Evidence map›Paper›PMID 42080450›Full record

ArticleEuropean journal of rheumatology2026

Unmasking Eosinophilic Granulomatosis with Polyangiitis: A Case of Rapid-Onset Myositis Following COVID-19 Booster in an Eosinophilic Asthma Patient.

Anisha Memdani, Vishal Busa, Samhitha Avula, Alexis Ford, Joseph Nesheiwat

Abstract read
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Article in European journal of 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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0citing papers in PubMed
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1 · What the graph read from it

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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.

2 · The registry

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

5 authors.

Anisha MemdaniBaton Rouge General Medical Center, Louisiana, United States.
Vishal BusaDepartment of Internal Medicine, SUNY Upstate Medical University, New York, United States.
Samhitha AvulaBaton Rouge General Medical Center, Louisiana, United States.
Alexis FordBaton Rouge General Medical Center, Louisiana, United States.
Joseph NesheiwatBaton Rouge Clinic, Louisiana, United States.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Eosinophilic Granulomatosis with Polyangiitis (EGPA) is a rare Anti-neutrophil cytoplasm antibodies (ANCA)-associated vasculitis with multi-organ involvement and eosinophilia. We present a 61-year-old male with a history of eosinophilic asthma who developed progressive weakness and muscle aches six weeks after his second COVID-19 booster. Four to six weeks post vaccination, he developed myal gias and weakness, especially in proximal muscles, leading to a severe decline in function. Lab results showed leukocytosis (29.54 cells/mm³); 54% eosinophils; and elevated erythrocyte sedimentation rate (ESR), C-reactive protein, and creatine kinase levels at 13 736 u/L. Anti-myeloperoxidase antibodies were positive, while PR-3, C-ANCA, and P-ANCA were negative. Magnetic resonance imaging of the lower extremities showed intramuscular edema. Muscle biopsies confirmed EGPA. Diagnosed per American College of Rheumatology (ACR)/ European Alliance of Associations for Rheumatology (EULAR) criteria, he received pulse dose IV methylprednisolone with significant improvement. He was discharged on 60 mg prednisone and started on mepolizumab (300 mg subcutaneous once every 4 weeks). Eosinophilic granulomatosis with polyangiitis progresses through stages: asthma, eosinophilia with organ involvement, and vasculitis. This case highlights a unique presentation of rapid myositis without significant involvement of any other organs and vasculitis post-mRNA vaccination. While environmental factors may trigger EGPA, the role of COVID-19 vaccines remains hypothesis-generating. This case underscores the importance of post-market surveillance for rare events, contributing to the understanding of vaccine-related rheumatic disease triggers Cite this article as: Memdani A, Busa V, Avula S, Ford A, Nesheiwat J. Unmasking Eosinophilic granulomatosis with polyangiitis: a case of rapid-onset myositis following COVID-19 booster in an eosinophilic asthma patient. Eur J Rheumatol. 2025, 13(1), 0016, doi:10.5152/eurjrheum.2026.25016.

Identifiers

PMID42080450
PMCPMC13083772

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