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Chronic constrictive pericarditis: a rare cardiac involvement in primary Sjögren's syndrome
Fabiana Duarte1, Luís Oliveira2, Tomás Fontes3
1Cardiology Department, Hospital of Divino Espírito Santo of Ponta Delgada, EPER, São Miguel Island, Avenida D. Manuel I 9500-370, Azores, Portugal. f.duarte@campus.ul.pt.
Insights
Constrictive pericarditis is rarely caused by primary Sjögren's syndrome. This case highlights the importance of clinical suspicion and imaging for diagnosing this rare autoimmune-related cardiac condition.
Area of Science:
- Cardiology
- Rheumatology
- Internal Medicine
Background:
- Constrictive pericarditis is a chronic condition with systemic inflammatory diseases as uncommon causes.
- Pericardial involvement is rarely reported in primary Sjögren's syndrome, typically with effusion or pericarditis.
Observation:
- A 48-year-old male with primary Sjögren's syndrome developed constrictive pericarditis over four years.
- Initial symptoms included pleural effusion and ascites, later progressing to dyspnea and abdominal distension.
- Imaging revealed pericardial thickening and effusion, leading to a diagnosis of constrictive pericarditis.
Findings:
- This case presents a rare association between primary Sjögren's syndrome and constrictive pericarditis.
- The diagnosis was challenging due to the insidious course and unusual evolution of the condition.
- Multimodality imaging and clinical suspicion were crucial for early identification.
Implications:
- Connective tissue disorders like primary Sjögren's syndrome should be considered in constrictive pericarditis, especially in younger patients without other risk factors.
- Early recognition and treatment are essential for managing this rare but serious condition.
- Long-term outcomes for constrictive pericarditis associated with primary Sjögren's syndrome remain uncertain.
Background:
Constrictive pericarditis represents a chronic condition and systemic inflammatory diseases are a known, yet uncommon, cause. Pericardial involvement is seldom reported in primary Sjögren's syndrome, usually occurring in association with pericardial effusion or pericarditis. We report a case of constrictive pericarditis with an insidious course and unusual evolution associated with primary Sjögren's syndrome. Due to the challenging nature of the diagnosis, clinical suspicion and multimodality imaging are essential for early identification and prompt initiation of treatment. Long-term outcomes remain uncertain. To the best of our knowledge, no other cases linking this autoimmune disease to constrictive pericarditis have been reported.
Case Presentation:
We present the case of a 48-year-old male patient with moderate alcohol habits and a history of two prior hospitalizations. On the first, the patient was diagnosed with primary Sjögren's syndrome after presenting with pleural effusion and ascites, and empirical corticosteroid regiment was initiated. On the second, two-years later, he was readmitted with complaints of dyspnea and abdominal distension. Thoracic computed tomography revealed a localized pericardial thickening and a thin pericardial effusion, both of which were attributed to his rheumatic disease. A liver biopsy showed hepatic peliosis, which was considered to be a consequence of glucocorticoid therapy. Diuretic therapy was adjusted to symptom-relief, and a tapering corticosteroid regimen was adopted. Four years after the initial diagnosis, the patient was admitted again with recurrent dyspnea, orthopnea and ascites. At this time, constrictive pericarditis was diagnosed and a partial pericardiectomy was performed. Although not completely asymptomatic, the patient reported clinical improvement since the surgery, but still with a need for baseline diuretic therapy.
Conclusion:
Albeit uncommon, connective tissue disorders, such as primary Sjögren's syndrome, should be considered as a potential cause of constrictive pericarditis, especially in young patients with no other classical risk factors for constriction. In this case, after excluding possible infectious, neoplastic and autoimmune conditions, a primary Sjögren´s syndrome in association with constrictive pericarditis was assumed. This case presents an interesting and challenging clinical scenario, highlighting the importance of clinical awareness and the use of multimodal cardiac imaging for early recognition and treatment.
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