A Case of Acute Pericarditis and Hypereosinophilia After Dupilumab Initiation

Dupilumab is a monoclonal antibody approved to treat multiple type 2 inflammatory conditions. Dupilumab-associated hypereosinophilia is a well-documented side effect and typically does not lead to clinical symptoms or pathologic findings. We report a 65-year-old man with asthma and nasal polyposis who presented with pleuritic chest pain after two doses of dupilumab. Our evaluation revealed peripheral hypereosinophilia and pericardial thickening consistent with pericarditis on cardiac MRI. The patient was treated with ibuprofen and colchicine, did not require corticosteroids, and dupilumab was discontinued. Subsequently, his eosinophil counts normalized, and his symptoms resolved. To our knowledge, this is the first published case of dupilumab-induced hypereosinophilia followed by isolated pericardial involvement.

Authors

Publication Details

Journal
Cureus
Published
2026-03-11
DOI
https://doi.org/10.7759/cureus.105073
Primary Topic
Eosinophilic Disorders and Syndromes
Type
article
Field-Weighted Citation Impact
0.00
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article

A Case of Acute Pericarditis and Hypereosinophilia After Dupilumab Initiation

Roy Artal, Sherwin R. Hariri, Marcel Hariri, Ani Shirvanian et al.
Cureus
Eosinophilic Disorders and Syndromes
article

A Case of Acute Pericarditis and Hypereosinophilia After Dupilumab Initiation

Roy Artal, Sherwin R. Hariri, Marcel Hariri, Ani Shirvanian, Tiffany Truong
article en

Abstract

Dupilumab is a monoclonal antibody approved to treat multiple type 2 inflammatory conditions. Dupilumab-associated hypereosinophilia is a well-documented side effect and typically does not lead to clinical symptoms or pathologic findings. We report a 65-year-old man with asthma and nasal polyposis who presented with pleuritic chest pain after two doses of dupilumab. Our evaluation revealed peripheral hypereosinophilia and pericardial thickening consistent with pericarditis on cardiac MRI. The patient was treated with ibuprofen and colchicine, did not require corticosteroids, and dupilumab was discontinued. Subsequently, his eosinophil counts normalized, and his symptoms resolved. To our knowledge, this is the first published case of dupilumab-induced hypereosinophilia followed by isolated pericardial involvement.

Cureus
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Eosinophilic Disorders and Syndromes
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