1] Hamano H, Kawa S, Horiuchi A, et al. High serum IgG4 concentrations in patients with sclerosing pancreatitis[J]. N Engl J Med, 2001, 344(10):732-738.
[2] Stone JH, Zen Y, Deshpande V. IgG4-related disease[J]. N Engl J Med, 2012, 366(6):539-551.
[3] Himi T, Takano K, Yamamoto M, et al. A novel concept of Mikulicz’s disease as IgG4-related disease[J]. Auris Nasus Larynx, 2012, 39(1):9-17.
[4] Masaki Y, Sugai S, Umehara H. IgG4-related diseases including Mikulicz’s disease and sclerosing pancreatitis: diagnostic insights[J]. J Rheumatol, 2010, 37(7):1380-1385.
[5] Geyer JT, Deshpande V. IgG4-associated sialadenitis[J]. Curr Opin Rheumatol, 2011, 23(1):95-101.
[6] Takano K, Yamamoto M, Takahashi H, et al. Clinicopathologic similarities between Mikulicz disease and Kuttner tumor[J]. Am J Otolaryngol, 2010, 31(6):429-434.
[7] Bhatti RM, Stelow EB. IgG4-related disease of the head and neck[J]. Adv Anat Pathol, 2013, 20(1):10-16.
[8] Yamamoto M, Harada S, Ohara M, et al. Clinical and pathological differences between Mikulicz’s disease and Sjogren’s syndrome[J]. Rheumatology (Oxford), 2005, 44(2):227-234.
[9] Umehara H, Okazaki K, Masaki Y, et al. Comprehensive diagnostic criteria for IgG4-related disease (IgG4-RD), 2011[J]. Mod Rheumatol, 2012, 22(1):21-30.
[10] Takahashi H, Yamamoto M, Tabeya T, et al. The immunobiology and clinical characteristics of IgG4 related diseases[J]. J Autoimmun, 2012, 39(1-2):93-96.
[11] Harrison JD, Epivatianos A, Bhatia SN. Role of microliths in the aetiology of chronic submandibular sialadenitis: a clinicopathological investigation of 154 cases[J]. Histopathology, 1997, 31(3):237-251.
[12] Tiemann M, Teymoortash A, Schrader C, et al. Chronic sclerosing sialadenitis of the submandibular gland is mainly due to a T lymphocyte immune reaction[J]. Mod Pathol, 2002, 15(8):845-852.
13] Dooreck BS, Katz P, Barkin JS. Autoimmune pancreatitis in the spectrum of autoimmune exocrinopathy associated with sialoadenitis and anosmia[J]. Pancreas, 2004, 28(1):105-107.
[14] Kitagawa S, Zen Y, Harada K, et al. Abundant IgG4-positive plasma cell infiltration characterizes chronic sclerosing sialadenitis (Küttner’s tumor)[J]. Am J Surg Pathol, 2005, 29(6):783-791.
[15] Geyer JT, Ferry JA, Harris NL, et al. Chronic sclerosing sialadenitis (Küttner tumor) is an IgG4-associated disease[J]. Am J Surg Pathol, 2010, 34(2):202-210.
[16] Stone JH, Caruso PA, Deshpande V. Case records of the Massachusetts General Hospital. Case 24-2009. A 26-year-old woman with painful swelling of the neck[J]. N Engl J Med, 2009, 361(5):511-518.
[17] Ohta N, Kurakami K, Ishida A, et al. Clinical and pathological characteristics of IgG4-related sclerosing sialadenitis[J]. Laryngoscope, 2012, 122(3):572-577.
[18] Okazaki K, Umehara H. Are classification criteria for IgG4-RD now possible? The concept of IgG4-related disease and proposal of comprehensive diagnostic criteria in Japan[J]. Int J Rheumatol, 2012, 2012:357071.
[19] Harrison JD, Rodriguez-Justo M. Commentary on IgG4-related sialadenitis: Mikulicz’s disease, Kuttner’s tumour, and eponymy[J]. Histopathology, 2011, 58(7):1164-1166.
[20] Yamamoto M, Harada S, Ohara M, et al. Beneficial effects of steroid therapy for Mikulicz’s disease[J]. Rheumatology (Oxford), 2005, 44(10):1322-1323.
[21] Moriyama M, Tanaka A, Maehara T, et al. Clinical characteristics of Mikulicz’s disease as an IgG4-related disease[J]. Clin Oral Investig, 2012,[Epub ohead of print].
[22] Shimizu Y, Yamamoto M, Naishiro Y, et al. Necessity of early intervention for IgG4-related disease--delayed treatment induces fibrosis progression[J]. Rheumatology (Oxford), 2013,52(4):679-683. |