ArticleCureus2025
Acute Pericarditis: An Isolated Initial Manifestation of Systemic Lupus Erythematosus (SLE).
Article in Cureus, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper, 1 of them a synthesis that pooled it.
What it found
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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
The trial behind it
Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.
Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.
Who cites it
1 citing paper in PubMed, 1 synthesis or guideline pooled it.
- Expanding the Therapeutic Landscape of Pericarditis: A Systematic Review of the Use of Conventional Immunosuppressants.Medicina (Kaunas, Lithuania) · 2026Pooled it
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
5 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Pericarditis is an inflammation of the pericardium that may arise from multiple etiologies, including autoimmune diseases such as systemic lupus erythematosus (SLE). Although cardiovascular involvement is relatively common in established SLE, acute pericarditis as an isolated and initial manifestation is rare and can delay diagnosis. Constrictive pericarditis, although an uncommon feature of lupus, has been rarely reported as an initial presentation without prior recurrent episodes of acute pericarditis, further underscoring the heterogeneity of pericardial involvement in SLE. We present the case of a 23-year-old male with no significant past medical history who arrived at the ED with acute precordial chest pain radiating to the neck and back, exacerbated by leaning forward, and accompanied by tachycardia, dyspnea, and fever. On admission, the ECG demonstrated ST-segment elevation in leads V2-V5 and first-degree atrioventricular block, while inflammatory markers were elevated with normal troponin levels. A pericardial friction rub was noted on physical examination, and cardiac MRI showed evidence of acute pericardial inflammation. During hospitalization, acute kidney injury of suspected primary renal origin prompted autoimmune testing, which revealed high-titer antinuclear antibodies, positive anti-dsDNA and anti-SSA antibodies, and hypocomplementemia, confirming the diagnosis of SLE. The patient was initially managed with nonsteroidal anti-inflammatory drugs and colchicine and subsequently treated with prednisone, mycophenolate mofetil, and hydroxychloroquine, achieving clinical improvement and stabilization without recurrence of symptoms. This case illustrates the importance of considering autoimmune etiologies in young patients presenting with idiopathic pericarditis. Early identification of SLE in such atypical presentations allows timely initiation of immunosuppressive therapy, reduces the risk of severe complications such as lupus nephritis or cardiac tamponade, and highlights the value of a multidisciplinary approach to improve prognosis.
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Registered trials
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