Myocarditis in systemic immune-mediated diseases: Prevalence, characteristics and prognosis. A systematic review

CY Cheng, A Baritussio, AS Giordani, S Iliceto… - Autoimmunity …, 2022 - Elsevier
Many systemic immune-mediated diseases (SIDs) may involve the heart and present as
myocarditis with different histopathological pictures, ie lymphocytic, eosinophilic …

Eosinophilic myocarditis: systematic review

W Techasatian, M Gozun, K Vo, J Yokoyama… - Heart, 2024 - heart.bmj.com
Objective In clinical practice, patients with eosinophilic myocarditis (EM) may forgo the gold
standard diagnostic procedure, endomyocardial biopsy (EMB), although it is highly …

MR and CT angiography in the diagnosis of vasculitides

A Ghorishi, A Alayon, T Ghaddar, M Kandah… - BJR| Open, 2023 - academic.oup.com
Vasculitides represent the wide-ranging series of complex inflammatory diseases that
involve inflammation of blood vessel walls. These conditions are characterized according to …

[HTML][HTML] Management of Coronary Artery Diseases in Systemic Vasculitides: Complications and Strategies

R Shumnalieva, N Mileva, I Padjen, P Siliogkas… - Medicina, 2024 - pmc.ncbi.nlm.nih.gov
Coronary artery disease (CAD) presents a significant risk for patients with systemic
vasculitides, a group of disorders characterized by the inflammation of blood vessels. In this …

The diagnostic challenge of eosinophilic granulomatosis with polyangiitis presenting as acute eosinophilic myocarditis: case report and literature review

H Yamamoto, K Hashimoto, Y Ikeda, J Isogai… - Frontiers in …, 2022 - frontiersin.org
Eosinophilic granulomatosis with polyangiitis (EGPA) is a systemic vasculitis involving small-
to-medium-sized vessels characterized by asthma, vasculitis, and peripheral eosinophilia …

Current evidence in the diagnosis and management of coronary arteritis presenting as acute coronary syndrome

Z Lin, L Jia, D Yin, W Song, H Wang, Q Dong… - Current Problems in …, 2023 - Elsevier
Acute coronary syndromes (ACS) are defined by a sudden reduction in blood supply to the
heart, and an estimated more than seven million people are diagnosed with ACS worldwide …

[HTML][HTML] The critical role of cardiac magnetic resonance imaging in evaluating patients with eosinophilic granulomatosis with polyangiitis

S Sridharan, S Nanthakumaran, MR Somagutta… - Cureus, 2020 - ncbi.nlm.nih.gov
Eosinophilic granulomatosis with polyangiitis (EGPA) is a rare autoimmune systemic
necrotizing vasculitis of blood vessels that often presents with hypereosinophilia. Cardiac …

[PDF][PDF] Myocardial Involvement in Systemic Autoimmune Rheumatic Diseases

AA Zagouras, WHW Tang - Rheumatic Disease Clinics of North America, 2023 - Elsevier
Systemic autoimmune diseases are defined by their potential to affect multiple organ
systems, and when treating patients with SARDs it is important to consider the possibility of …

[HTML][HTML] Endomyocardial biopsy facilitates diagnosis of eosinophilic granulomatosis with polyangiitis (EGPA): a case report

AB Wilhelm, S Pinsky, S Ahmad, A Cunningham… - Cardiovascular …, 2022 - Elsevier
Background Eosinophilic granulomatosis with polyangiitis (EGPA) is a rare small vessel
leukocytoclastic vasculitis that affects multiple organs and is often associated with anti …

Myopericarditis as a presentation of eosinophilic granulomatosus with polyangiitis (EGPA)

M Dey, J Nair, R Sankaranarayanan… - BMJ Case Reports …, 2019 - casereports.bmj.com
A 60-year-old woman was admitted to the hospital with worsening dyspnoea, cough and
chest pain. This was on a background of weight loss, decreased appetite, mononeuritis …