ArticleCase reports in rheumatology2026
A Rare Autoimmune Triad: Coexistence of Systemic Lupus Erythematosus, Sjögren's Syndrome, and Ankylosing Spondylitis: A Case Report.
Article in Case reports in rheumatology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.
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Abstract
Systemic lupus erythematosus (SLE), Sjögren's syndrome (SS), and ankylosing spondylitis (AS) are distinct immune-mediated diseases with different classification frameworks and usual treatment approaches. Coexistence of all three disorders in a single patient is rare and creates diagnostic and therapeutic challenges. We report a 40-year-old woman with longstanding SLE, SS associated with SLE, and subsequently recognized axial spondyloarthritis (axSpA)/AS. The patient fulfilled the 2019 ACR/EULAR classification criteria for SLE (total score ≥ 10), the 2016 ACR/EULAR classification criteria for primary SS (total score ≥ 4), and the 2009 ASAS classification criteria for axSpA through both the imaging and clinical arms. Conventional treatment options were limited by prior gastrointestinal bleeding with NSAIDs and concern for drug-induced lupus-like syndromes with TNF inhibitors. The patient remained stable on hydroxychloroquine 200 mg daily and was enrolled in a Phase 2 SLE clinical trial evaluating a JAK inhibitor. Treatment assignment was unknown during the blinded period; during the unblinded continuation phase, she was confirmed to be receiving upadacitinib 15 mg daily. Over a 6-month duration of confirmed upadacitinib exposure, clinical improvement in lupus- and sicca-related symptoms were observed, and follow-up MRI showed resolution of previously documented sacroiliitis. Although causality cannot be established from a single uncontrolled observation, the clinical and imaging improvement during confirmed upadacitinib exposure is hypothesis-generating and suggests that shared inflammatory pathways may warrant further investigation in selected overlap cases.
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