Association of IgG4-related disease and systemic rheumatic disorders

• Published in: European journal of internal medicine Vol. 111; pp. 63 - 68
• Main Authors: Batani, Veronica, Lanzillotta, Marco, Mahajne, Jasmin, Pedica, Federica, Palumbo, Diego, Venturini, Elena, Mapelli, Paola, Bossi, Paola, Dagna, Lorenzo, Della-Torre, Emanuel
• Format: Journal Article
• Language: English
• Published: Netherlands Elsevier B.V 01.05.2023
• Subjects: ANCA; Arthritis, Rheumatoid; Autoimmune Diseases - diagnosis; Humans; IgG4; IgG4-related disease; Immunoglobulin G4-Related Disease - complications; Immunoglobulin G4-Related Disease - diagnosis; Overlap; Retrospective Studies; Sarcoidosis; Takayasu arteritis; Vasculitis; IgG4-related disease; Vasculitis; Sarcoidosis; ANCA; IgG4; Takayasu arteritis; Overlap
• ISSN: 0953-6205; 1879-0828
• DOI: 10.1016/j.ejim.2023.03.015

•IgG4-RD can rarely occur together with pre-existing or concomitant systemic immune-mediated disorders.•IgG4-RD can occur in association with systemic autoimmune diseases and chronic granulomatous conditions.•Clinicians should consider the distinction between primary and secondary IgG4-RD. Autoimmune disorders can occur together especially in genetically predisposed individuals. We here aimed to assess the occurrence of IgG4-related disease (IgG4-RD) in association with other systemic immune-mediated conditions. We retrospectively analyzed the clinical records of patients with IgG4-RD followed at the IgG4-RD Clinic of San Raffaele Hospital (Milan, Italy) for pre-existing or concomitant immune-mediated disorders. IgG4-RD was diagnosed based on histological findings and on the 2011 Comprehensive Diagnostic criteria. Associated immune-mediated disorders were diagnosed based on available classification and/or diagnostic criteria. Two-hundred and thirty-four patients with a definitive diagnosis of IgG4-RD were included in this study. A pre-existing immune-mediated connective tissue disease was reported in 6/234 patients (3%): one case each of sarcoidosis, Takayasu arteritis (TA), eosinophilic granulomatosis with polyangitis (EGPA), and rheumatoid arthritis; and two cases of granulomatosis with polyangitis (GPA). Organs involved by IgG4-RD included the lungs, the pancreas, the peritoneum, lacrimal glands, meninges and orbits. Sarcoidosis, EGPA, and TA preceded the onset of IgG4-RD. GPA preceded IgG4-RD onset in one case and occurred simultaneously in the other case. Rheumatoid arthritis occurred together with IgG4-RD in one case. Our observation suggests that “secondary” IgG4-RD can present in the context of pre-existing systemic immune-mediated disorders and complicate systemic autoimmune diseases as well as chronic granulomatous conditions. Further studies are needed to define whether this peculiar clinical scenario is associated with different genetic backgrounds, pathological bases, and long-term outcomes.