Skip to main content Accessibility help
×
Hostname: page-component-848d4c4894-xfwgj Total loading time: 0 Render date: 2024-06-26T00:01:36.810Z Has data issue: false hasContentIssue false

9 - Reactive lymphadenopathies

from Section 1 - General and non-neoplastic hematopathology

Published online by Cambridge University Press:  03 May 2011

Maria A. Proytcheva
Affiliation:
Northwestern University Feinberg School of Medicine
Maria A. Proytcheva
Affiliation:
Northwestern University Medical School, Illinois
Get access

Summary

Introduction

Lymphadenopathies occur frequently during childhood, and their incidence varies with age. In a majority of children, lymph node enlargement is transient, self-limited, and resolves without sequel, and lymph node biopsies are rarely performed. When a lymph node biopsy is performed, the primary goal of histologic examination is to determine the nature of the process: whether it is a malignant or benign, lymphoid or non-lymphoid proliferation.

This chapter focuses on reactive lymphoid proliferations in children. The chapter will first summarize key points in the development and functional anatomy of lymph nodes, then will discuss the epidemiology of pediatric lymphadenopathies and finally will describe the most frequent types of reactive lymphoid proliferations in children. Since characterization of all lymphadenopathies is beyond the scope of a single chapter, here we will focus on those entities that present major diagnostic challenges in distinguishing benign from malignant disorders, as well as those pediatric lymphadenopathies that are seen in conjunction with specific syndromes.

Embryonal development of lymph nodes

Lymph nodes, similarly to the other secondary lymphoid organs, have a specialized architecture and microenvironment promoting controlled interactions of immune cells in order to elicit a rapid and appropriate immune response to infectious agents. Knowledge of the development and functional anatomy of lymph nodes is important since many of the morphologic changes observed in reactive conditions reflect lymph node function and its role in the normal immune response.

Type
Chapter
Information
Publisher: Cambridge University Press
Print publication year: 2011

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

Randall, TD, Carragher, DM, Rangel-Moreno, J. Development of secondary lymphoid organs. Annual Review of Immunology. 2008;26:627–650.CrossRefGoogle ScholarPubMed
Blum, KS, Pabst, R. Keystones in lymph node development. Journal of Anatomy. 2006;209:585–595.CrossRefGoogle ScholarPubMed
Mebius, RE. Organogenesis of lymphoid tissues. Nature Reviews. Immunology. 2003;3:292–303. Erratum in Nature Reviews. Immunology. 2003;3:509.CrossRefGoogle ScholarPubMed
Drayton, DL, Liao, S, Mounzer, RH, Ruddle, NH. Lymphoid organ development: from ontogeny to neogenesis. Nature Immunology. 2006;7:344–353.CrossRefGoogle ScholarPubMed
Skandalakis, JE, Skandalakis, LJ, Skandalakis, PN. Anatomy of the lymphatics. Surgical Oncology Clinics of North America. 2007;16:1–16.CrossRefGoogle ScholarPubMed
Wilting, J, Papoutsi, M, Christ, B, et al. The transcription factor Prox1 is a marker for lymphatic endothelial cells in normal and diseased human tissues. The FASEB Journal. 2002;16:1271–1273.CrossRefGoogle ScholarPubMed
Yoshida, H, Naito, A, Inoue, J-I, et al. Different cytokines induce surface lymphotoxin-alphabeta on IL-7 receptor-alpha cells that differentially engender lymph nodes and Peyer's patches. Immunity. 2002;17:823–833.CrossRefGoogle ScholarPubMed
Blom, B, Spits, H. Development of human lymphoid cells. Annual Review of Immunology. 2006;24:287–320.CrossRefGoogle ScholarPubMed
Crivellato, E, Vacca, A, Ribatti, D. Setting the stage: an anatomist's view of the immune system. Trends in Immunology. 2004;25:210–217.CrossRefGoogle ScholarPubMed
Randolph, GJ, Ochando, J, Partida-Sanchez, S. Migration of dendritic cell subsets and their precursors. Annual Review of Immunology. 2008;26:293–316.CrossRefGoogle ScholarPubMed
Maclennan, ICM. Germinal centers. Annual Review of Immunology. 1994;12:117–139.CrossRefGoogle ScholarPubMed
Facchetti, F, Wolf-Peeters, C, Oord, JJ, Vos, R, Desmet, VJ. Plasmacytoid monocytes (so-called plasmacytoid T-cells) in Kikuchi's lymphadenitis. An immunohistologic study. American Journal of Clinical Pathology. 1989;92:42–50.CrossRefGoogle ScholarPubMed
Harris, NL, Bhan, AK. “Plasmacytoid T cells” in Castleman's disease. Immunohistologic phenotype. American Journal of Surgical Pathology. 1987;11:109–113.CrossRefGoogle ScholarPubMed
Marafioti, T, Paterson, JC, Ballabio, E, et al. Novel markers of normal and neoplastic human plasmacytoid dendritic cells. Blood. 2008;111:3778–3792.CrossRefGoogle ScholarPubMed
Krishnan, J, Danon, AD, Frizzera, G. Reactive lymphadenopathies and atypical lymphoproliferative disorders. American Journal of Clinical Pathology. 1993;99:385–396.CrossRefGoogle ScholarPubMed
Nield, LS, Kamat, D. Lymphadenopathy in children: when and how to evaluate. Clinical Pediatrics. 2004;43:25–33.CrossRefGoogle ScholarPubMed
Herzog, LW. Prevalence of lymphadenopathy of the head and neck in infants and children. Clinical Pediatrics. 1983;22:485–487.CrossRefGoogle ScholarPubMed
Knight, PJ, Mulne, AF, Vassy, . When is lymph node biopsy indicated in children with enlarged peripheral nodes?Pediatrics. 1982;69:391–396.Google ScholarPubMed
Moore, SW, Schneider, JW, Schaaf, HS. Diagnostic aspects of cervical lymphadenopathy in children in the developing world: a study of 1,877 surgical specimens. Pediatric Surgery International. 2003;19:240–244.CrossRefGoogle ScholarPubMed
Tsang, WY, Chan, JK. Fine-needle aspiration cytologic diagnosis of Kikuchi's lymphadenitis. A report of 27 cases. American Journal of Clinical Pathology. 1994;102:454–458.CrossRefGoogle ScholarPubMed
Tong, TR, Chan, OW, Lee, KC. Diagnosing Kikuchi disease on fine needle aspiration biopsy: a retrospective study of 44 cases diagnosed by cytology and 8 by histopathology. Acta Cytologica. 2001;45:953–957.CrossRefGoogle ScholarPubMed
Chiang, YC, Chen, RM, Chao, PZ, et al. Pediatric Kikuchi-Fujimoto disease masquerading as a submandibular gland tumor. International Journal of Pediatric Otorhinolaryngology. 2004;68:971–974.CrossRefGoogle ScholarPubMed
Perkins, SL, Segal, GH, Kjeldsberg, CR. Work-up of lymphadenopathy in children. Seminars in Diagnostic Pathology. 1995;12:284–287.Google ScholarPubMed
Kussick, SJ, Kalnoski, M, Braziel, RM, Wood, BL. Prominent clonal B-cell populations identified by flow cytometry in histologically reactive lymphoid proliferations. American Journal of Clinical Pathology. 2004;121:464–472.CrossRefGoogle ScholarPubMed
Orphanos, V, Anagnostou, D, Papadaki, T, et al. Detection of gene rearrangements in reactive lymphoid processes. Leukemia and Lymphoma. 1993;9:103–106.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. American Journal of Clinical Pathology. 2003;120:322–326.CrossRefGoogle ScholarPubMed
Howat, AJ, Variend, S. Epithelioid germinal centers. Archives of Pathology and Laboratory Medicine. 1989;113:451.Google ScholarPubMed
Howat, AJ, Variend, S. Nuclear fragmentation and epithelioid change of germinal centers in the lymphoid tissue of child deaths. Pediatric Pathology. 1986;5:125–134.CrossRefGoogle ScholarPubMed
Osborne, BM, Butler, JJ, Variakojis, D, et al. Reactive lymph node hyperplasia with giant follicles. American Journal of Clinical Pathology. 1982;78:493–499.CrossRefGoogle ScholarPubMed
Kojima, M, Nakamura, S, Shimizu, K, et al. Reactive lymphoid hyperplasia of the lymph nodes with giant follicles: a clinicopathologic study of 14 Japanese cases, with special reference to Epstein-Barr virus infection. International Journal of Surgical Pathology. 2005;13:267–272.CrossRefGoogle ScholarPubMed
Nosanchuk, JS, Schnitzer, B. Follicular hyperplasia in lymph nodes from patients with rheumatoid arthritis. A clinicopathologic study. Cancer. 1969;24:243–254.3.0.CO;2-C>CrossRefGoogle ScholarPubMed
Zhang, K, Biroschak, J, Glass, DN, et al. Macrophage activation syndrome in patients with systemic juvenile idiopathic arthritis is associated with MUNC13–4 polymorphisms. Arthritis & Rheumatism. 2008;58:2892–2896.CrossRefGoogle ScholarPubMed
Ferry, JA, Zukerberg, LR, Harris, NL. Florid progressive transformation of germinal centers. A syndrome affecting young men, without early progression to nodular lymphocyte predominance Hodgkin's disease. American Journal of Surgical Pathology. 1992;16:252–258.CrossRefGoogle ScholarPubMed
Osborne, BM, Butler, JJ, Gresik, MV. Progressive transformation of germinal centers: comparison of 23 pediatric patients to the adult population. Modern Pathology. 1992;5:135–140.Google ScholarPubMed
Segal, GH, Perkins, SL, Kjeldsberg, CR. Benign lymphadenopathies in children and adolescents. Seminars in Diagnostic Pathology. 1995;12:288–302.Google ScholarPubMed
Hicks, J, Flaitz, C. Progressive transformation of germinal centers: review of histopathologic and clinical features. International Journal of Pediatric Otorhinolaryngology. 2002;65:195–202.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. American Journal of Clinical Pathology. 2003;120:322–326.CrossRefGoogle ScholarPubMed
Brauninger, A, Yang, W, Wacker, HH, et al. B-cell development in progressively transformed germinal centers: similarities and differences compared with classical germinal centers and lymphocyte-predominant Hodgkin disease. Blood. 2001;97:714–719.CrossRefGoogle ScholarPubMed
Osborne, BM, Butler, JJ. Clinical implications of progressive transformation of germinal centers. American Journal of Surgical Pathology. 1984;8:725–733.CrossRefGoogle ScholarPubMed
Frizzera, G. Castleman's disease and related disorders. Seminars in Diagnostic Pathology. 1988;5:346–364.Google ScholarPubMed
Keller, AR, Hochholzer, L, Castleman, B. Hyaline-vascular and plasma-cell types of giant lymph node hyperplasia of the mediastinum and other locations. Cancer. 1972;29:670–683.3.0.CO;2-#>CrossRefGoogle ScholarPubMed
Harris, NL. Hypervascular follicular hyperplasia and Kaposi's sarcoma in patients at risk for AIDS. New England Journal of Medicine. 1984;310:462–463.Google Scholar
Nagai, K, Sato, I, Shimoyama, N. Pathohistological and immunohistochemical studies on Castleman's disease of the lymph node. Virchows Archiv – A, Pathological Anatomy & Histopathology. 1986;409:287–297.CrossRefGoogle ScholarPubMed
Leger-Ravet, MB, Peuchmaur, M, Devergne, O, et al. Interleukin-6 gene expression in Castleman's disease. Blood. 1991;78:2923–2930.Google ScholarPubMed
Yoshizaki, K, Matsuda, T, Nishimoto, N, et al. Pathogenic significance of interleukin-6 (IL-6/BSF-2) in Castleman's disease. Blood. 1989;74:1360–1367.Google Scholar
Hsu, SM, Waldron, JA, Xie, SS, Barlogie, B. Expression of interleukin-6 in Castleman's disease. Human Pathology. 1993;24:833–839.CrossRefGoogle ScholarPubMed
Chadburn, A, Cesarman, E, Nador, RG, Liu, EY, Knowles, DM. Kaposi's sarcoma-associated herpesvirus sequences in benign lymphoid proliferations not associated with human immunodeficiency virus. Cancer. 1997;80:788–797.3.0.CO;2-P>CrossRefGoogle Scholar
Parravicini, C, Corbellino, M, Paulli, M, et al. Expression of a virus-derived cytokine, KSHV vIL-6, in HIV-seronegative Castleman's disease. American Journal of Pathology. 1997;151:1517–1522.Google ScholarPubMed
Palma, DA, Dar, AR, Millington, SJ, et al. Castleman's disease in children: report of 2 cases and clinicopathologic review. Journal of Pediatric Hematology/Oncology. 2004;26:264–266.CrossRefGoogle ScholarPubMed
Parez, N, Bader-Meunier, B, Roy, CC, Dommergues, JP. Paediatric Castleman disease: report of seven cases and review of the literature. European Journal of Pediatrics. 1999;158:631–637.CrossRefGoogle ScholarPubMed
Smir, BN, Greiner, TC, Weisenburger, DD. Multicentric angiofollicular lymph node hyperplasia in children: a clinicopathologic study of eight patients. Modern Pathology. 1996;9:1135–1142.Google ScholarPubMed
Taylor, KL, Kaschula, RO. Castleman's disease in children: the experience of a children's hospital in Africa. Pediatric Pathology & Laboratory Medicine. 1995;15:857–868.CrossRefGoogle ScholarPubMed
Salisbury, JR. Castleman's disease in childhood and adolescence: report of a case and review of literature. Pediatric Pathology. 1990;10:609–615.CrossRefGoogle ScholarPubMed
Baserga, M, Rosin, M, Schoen, M, Young, G. Multifocal Castleman disease in pediatrics: case report. Journal of Pediatric Hematology/Oncology. 2005;27:666–669.CrossRefGoogle ScholarPubMed
Vasef, M, Katzin, WE, Mendelsohn, G, Reydman, M. Report of a case of localized Castleman's disease with progression to malignant lymphoma. American Journal of Clinical Pathology. 1992;98:633–636.CrossRefGoogle ScholarPubMed
Shetty, AK, Beaty, MW, McGuirt, WF Jr., et al. Kimura's disease: a diagnostic challenge. Pediatrics. 2002;110:e39.CrossRefGoogle ScholarPubMed
Swerdlow, SH. Pediatric follicular lymphomas, marginal zone lymphomas, and marginal zone hyperplasia. American Journal of Clinical Pathology. 2004;122(Suppl):S98–S109.Google ScholarPubMed
Frizzera, G, Murphy, SB. Follicular (nodular) lymphoma in childhood: a rare clinical-pathological entity. Report of eight cases from four cancer centers. Cancer. 1979;44:2218–2235.3.0.CO;2-D>CrossRefGoogle ScholarPubMed
Taddesse-Heath, L, Pittaluga, S, Sorbara, L, et al. Marginal zone B-cell lymphoma in children and young adults. American Journal of Surgical Pathology. 2003;27:522–531.CrossRefGoogle ScholarPubMed
Chikwava, K, Jaffe, R. Langerin (CD207) staining in normal pediatric tissues, reactive lymph nodes, and childhood histiocytic disorders. Pediatric & Developmental Pathology. 2004;7:607–614.CrossRefGoogle ScholarPubMed
Geissmann, F, Dieu-Nosjean, MC, Dezutter, C, et al. Accumulation of immature Langerhans cells in human lymph nodes draining chronically inflamed skin. Journal of Experimental Medicine. 2002;196:417–430.CrossRefGoogle ScholarPubMed
Hadinoto, V, Shapiro, M, Greenough, TC, et al. On the dynamics of acute EBV infection and the pathogenesis of infectious mononucleosis. Blood. 2008;111:1420–1427.CrossRefGoogle ScholarPubMed
Strickler, JG, Fedeli, F, Horwitz, CA, Copenhaver, CM, Frizzera, G. Infectious mononucleosis in lymphoid tissue. Histopathology, in situ hybridization, and differential diagnosis. Archives of Pathology & Laboratory Medicine. 1993;117:269–278.Google ScholarPubMed
Rushin, JM, Riordan, GP, Heaton, RB, et al. Cytomegalovirus-infected cells express Leu-M1 antigen. A potential source of diagnostic error. American Journal of Pathology. 1990;136:989–995.Google ScholarPubMed
Foucar, E, Rosai, J, Dorfman, R. Sinus histiocytosis with massive lymphadenopathy (Rosai-Dorfman disease): review of the entity. Seminars in Diagnostic Pathology. 1990;7:19–73.Google ScholarPubMed
Foucar, E, Rosai, J, Dorfman, RF, Eyman, JM. Immunologic abnormalities and their significance in sinus histiocytosis with massive lymphadenopathy. American Journal of Clinical Pathology. 1984;82:515–525.CrossRefGoogle ScholarPubMed
Maennle, DL, Grierson, HL, Gnarra, DG, Weisenburger, DD. Sinus histiocytosis with massive lymphadenopathy: a spectrum of disease associated with immune dysfunction. Pediatric Pathology. 1991;11:399–412.CrossRefGoogle ScholarPubMed
Maric, I, Pittaluga, S, Dale, JK, et al. Histologic features of sinus histiocytosis with massive lymphadenopathy in patients with autoimmune lymphoproliferative syndrome. American Journal of Surgical Pathology. 2005;29:903–911.CrossRefGoogle ScholarPubMed
Eisen, RN, Buckley, PJ, Rosai, J. Immunophenotypic characterization of sinus histiocytosis with massive lymphadenopathy (Rosai-Dorfman disease). Seminars in Diagnostic Pathology. 1990;7:74–82.Google Scholar
Lu, D, Estalilla, OC, Manning, JT Jr., Medeiros, LJ. Sinus histiocytosis with massive lymphadenopathy and malignant lymphoma involving the same lymph node: a report of four cases and review of the literature. Modern Pathology. 2000;13:414–419.CrossRefGoogle ScholarPubMed
Maia, DM, Dorfman, RF. Focal changes of sinus histiocytosis with massive lymphadenopathy (Rosai-Dorfman disease) associated with nodular lymphocyte predominant Hodgkin's disease. Human Pathology. 1995;26:1378–1382.CrossRefGoogle ScholarPubMed
Falk, S, Stutte, HJ, Frizzera, G. Hodgkin's disease and sinus histiocytosis with massive lymphadenopathy-like changes. Histopathology. 1991;19:221–224.CrossRefGoogle ScholarPubMed
Krzemieniecki, K, Pawlicki, M, Marganska, K, Parczewska, J. The Rosai-Dorfman syndrome in a 17-year-old woman with transformation into high-grade lymphoma. A rare disease presentation. Annals of Oncology. 1996;7:977.CrossRefGoogle Scholar
Weeks, DA, Beckwith, JB, Mierau, GW. Benign nodal lesions mimicking metastases from pediatric renal neoplasms: a report of the National Wilms' Tumor Study Pathology Center. Human Pathology. 1990;21:1239–1244.CrossRefGoogle ScholarPubMed
Yunis, EJ, Jaffe, R. Tamm-Horsfall protein in lymph nodes. Human Pathology. 1981;12:179–183.CrossRefGoogle ScholarPubMed
Kojima, M, Nakamura, S, Shimizu, K, et al. Inflammatory pseudotumor of lymph nodes: clinicopathologic and immunohistological study of 11 Japanese cases. International Journal of Surgical Pathology. 2001;9:207–214.CrossRefGoogle ScholarPubMed
Perrone, T, Wolf-Peeters, C, Frizzera, G. Inflammatory pseudotumor of lymph nodes. A distinctive pattern of nodal reaction. American Journal of Surgical Pathology. 1988;12:351–361.CrossRefGoogle ScholarPubMed
Moran, CA, Suster, S, Abbondanzo, SL. Inflammatory pseudotumor of lymph nodes: a study of 25 cases with emphasis on morphological heterogeneity. Human Pathology. 1997;28:332–338.CrossRefGoogle ScholarPubMed
Kutok, JL, Pinkus, GS, Dorfman, DM, Fletcher, CDM. Inflammatory pseudotumor of lymph node and spleen: an entity biologically distinct from inflammatory myofibroblastic tumor. Human Pathology. 2001;32:1382–1387.CrossRefGoogle ScholarPubMed
Chan, JK, Cheuk, W, Shimizu, M. Anaplastic lymphoma kinase expression in inflammatory pseudotumors. American Journal of Surgical Pathology. 2001;25:761–768.CrossRefGoogle ScholarPubMed
Arber, DA, Kamel, OW, Rijn, M, et al. Frequent presence of the Epstein-Barr virus in inflammatory pseudotumor. Human Pathology. 1995;26:1093–1098.CrossRefGoogle ScholarPubMed
New, NE, Bishop, PW, Stewart, M, Banerjee, SS, Harris, M. Inflammatory pseudotumour of lymph nodes. Journal of Clinical Pathology. 1995;48:37–40.CrossRefGoogle ScholarPubMed
Chan, JK, Warnke, RA, Dorfman, R. Vascular transformation of sinuses in lymph nodes. A study of its morphological spectrum and distinction from Kaposi's sarcoma. American Journal of Surgical Pathology. 1991;15:732–743.CrossRefGoogle ScholarPubMed
Bosch, X, Guilabert, A, Miquel, R, Campo, E. Enigmatic Kikuchi-Fujimoto disease: a comprehensive review. American Journal of Clinical Pathology. 2004;122:141–152.CrossRefGoogle ScholarPubMed
Tanaka, T, Ohmori, M, Yasunaga, S, et al. DNA typing of HLA class II genes (HLA-DR, -DQ and -DP) in Japanese patients with histiocytic necrotizing lymphadenitis (Kikuchi's disease). Tissue Antigens. 1999;54:246–253.CrossRefGoogle Scholar
Lin, HC, Su, CY, Huang, SC. Kikuchi's disease in Asian children. Pediatrics. 2005;115:e92–e96.CrossRefGoogle ScholarPubMed
Wang, TJ, Yang, YH, Lin, YT, et al. Kikuchi-Fujimoto disease in children: clinical features and disease course. Journal of Microbiology, Immunology & Infection. 2004;37:219–224.Google ScholarPubMed
O'Neill, D, O' Grady, J, Variend, S. Child fatality associated with pathological features of histiocytic necrotizing lymphadenitis (Kikuchi-Fujimoto disease). Pediatric Pathology & Laboratory Medicine. 1998;18:79–88.CrossRefGoogle Scholar
Lee, KY, Yeon, YH, Lee, BC. Kikuchi-Fujimoto disease with prolonged fever in children. Pediatrics. 2004;114:e752–e756.CrossRefGoogle ScholarPubMed
Scagni, P, Peisino, MG, Bianchi, M, et al. Kikuchi-Fujimoto disease is a rare cause of lymphadenopathy and fever of unknown origin in children: report of two cases and review of the literature. Journal of Pediatric Hematology/Oncology. 2005;27:337–340.CrossRefGoogle ScholarPubMed
Kuo, TT. Kikuchi's disease (histiocytic necrotizing lymphadenitis). A clinicopathologic study of 79 cases with an analysis of histologic subtypes, immunohistology, and DNA ploidy. American Journal of Surgical Pathology. 1995;19:798–809.CrossRefGoogle ScholarPubMed
Pileri, SA, Facchetti, F, Ascani, S, et al. Myeloperoxidase expression by histiocytes in Kikuchi's and Kikuchi-like lymphadenopathy. The American Journal of Pathology. 2001;159:915–924.CrossRefGoogle ScholarPubMed
Menasce, LP, Banerjee, SS, Edmondson, D, Harris, M. Histiocytic necrotizing lymphadenitis (Kikuchi-Fujimoto disease): continuing diagnostic difficulties. Histopathology. 1998;33:248–254.CrossRefGoogle ScholarPubMed
Chamulak, GA, Brynes, RK, Nathwani, BN. Kikuchi-Fujimoto disease mimicking malignant lymphoma. American Journal of Surgical Pathology. 1990;14:514–523.CrossRefGoogle ScholarPubMed
Emir, S, Gogus, S, Guler, E, Buyukpamukcu, M. Kikuchi-Fujimoto disease (histiocytic necrotizing lymphadenitis) confused with lymphoma in a child. Medical & Pediatric Oncology. 2001;37:546–548.CrossRefGoogle Scholar
Shapira, Y, Weinberger, A, Wysenbeek, AJ. Lymphadenopathy in systemic lupus erythematosus. Prevalence and relation to disease manifestations. Clinical Rheumatology. 1996;15:335–338.CrossRefGoogle ScholarPubMed
Kojima, M, Nakamura, S, Morishita, Y, et al. Reactive follicular hyperplasia in the lymph node lesions from systemic lupus erythematosus patients: a clinicopathological and immunohistological study of 21 cases. Pathology International. 2000;50:304–312.CrossRefGoogle ScholarPubMed
Cross, JT, Benton, HP. The roles of interleukin-6 and interleukin-10 in B cell hyperactivity in systemic lupus erythematosus. Inflammation Research. 1999;48:255–261.CrossRefGoogle Scholar
Windsor, JJ. Cat-scratch disease: epidemiology, aetiology and treatment. British Journal of Biomedical Science. 2001;58:101–110.Google ScholarPubMed
Bass, JW, Vincent, JM, Person, DA. The expanding spectrum of Bartonella infections: II. Cat-scratch disease. Pediatric Infectious Disease Journal. 1997;16:163–179.CrossRefGoogle ScholarPubMed
Carithers, HA. Cat-scratch disease. An overview based on a study of 1,200 patients. American Journal of Diseases of Children. 1985;139:1124–1133.CrossRefGoogle ScholarPubMed
Miller-Catchpole, R, Variakojis, D, Vardiman, JW, Loew, JM, Carter, J. Cat scratch disease. Identification of bacteria in seven cases of lymphadenitis. American Journal of Surgical Pathology. 1986;10:276–281.Google ScholarPubMed
Burns, JC, Glodé, MP. Kawasaki syndrome. Lancet. 2004;364:533–544.CrossRefGoogle ScholarPubMed
Newburger, JW, Taubert, KA, Shulman, ST, et al. Summary and abstracts of the Seventh International Kawasaki Disease Symposium: December 4–7, 2001, Hakone, Japan. Pediatric Research. 2003;53:153–157.Google ScholarPubMed
Rowley, AH, Baker, SC, Orenstein, JM, Shulman, ST. Searching for the cause of Kawasaki disease – cytoplasmic inclusion bodies provide new insight. Nature Reviews. Microbiology. 2008;6:394–401.CrossRefGoogle ScholarPubMed
Sung, RY, Ng, YM, Choi, KC, et al. Lack of association of cervical lymphadenopathy and coronary artery complications in Kawasaki disease. Pediatric Infectious Disease Journal. 2006;25:521–525.CrossRefGoogle ScholarPubMed
Giesker, DW, Pastuszak, WT, Forouhar, FA, et al. Lymph node biopsy for early diagnosis in Kawasaki disease. American Journal of Surgical Pathology. 1982;6:493–501.CrossRefGoogle ScholarPubMed
Amano, S, Hazama, F, Kubagawa, H, et al. General pathology of Kawasaki disease. On the morphological alterations corresponding to the clinical manifestations. Acta Pathologica Japonica. 1980;30:681–694.Google 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
×