Eosinophilic granulomatosis with polyangitis presenting as Acute Coronary Syndrome
نویسندگان
چکیده
منابع مشابه
Eosinophilic Granulomatosis with Polyangitis Presenting as Cardiac Tamponade.
Eosinophilic granulomatosis with polyangitis (EGPA; earlier called Churg-Strauss syndrome) is a small-vessel necrotising vasculitis typically characterised by asthma, lung infiltrates, extra-vascular necrotising granulomas and hyper-eosinophilia. Cardiac disease is a major contributor to disease-related deaths in EGPA. We describe the case of a 39-year-old woman with late onset asthma, allergic...
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Eosinophilic myocarditis (EM) is a rare condition that may result from several heterogeneous eosinophilic diseases, including parasite infection, hypersensitivity reaction, vasculitis, and hypereosinophilic syndrome. Regardless of etiology, the disease may present with various cardiac conditions, such as acute coronary syndrome, heart failure, or arrhythmia. Irreversible endomyocardial fibrosis...
متن کاملEosinophilic Granulomatosis with Polyangiitis (Churg-Strauss Syndrome) Presenting as Diffuse
Marc-Etienne Parent, MD (Corresponding Author) 5 Résident, Département de Médecine Interne, Université de Sherbrooke 6 3001 12 Avenue, Fleurimont, QC, Canada J1H 5N4 7 Tel : 1-506-229-2155 8 Email : [email protected] 9 10 Benjamin Ellezam, MD, PhD, FRCPC 11 Professeur adjoint de clinique, Pathologie et biologie cellulaire, Université de Montréal 12 Directeur, Programme de résid...
متن کاملEosinophilic Granulomatosis with Polyangiitis Presenting as Acute Polyneuropathy Mimicking Guillain-Barre Syndrome
Eosinophilic granulomatosis with polyangiitis (EGPA) is a small-vessel vasculitis associated with antineutrophil cytoplasmic antibodies (ANCAs) which commonly affects the peripheral nervous system. A 38-year-old female with a history of asthma presented with a 2-week history of bilateral lower extremity paresthesias that progressed to symmetric ascending paralysis. Nerve conduction studies coul...
متن کاملGranulomatosis with polyangitis presenting with multiple cranial nerve palsies
Case presentation We report the case of localised granulomatosis with polyangitis in a 27 year old Caucasian gentleman who presented with multiple cranial neuropathies. He reported diplopia, hearing loss, dysphagia and dysarthria due to involvement of VI, XIII, IX, X and XII cranial nerves. A cerebral MRI demonstrated pachymeningitis along with mastoid changes and additional diagnostic workup s...
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ژورنال
عنوان ژورنال: Heart, Lung and Circulation
سال: 2015
ISSN: 1443-9506
DOI: 10.1016/j.hlc.2015.06.079