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A case of immunoglobulin G4-related chronic sclerosing sialadenitis and dacryoadenitis associated with tuberculosis

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Modern Rheumatology

Abstract

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.

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Acknowledgments

We would like to thank John Gelblum for his critical reading of the manuscript. This article does not contributes to any conflict of interest.

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Correspondence to Mitsuhiro Kawano.

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Kawano, M., Yamada, K., Kakuchi, Y. et al. A case of immunoglobulin G4-related chronic sclerosing sialadenitis and dacryoadenitis associated with tuberculosis. Mod Rheumatol 19, 87–90 (2009). https://doi.org/10.1007/s10165-008-0127-z

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  • DOI: https://doi.org/10.1007/s10165-008-0127-z

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