Abstract
Mikulicz’s disease (MD), an immunoglobulin G4 (IgG4)-related disease, is a fibrosis-associated inflammatory disease characterized by painless bilat- eral swelling of lacrimal and salivary glands. Although thrombocytopenia is associated with many rheumatologic disorders, it is rare in IgG4-related MD. This novel study aims to report a rare case of IgG4-related MD complicated with severe autoimmune thrombocytopenia without any hemato- logical malignancies and review all cases of IgG4-related disease associated with thrombocytopenia in the literature.
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Article Info
Published In
Journal
Archives of Rheumatology
Volume / Issue
Volume 34 · Issue 3
Pages
343-347
History
Published Online
September 30, 2019
License

This work is licensed under a Creative Commons Attribution 4.0 International License.
Copyright
Copyright (c) 2019 Shu LI, Cong DENG, Jinwei CHEN, Fen LI
Affiliations
Shu LI
Department of Rheumatology and Immunology, The Second Xiangya Hospital, Central South University, Changsha, China
Cong DENG
Department of Rheumatology and Immunology, The Second Xiangya Hospital, Central South University, Changsha, China
Jinwei CHEN
Department of Rheumatology and Immunology, The Second Xiangya Hospital, Central South University, Changsha, China
Fen LI
Department of Rheumatology and Immunology, The Second Xiangya Hospital, Central South University, Changsha, China
Cite this Article
Shu LI, Cong DENG, Jinwei CHEN, & Fen LI. (2019). Mikulicz’s Disease With Immune Thrombocytopenia: A New Immunoglobulin G4-Mediated Disorder and Literature Review. Archives of Rheumatology, 34(3), 343–347. https://doi.org/10.5606/ArchRheumatol.2019.7070
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