EGPA presenting as sudden cardiac arrest: a case report and review of cardiac manifestations

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Authors: h. zhang, Miaolin Zhang, Tao Yu, Zhi Zhang, Mengyang Cai, Gang Wang, Weizong Zhang, Huamin Yu, Hong Yuan
Cited by: 1
References: 14

Abstract

Eosinophilic granulomatosis with polyangiitis (EGPA) is a rare systemic vasculitis in which cardiac involvement is a primary cause of mortality. Complete heart block presenting as Adams-Stokes syndrome is a rare but critical complication. Notably, to our knowledge, EGPA initially manifesting as Adams-Stokes syndrome has not been previously documented, based on a comprehensive review of the literature. We report a 27-year-old female presenting with recurrent syncope and seizures. Laboratory tests revealed significant eosinophilia (49.5%), and cardiac workup confirmed third-degree atrioventricular block. A diagnosis of EGPA was established based on the 2022 ACR/EULAR criteria (score=13). Emergency treatment involved temporary pacing and methylprednisolone pulse therapy, followed by mepolizumab induction. Sinus rhythm recovered within 24 hours. During a two-month follow-up, the patient maintained remission with normalized eosinophil counts and improved cardiac function. This case highlights the importance of including EGPA in the differential diagnosis of unexplained high-grade heart block and supports the efficacy of early immunosuppressive therapy in reversing life-threatening cardiac complications.

Fields of Study & Subjects

Vasculitis and related conditions Eosinophilic Disorders and Syndromes Pericarditis and Cardiac Tamponade

Publication details

Journal / source
Frontiers in Immunology
Publisher
Frontiers Media SA
Volume
16
Pages
1749843–1749843
Publication date
15 January 2026
Language
EN