Skip to main content Accessibility help
×
Hostname: page-component-848d4c4894-hfldf Total loading time: 0 Render date: 2024-05-18T06:17:16.461Z Has data issue: false hasContentIssue false

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
Get access
Type
Chapter
Information
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

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

Save book to Kindle

To save this book to your Kindle, first ensure coreplatform@cambridge.org 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
×