Almatrafi Samah A, Quqandi Salma M, Ismail Samaher J, Alghamdi Khalid A
Internal Medicine, King Abdulaziz Medical City, Ministry of National Guard-Health Affairs, Jeddah, SAU.
Internal Medicine, King Abdullah International Medical Research Center, Jeddah, SAU.
Cureus. 2025 Jul 17;17(7):e88155. doi: 10.7759/cureus.88155. eCollection 2025 Jul.
Eosinophilic granulomatosis with polyangiitis (EGPA) is a form of multisystemic necrotizing vasculitis that has various manifestations. Cardiac involvement is one of the indications of poor prognosis, occurring with different reported prevalence. Due to the heterogeneity of EGPA presentation, its diagnosis relies on clinical condition supported by different investigations and classification criteria. However, large hemorrhagic pericardial effusion is a rare occurrence in EGPA, raising a diagnostic challenge with a wide differential diagnosis. EGPA can also affect other layers of the heart, making its development to perimyocarditis a warning for the progressive nature of the disease. We report a case of EGPA in a young female patient who presented initially with large hemorrhagic pericardial effusion, and later developed perimyocarditis.
嗜酸性肉芽肿性多血管炎(EGPA)是一种具有多种表现形式的多系统坏死性血管炎。心脏受累是预后不良的指标之一,其发生率报道不一。由于EGPA表现的异质性,其诊断依赖于不同检查和分类标准所支持的临床状况。然而,大量出血性心包积液在EGPA中较为罕见,这带来了诊断挑战,鉴别诊断范围广泛。EGPA还可影响心脏的其他层面,其发展为心肌外层炎提示疾病具有进展性。我们报告一例年轻女性EGPA患者,该患者最初表现为大量出血性心包积液,随后发展为心肌外层炎。