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Section II - Normal and Non-neoplastic Hematolymphoid Diseases

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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Publisher: Cambridge University Press
Print publication year: 2023

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References

References

Deosthali, A, Donches, K, DelVecchio, M, Aronoff, S. Etiologies of pediatric cervical lymphadenopathy: A systematic review of 2687 subjects. Global Pediatric Health. 2019 Jul; 6: 2333794X19865440.CrossRefGoogle ScholarPubMed
Chang, CC, Osipov, V, Wheaton, S, Tripp, S, Perkins, SL. Follicular hyperplasia, follicular lysis, and progressive transformation of germinal centers: A sequential spectrum of morphologic evolution in lymphoid hyperplasia. Am J Clin Pathol. 2003 Sep 1; 120(3): 322–6.CrossRefGoogle ScholarPubMed
Ioachim, HL, Medeiros, LJ. The normal lymph node. In Medeiros, LJ, ed. Ioachim’s lymph node pathology. 4th ed. Philadelphia, PA: Wolters Kluwer/Lippincott Williams & Wilkins; 2009:114.Google Scholar
Shrestha, D, Dhakal, AK, KC SR, Shakya, A, Shah, SC, Shakya, H. Systemic lupus erythematosus and granulomatous lymphadenopathy. BMC Pediatrics. 2013 Dec; 13(1): 16.CrossRefGoogle ScholarPubMed
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(10): 3343–8.CrossRefGoogle ScholarPubMed

References

Greer, JP, Arber, DA, Glader, B, List, AF, Means, RT, Paraskevas, F, et al. Wintrobe’s clinical hematology. 13th ed. Philadelphia, PA: Lippincott Williams & Wilkins; 2014.Google Scholar
Bain, BJ, Clark, DM, Lampert, IA, Wilkins, BS. Bone marrow pathology. 3rd ed. Oxford: Blackwell Science; 2001.CrossRefGoogle Scholar
Foucar, K, Reichard, K, Czuchlewski, D. Bone marrow pathology. 4th ed. Hong Kong: American Society for Clinical Pathology Press; 2020.Google ScholarPubMed
Foucar, K, Viswanatha, DS, Wilson, CS. Non-neoplastic disorders of bone marrow. Atlas of nontumor pathology. Washington, DC: American Registry of Pathology; 2008.Google Scholar
Friebert, SE, Shepardson, LB, Shurin, SB, Rosenthal, GE, Rosenthal, NS. Pediatric bone marrow cellularity: Are we expecting too much? J Pediatr Hematol Oncol. 1998; 20(5): 439–43.CrossRefGoogle ScholarPubMed
Hartsock, RJ, Smith, EB, Petty, CS. Normal variations with aging of the amount of hematopoietic tissue in bone marrow from the Anterior Iliac Crest: A study made from 177 cases of sudden death examined by necropsy. Am J Clin Pathol. 1965; 43: 326–31.CrossRefGoogle ScholarPubMed
McKenna, RW, Washington, LT, Aquino, DB, Picker, LJ, Kroft, SH. Immunophenotypic analysis of hematogones (B-lymphocyte precursors) in 662 consecutive bone marrow specimens by 4-color flow cytometry. Blood. 2001; 98(8): 2498507.CrossRefGoogle ScholarPubMed
Rimsza, LM, Larson, RS, Winter, SS, Foucar, K, Chong, YY, Garner, KW, et al. Benign hematogone-rich lymphoid proliferations can be distinguished from B-lineage acute lymphoblastic leukemia by integration of morphology, immunophenotype, adhesion molecule expression, and architectural features. Am J Clin Pathol. 2000; 114(1): 6675.CrossRefGoogle ScholarPubMed
McKenna, RW, Asplund, SL, Kroft, SH. Immunophenotypic analysis of hematogones (B-lymphocyte precursors) and neoplastic lymphoblasts by 4-color flow cytometry. Leuk Lymphoma. 2004; 45(2): 277–85.CrossRefGoogle ScholarPubMed
Penchansky, L. Pediatric bone marrow. Berlin: Springer; 2004.CrossRefGoogle Scholar
Stuart-Smith, SE, Hughes, DA, Bain, BJ. Are routine iron stains on bone marrow trephine biopsy specimens necessary? J Clin Pathol. 2005; 58(3): 269–72.CrossRefGoogle Scholar

References

Oguz, A, Karadeniz, C, Temel, EA, Citak, EC, Okur, FV. Evaluation of peripheral lymphadenopathy in children. Pediatr Hematol Oncol. 2006; 23(7): 549–61.CrossRefGoogle ScholarPubMed
Rajasekaran, K, Krakovitz, P. Enlarged neck lymph nodes in children. Pediatr Clin North Am. 2013; 60(4): 923–36.CrossRefGoogle ScholarPubMed
Deosthali, A, Donches, K, DelVecchio, M, Aronoff, S. Etiologies of pediatric cervical lymphadenopathy: A systematic review of 2687 subjects. Glob Pediatr Health. 2019; 6: 2333794X19865440.Google ScholarPubMed
Chen, Y, Fu, YB, Xu, XF, Pan, Y, Lu, CY, Zhu, XL, et al. Lymphadenitis associated with cat-scratch disease simulating a neoplasm: Imaging findings with histopathological associations. Oncol Lett. 2018; 15(1): 195204.Google ScholarPubMed
Yuan, Y, Zhang, X, Xu, N, Wang, L, Li, F, Zhang, P, et al. Clinical and pathologic diagnosis and different diagnosis of syphilis cervical lymphadenitis. Int J Clin Exp Pathol. 2015; 8(10): 13635–8.Google ScholarPubMed
Cruz, AT, Ong, LT, Starke, JR. Mycobacterial infections in Texas children: A 5-year case series. Pediatr Infect Dis J. 2010; 29(8): 772–4.CrossRefGoogle ScholarPubMed
Reuss, AM, Wiese-Posselt, M, Weissmann, B, Siedler, A, Zuschneid, I, An der Heiden, M, et al. Incidence rate of nontuberculous mycobacterial disease in immunocompetent children: A prospective nationwide surveillance study in Germany. Pediatr Infect Dis J. 2009; 28(7): 642–4.CrossRefGoogle ScholarPubMed
Lewis, LL, Butler, KM, Husson, RN, Mueller, BU, Fowler, CL, Steinberg, SM, et al. Defining the population of human immunodeficiency virus-infected children at risk for Mycobacterium avium-intracellulare infection. J Pediatr. 1992; 121 (5 Pt 1): 677–83.CrossRefGoogle ScholarPubMed
Mishra, DP, Ramamurthy, S, Behera, SK. Histoplasmosis presenting as isolated cervical lymphadenopathy: A rare presentation. J Cytol. 2015; 32(3): 188–90.Google ScholarPubMed
Li, B, Zou, J, Wang, WY, Liu, SX. Toxoplasmosis presented as a submental mass: A common disease, uncommon presentation. Int J Clin Exp Pathol. 2015; 8(3): 3308–11.Google Scholar
Saxena, S, Kumar, S, Kharbanda, J. Toxoplasmosis submandibular lymphadenitis: Report of an unusual case with a brief review. J Oral Maxillofac Pathol. 2018; 22(1): 116–20.CrossRefGoogle ScholarPubMed
Pittaluga, S. Viral-associated lymphoid proliferations. Semin Diagn Pathol. 2013; 30(2): 130–6.CrossRefGoogle ScholarPubMed
Childs, CC, Parham, DM, Berard, CW. Infectious mononucleosis: The spectrum of morphologic changes simulating lymphoma in lymph nodes and tonsils.Am J Surg Pathol. 1987; 11(2): 122–32.CrossRefGoogle ScholarPubMed
Lum, EL, Schaenman, JM, DeNicola, M, Reddy, UG, Shen, JI, Pullarkat, ST. A case report of CMV lymphadenitis in an adult kidney transplant recipient. Transplant Proc. 2015; 47(1): 141–5.CrossRefGoogle Scholar
Staras, SA, Dollard, SC, Radford, KW, Flanders, WD, Pass, RF, Cannon, MJ. Seroprevalence of cytomegalovirus infection in the United States, 1988–1994. Clin Infect Dis. 2006; 43(9): 1143–51.CrossRefGoogle ScholarPubMed
Yusuf, H, Fields, E, Arrington-Sanders, R, Griffith, D, Agwu, AL. HIV preexposure prophylaxis among adolescents in the US: A review. JAMA Pediatr. 2020; 174(11): 1102–8.CrossRefGoogle ScholarPubMed
Posner, MR, Cavacini, LA, Emes, CL, Power, J, Byrn, R. Neutralization of HIV-1 by F105, a human monoclonal antibody to the CD4 binding site of gp120. J Acquir Immune Defic Syndr (1988). 1993; 6(1): 714.Google Scholar
Henn, A, Flateau, C, Gallien, S. Primary HIV infection: Clinical presentation, testing, and treatment. Curr Infect Dis Rep. 2017; 19(10): 37.CrossRefGoogle ScholarPubMed

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