A case with overlapping features of IgG4-related autoimmune pancreatitis, Sjögren's syndrome and anti-aminoacyl-tRNA synthetase syndrome. (2nd January 2021)

• Record Type: Journal Article
• Authors: Yoshikawa, Masato; Muro, Yoshinao; Ogawa-Momohara, Mariko; Ito, Satoru; Takeichi, Takuya; Akiyama, Masashi
• Is Part Of: Modern rheumatology case reports. Volume 5:Number 1(2021)
• Page Start: 82
• Page End: 86
• Publication Date: 2021-01-02
• Subjects: Anti-aminoacyl-tRNA synthetase antibody -- anti-PL-7 antibody -- IgG4-related disease -- interstitial lung disease -- Sjögren's syndrome; Rheumatology -- Periodicals; 616.723005
• DOI: 10.1080/24725625.2020.1816675
• Languages: English
• ISSNs: 2472-5625

Abstract

Abstract: A 55-year-old man who had been diagnosed with autoimmune pancreatitis five years earlier was referred to our department because of finger swelling, finger stiffness and the presence of interstitial lung disease (ILD). The patient was diagnosed with Sjögren's syndrome according to the pathological findings of minor salivary glands and positive anti-SS-A antibodies. Later, at age 58, he was hospitalised due to the exacerbation of the ILD. Serum IgG4 level was checked and was found to be elevated (417 mg/dL). After the introduction of cyclosporine in addition to the prednisolone, at age 60, the ILD disease activity stabilised. However, at age 62, fever, myalgia and mechanic's hands appeared. His serum creatine kinase level was high, and magnetic resonance imaging showed inflammatory findings of muscle. In-house ELISA clarified that his serum carried anti-PL-7 antibody among anti-aminoacyl-tRNA synthetase antibodies. This is a unique case who had overlapping features of IgG4-related autoimmune pancreatitis, Sjögren's syndrome and anti-synthetase syndrome. Although the aetiology of the complications in this patient is obscure, autoimmunity might have played a significant role in the disease conditions and prognosis of the present case with IgG4-related disease.