group trials. J Clin Oncol. 2005 Aug 20; 23(24): 5739–45.CrossRefGoogle ScholarPubMed
Fan, Z, Natkunam, Y, Bair, E, Tibshirani, R, Warnke, RA. Characterization of variant patterns of nodular lymphocyte predominant Hodgkin lymphoma with immunohistologic and clinical correlation. Am J Surg Pathol. 2003 Oct 1; 27(10): 1346–56.CrossRefGoogle ScholarPubMed
Franke, S, Wlodarska, I, Maes, B, Vandenberghe, P, Achten, R, Hagemeijer, A, De Wolf-Peeters, C. Comparative genomic hybridization pattern distinguishes T-cell/histiocyte-rich B-cell lymphoma from nodular lymphocyte predominance Hodgkin’s lymphoma. Am J Pathol. 2002 Nov 1; 161(5): 1861–7.CrossRefGoogle ScholarPubMed

References

Swerdlow, SH, Webber, SA, Chadburn, A, Ferry, LA. Post-transplant lymphoproliferative disorders. In Swerdlow, SH, Campo, E, Harris, NL, et al., eds. WHO classification of tumours of haematopoietic and lymphoid tissue. Revised 4th ed. Lyon: IARC Press; 2017:453–62.Google Scholar
Abed, N, Casper, JT, Camitta, BM, Margolis, D, Trost, B, Orentas, R, Chang, CC. Evaluation of histogenesis of B-lymphocytes in pediatric EBV-related post-transplant lymphoproliferative disorders. Bone Marrow Transplant. 2004 Feb; 33(3): 321–7.CrossRefGoogle ScholarPubMed
Nelson, BP, Nalesnik, MA, Bahler, DW, Locker, J, Fung, JJ, Swerdlow, SH. Epstein-Barr virus-negative post-transplant lymphoproliferative disorders: A distinct entity? Am J Surg Pathol. 2000 Mar 1; 24(3): 375–85.CrossRefGoogle ScholarPubMed
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 Jul; 24(7): 1341–9.CrossRefGoogle ScholarPubMed
Romero, S, Montoro, J, Guinot, M, Almenar, L, Andreu, R, Balaguer, A, et al. Post-transplant lymphoproliferative disorders after solid organ and hematopoietic stem cell transplantation. Leukemia Lymphoma. 2019 Jan 2; 60(1): 142–50.CrossRefGoogle ScholarPubMed
Vakiani, E, Nandula, SV, Subramaniyam, S, Keller, CE, Alobeid, B, Murty, VV, Bhagat, G. Cytogenetic analysis of B-cell posttransplant lymphoproliferations validates the World Health Organization classification and suggests inclusion of florid follicular hyperplasia as a precursor lesion. Hum Pathol. 2007 Feb 1; 38(2): 315–25.CrossRefGoogle ScholarPubMed
Epperly, R, Ozolek, J, Soltys, K, Cohen, D, Goyal, R, Friehling, E. Treatment of pediatric plasma cell myeloma type post‐transplant lymphoproliferative disorder with modern risk‐directed therapy. Pediatr Blood Cancer. 2018 Oct; 65(10): e27283.CrossRefGoogle ScholarPubMed
Adams, H, Campidelli, C, Dirnhofer, S, Pileri, SA, Tzankov, A. Clinical, phenotypic and genetic similarities and disparities between post-transplant and classical Hodgkin lymphomas with respect to therapeutic targets. Expert Opin Ther Targets. 2009 Oct 1; 13(10): 1137–45.CrossRefGoogle ScholarPubMed

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: 19–30.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: 69–86.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): 11–22.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): 597–610.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

Save book to Kindle

To save this book to your Kindle, first ensure [email protected] is added to your Approved Personal Document E-mail List under your Personal Document Settings on the Manage Your Content and Devices page of your Amazon account. Then enter the ‘name’ part of your Kindle email address below. Find out more about saving to your Kindle.

Note you can select to save to either the @free.kindle.com or @kindle.com variations. ‘@free.kindle.com’ emails are free but can only be saved to your device when it is connected to wi-fi. ‘@kindle.com’ emails can be delivered even when you are not connected to wi-fi, but note that service fees apply.

Find out more about the Kindle Personal Document Service.

Available formats
×

Save book to Dropbox

To save content items to your account, please confirm that you agree to abide by our usage policies. If this is the first time you use this feature, you will be asked to authorise Cambridge Core to connect with your account. Find out more about saving content to Dropbox.

Available formats
×

Save book to Google Drive

To save content items to your account, please confirm that you agree to abide by our usage policies. If this is the first time you use this feature, you will be asked to authorise Cambridge Core to connect with your account. Find out more about saving content to Google Drive.

Available formats
×