# Resolution of Colchicine-Resistant, Corticosteroid-Dependent Acute Idiopathic Recurrent Pericarditis With Rilonacept: A Case Report

**Authors:** Satyatejas G Reddy, Samson L Mumber, Rahul Garg

PMC · DOI: 10.7759/cureus.82325 · Cureus · 2025-04-15

## TL;DR

A 55-year-old woman with persistent pericarditis unresponsive to standard treatments improved significantly after using rilonacept, an IL-1 inhibitor.

## Contribution

This case report demonstrates rilonacept's effectiveness in treating corticosteroid-dependent, colchicine-resistant acute idiopathic recurrent pericarditis.

## Key findings

- Rilonacept resolved symptoms and controlled inflammation in a patient resistant to colchicine and corticosteroids.
- The patient showed sustained improvement at a 12-month follow-up after rilonacept treatment.
- The case highlights rilonacept as a potential alternative for refractory pericarditis cases.

## Abstract

Pericarditis, the most common disease of the pericardium, is characterized by pleuritic, sharp, stabbing chest pain that worsens with breathing. Pericarditis can arise from various causes, including viral infections, malignancies, and drug reactions, though the cause often remains idiopathic. Treatment typically involves nonsteroidal anti-inflammatory drugs (NSAIDs), colchicine, and/or corticosteroids. In rare cases, biologic therapy may be required. Rilonacept, a recently approved interleukin-1 (IL-1) inhibitor for recurrent pericarditis, has shown promise in alleviating symptoms and preventing recurrence. Unlike NSAIDs, which inhibit cyclooxygenase enzymes, and colchicine, which disrupts microtubule assembly and inflammatory chemotaxis, rilonacept binds IL-1 and blocks proinflammatory signaling cascades. Additionally, while long-term corticosteroids do inhibit proinflammatory cytokines, they are known to have a host of long-term side effects, including osteoporosis and hyperglycemia. The efficacy of rilonacept across various stages of pericardial inflammation and in all recurrent cases remains uncertain. We report a case of idiopathic acute recurrent pericarditis in a 55-year-old South Asian woman. Eight months after the initial diagnosis, she experienced rising inflammatory markers and intermittent fevers despite treatment with ibuprofen and colchicine. Her condition progressed to corticosteroid dependence and marginal pericardial calcification, identified via an echocardiogram eight days after recurrent symptoms began. Symptom resolution and inflammation control were achieved with rilonacept, showing sustained success at a 12-month follow-up.

## Linked entities

- **Proteins:** IL1A (interleukin 1 alpha)
- **Chemicals:** colchicine (PubChem CID 2833), ibuprofen (PubChem CID 3672)
- **Diseases:** pericarditis (MONDO:0005904)

## Full-text entities

- **Genes:** IL1B (interleukin 1 beta) [NCBI Gene 3553] {aka IL-1, IL1-BETA, IL1F2, IL1beta}, CRP (C-reactive protein) [NCBI Gene 1401] {aka PTX1}, IL1A (interleukin 1 alpha) [NCBI Gene 3552] {aka IL-1 alpha, IL-1A, IL1, IL1-ALPHA, IL1F1}
- **Diseases:** tuberculosis (TB) infection (MESH:D014376), acute renal failure (MESH:D058186), viral infections (MESH:D014777), dyspnea (MESH:D004417), cardiovascular disease (MESH:D002318), hyperglycemia (MESH:D006943), dyslipidemia (MESH:D050171), Hyperlipidemia (MESH:D006949), constrictive pericarditis (MESH:D010494), pericardial and pleural effusions (MESH:D010996), fatigue (MESH:D005221), pericardial calcification (MESH:D008476), myocardial strain (MESH:D013180), pericardial rub (MESH:D012135), chronic kidney disease (MESH:D051436), type 2 diabetes (MESH:D003924), Acute pericarditis (MESH:D010493), renal failure (MESH:D051437), Calcification (MESH:D002114), Cushing's syndrome (MESH:D003480), osteoporosis (MESH:D010024), cardiac tamponade (MESH:D002305), osteopenia (MESH:D001851), autoinflammatory diseases (MESH:D056660), pericardial effusion (MESH:D010490), bone loss (MESH:D001847), autoimmune (MESH:D001327), heart failure (MESH:D006333), pulmonary embolism (MESH:D011655), depression (MESH:D003866), myocardial infarction (MESH:D009203), infection (MESH:D007239), malignancies (MESH:D009369), cardiac disease (MESH:D006331), blood sugar dysregulation (MESH:D006402), hypertension (MESH:D006973), pain (MESH:D010146), tachycardia (MESH:D013610), Inflammation (MESH:D007249), chest pain (MESH:D002637), respiratory infections (MESH:D012141), disease (MESH:D004194), fevers (MESH:D005334), hypothyroidism (MESH:D007037), corticosteroid dependence (MESH:C565152), diabetes (MESH:D003920), adrenal suppression (MESH:D000310), fractures (MESH:D050723)
- **Chemicals:** calcium (MESH:D002118), prednisone (MESH:D011241), aspirin (MESH:D001241), lipid (MESH:D008055), Colchicine (MESH:D003078), vitamin D (MESH:D014807), steroid (MESH:D013256), ibuprofen (MESH:D007052), glucose (MESH:D005947)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

5 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12081125/full.md

## References

26 references — full list in the complete paper: https://tomesphere.com/paper/PMC12081125/full.md

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Source: https://tomesphere.com/paper/PMC12081125