A case of immunoglobulin G4-related chronic sclerosing sialadenitis and dacryoadenitis associated with tuberculosis
Mitsuhiro Kawano1 , Kazunori Yamada1 , Yasushi Kakuchi1 , Kiyoaki Ito1 , Ryoko Hamano1 , Hiroshi Fujii1 , Ryo Inoue1 , Masami Matsumura1 , Masayuki Takahira2 , Yoh Zen3 , Akihiro Yachie4 , Akikatsu Nakashima5, Masakazu Yamagishi1
9 May 2008
August 2008
15 October 2008
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We describe a 64-year-old woman with chronic sclerosing sialadenitis and dacryoadenitis, which developed during treatment for cervical lymph node tuberculosis. Anti-tuberculosis treatment did not improve the swelling in the lacrimal and submandibular glands, and a biopsy specimen of the lacrimal gland showed inflammation, with abundant lymphoid follicles with fibrosis and granuloma without caseous necrosis. Immunohistological examination of a repeat biopsy specimen showed abundant immunoglobulin (Ig) G4-positive plasma cell infiltration. Corticosteroid therapy improved the salivary gland swelling without reactivation of the tuberculosis. This case suggests that an abnormal immunological reaction to tuberculosis may be one of the etiological candidates for IgG4-related disease.
Immunoglobulin G4 (IgG4) - Mikulicz’s syndrome - Sclerosing dacryoadenitis - Sclerosing sialadenitis - Tuberculosis