Cardiac involvements in hypereosinophilia‐associated syndrome: case reports and a little review of the literature

X Jin, C Ma, S Liu, Z Guan, Y Wang… - Echocardiography, 2017 - Wiley Online Library
Hypereosinophilia‐associated syndrome is a rare group of systemic diseases without
certain underlying causes. Hypereosinophilic syndrome (HES) and eosinophilic …

[HTML][HTML] Cardiac involvement in eosinophilic granulomatosis with polyangiitis: a meta-analysis of 62 case reports

M Pakbaz, M Pakbaz - The Journal of Tehran University Heart …, 2020 - ncbi.nlm.nih.gov
Background: Eosinophilic granulomatosis with polyangiitis (EGPA) is a rare multi-systemic
vasculitis, with cardiac involvement being one of its most serious manifestations. We aimed …

[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 …

Clinical features of myocardial infarction and myocarditis in young adults: a retrospective study

C Pellaton, P Monney, AJ Ludman, J Schwitter… - BMJ open, 2012 - bmjopen.bmj.com
Objectives To evaluate the prevalence and clinical presentation of myocardial infarction (MI)
and myocarditis in young adults presenting with chest pain (CP) and an elevated serum …

[HTML][HTML] Novel therapeutic options in inflammatory cardiomyopathy

G Kania, P Blyszczuk, B Müller-Edenborn… - Swiss Medical …, 2013 - smw.ch
Inflammatory dilated cardiomyopathy (iDCM) denotes cardiac dysfunction due to myocardial
inflammation (myocarditis). Progressively impaired cardiac contractility, fibrosis and dilation …

[PDF][PDF] Cardiac involvement in eosinophilic granulomatosis with polyangitis (Churg Strauss)(RCD code: I-3A. 7a)

W Szczeklik, T Miszalski-Jamka - J Rare Cardiovasc Dis, 2013 - scholar.archive.org
Eosinophilic granulomatosis with polyangitis–EGPA (previously known as Churg‑Strauss
syndrome) is a rare, systemic, necrotizing small‑vessel vasculitis with accompanying …

Eosinophilic myocarditis due to Churg–Strauss syndrome mimicking reversible dilated cardiomyopathy

M Chen, B Yu, D Peng, S Zhou - Heart & Lung, 2014 - Elsevier
A 41-year-old woman with a history of asthma arrived at the emergency room of our hospital
with dyspnea. The electrocardiogram showed no specific results. Echocardiography defects …

Anaesthetic management of a patient with eosinophilic granulomatosis with polyangiitis for internal fixation of a fractured femur

H Mohamed, ECEÓ Mathúna… - … Case Reports CP, 2021 - casereports.bmj.com
Eosinophilic granulomatosis with polyangiitis (EGPA) is a rare disease with an estimated
annual incidence of 0.5–6.8 per million. It is characterised by necrotising vasculitis with …

Cardiac manifestations in antineutrophil cytoplasmic autoantibody (ANCA)—associated vasculitides

K Życińska, A Borowiec - Polish Heart Journal (Kardiologia …, 2016 - journals.viamedica.pl
Anna Borowiec, MD, PhD graduated from the Medical University of Warsaw and is board
certified in internal medicine and cardiology. She is currently employed in the …

Cardiogenic Shock: An Unusual Initial Presentation of Churg‐Strauss Syndrome

M Apirami, JA Pratheepan, T Kumanan… - Case Reports in …, 2018 - Wiley Online Library
Churg‐Strauss syndrome (CSS) is a rare autoimmune condition, characterized by
necrotizing extravascular eosinophil rich granulomatous inflammation of the tissues and …