A subset of rosai-dorfman disease exhibits features of IgG4-related disease

American Journal of Clinical Pathology

Volumn 139, Issue 5, 2013, Pages 622-632

  Zhang, Xuefeng ^a   Hyjek, Elizabeth ^a   Vardiman, James ^a  

^a UNIVERSITY OF CHICAGO MEDICAL CENTER   (United States)

Author keywords

IgG4; IgG4 related disease; Regulatory T cell; Rosai Dorfman disease

Indexed keywords

IMMUNOGLOBULIN G4;

ADOLESCENT; ADULT; ARTICLE; CELL INFILTRATION; CHILD; CLINICAL ARTICLE; CONTROLLED STUDY; FEMALE; HUMAN; HUMAN TISSUE; IMMUNOGLOBULIN G4 RELATED DISEASE; IMMUNOHISTOCHEMISTRY; MALE; PLASMA CELL; PRESCHOOL CHILD; PRIORITY JOURNAL; RECURRENT DISEASE; SCHOOL CHILD; SCLEROSIS; SINUS HISTIOCYTOSIS;

ADOLESCENT; ADULT; AGED; AUTOIMMUNE DISEASES; CHILD; CHILD, PRESCHOOL; FEMALE; HISTIOCYTOSIS, SINUS; HUMANS; HYPERGAMMAGLOBULINEMIA; IMMUNOGLOBULIN G; INFANT; LYMPH NODES; LYMPHATIC DISEASES; MALE; MIDDLE AGED; PLASMA CELLS; SCLEROSIS; T-LYMPHOCYTES, REGULATORY;

EID: 84878064933     PISSN: 00029173     EISSN: 19437722     Source Type: Journal    
DOI: 10.1309/AJCPARC3YQ0KLIOA     Document Type: Article

References (29)

1. Rosai J, Dorfman RF. Sinus histiocytosis with massive lymphadenopathy: a newly recognized benign clinicopathological entity. Arch Pathol. 1969;87:63-70.
2. Rosai J, Dorfman RF. Sinus histiocytosis with massive lymphadenopathy: a pseudolymphomatous benign disorder. Analysis of 34 cases. Cancer. 1972;30:1174-1188.
3. Kuo TT, Chen TC, Lee LY, et al. IgG4-positive plasma cells in cutaneous Rosai-Dorfman disease: an additional immunohistochemical feature and possible relationship to IgG4-related sclerosing disease. J Cutan Pathol. 2009;36:1069-1073.
4. Shrestha B, Sekiguchi H, Colby TV, et al. Distinctive pulmonary histopathology with increased IgG4-positive plasma cells in patients with autoimmune pancreatitis: report of 6 and 12 cases with similar histopathology. Am J Surg Pathol. 2009;33:1450-1462.
5. Chen TD, Lee LY. Rosai-Dorfman disease presenting in the parotid gland with features of IgG4-related sclerosing disease. Arch Otolaryngol Head Neck Surg. 2011;137:705-708.
6. Roberts SS, Attanoos RL. IgG4+ Rosai-Dorfman disease of the lung. Histopathology. 2010;56:662-664.
7. Kamisawa T, Okamoto A. IgG4-related sclerosing disease. World J Gastroenterol. 2008;14:3948-3955.
8. Kamisawa T, Takuma K, Egawa N, et al. Autoimmune pancreatitis and IgG4-related sclerosing disease. Nat Rev Gastroenterol Hepatol. 2010;7:401-409.
9. Umehara H, Okazaki K, Masaki Y, et al. Comprehensive diagnostic criteria for IgG4-related disease (IgG4-RD), 2011. Mod Rheumatol. 2012;22:21-30.
10. Gaitonde S. Multifocal, extranodal sinus histiocytosis with massive lymphadenopathy: an overview. Arch Pathol Lab Med. 2007;131:1117-1121.
11. Wimmer DB, Ko YH, Huh J, et al. Rosai-Dorfman disease: another possible IgG4 sclerosing disease? Mod Pathol. 2011;24:23A.
12. Shimosegawa T, Chari ST, Frulloni L, et al. International consensus diagnostic criteria for autoimmune pancreatitis: guidelines of the International Association of Pancreatology. Pancreas. 2011;40:352-358.
13. Dhall D, Suriawinata AA, Tang LH, et al. Use of immunohistochemistry for IgG4 in the distinction of autoimmune pancreatitis from peritumoral pancreatitis. Hum Pathol. 2010;41:643-652.
14. Deshpande V, Zen Y, Chan JK, et al. Consensus statement on the pathology of IgG4-related disease. Mod Pathol. 2012;25:1181-1192.
15. Aalberse RC, Stapel SO, Schuurman J, et al. Immunoglobulin G4: an odd antibody. Clin Exp Allergy. 2009;39:469-477.
16. Zen Y, Fujii T, Harada K, et al. Th2 and regulatory immune reactions are increased in immunoglobin G4-related sclerosing pancreatitis and cholangitis. Hepatology. 2007;45:1538-1546.
17. Kubota K, Kato S, Watanabe S, et al. Usefulness of endoscopic biopsy using FOXP3(+) Treg up-regulation in the duodenal papilla in the differential diagnosis between autoimmune pancreatitis and pancreatic cancer. J Hepatobiliary Pancreat Sci. 2011;18:414-421.
18. Pulsoni A, Anghel G, Falcucci P, et al. Treatment of sinus histiocytosis with massive lymphadenopathy (Rosai-Dorfman disease): report of a case and literature review. Am J Hematol. 2002;69:67-71.
19. Antonius JI, Farid SM, Baez-Giangreco A. Steroid-responsive Rosai-Dorfman disease. Pediatr Hematol Oncol. 1996;13:563-570.
20. Oka M, Kamo T, Goto N, et al. Successful treatment of Rosai-Dorfman disease with low-dose oral corticosteroid. J Dermatol. 2009;36:237-240.
21. Yilmaz S, Ture M, Maden A, et al. Extranodal Rosai-Dorfman disease with bilateral orbital involvement: report of a case treated with systemic steroid alone. Clin Ophthalmol. 2008;2:479-481.
22. Stine KC, Westfall C. Sinus histiocytosis with massive lymphadenopathy (SHML) prednisone resistant but dexamethasone sensitive. Pediatr Blood Cancer. 2005;44:92-94.
23. Al-Jahdali HH, Al-Shirawi NN, Bamefleh HS, et al. Sinus histiocytosis with massive lymphadenopathy (Rosai-Dorfman's disease) as cause of isolated hilar lymphadenopathy and complete remission after high dose steroid. Saudi Med J. 2008;29:763-765.
24. Ocheni S, Ibegbulam OG, Okafor OC, et al. Usefulness of oral corticosteroid in Rosai-Dorfman disease. Eur J Cancer Care (Engl). 2007;16:286-288.
25. McPherson CM, Brown J, Kim AW, et al. Regression of intracranial Rosai-Dorfman disease following corticosteroid therapy: case report. J Neurosurg. 2006;104:840-844.
26. Salim A, Williamson M, Barker F, et al. Steroid responsive cutaneous Rosai-Dorfman disease associated with uveitis and hypothyroidism. Clin Exp Dermatol. 2002;27:277-279.
27. Satter EK, Graham BS, Steger JW. Response of cutaneous Rosai-Dorfman disease to topical and intralesional steroids. Br J Dermatol. 2003;149:672-674.
28. Ottaviano G, Doro D, Marioni G, et al. Extranodal Rosai-Dorfman disease: involvement of eye, nose and trachea. Acta Otolaryngol. 2006;126:657-660.
29. Sakallioglu O, Gok F, Kalman S, et al. Minimal change nephropathy in a 7-year-old boy with Rosai-Dorfman disease. J Nephrol. 2006;19:211-214.