"Non parasitic hypereosinophilia revealing biventricular endomyocardial fibrosis" [PDF]
The Pan African Medical Journal, 2018 We report a case of a 7-year-old boy, without medical history, who presented a low weight-to-height ratio associated with effort dyspnea class III and hepatalgia.
Abdelkader Jalil El Hangouche +1 more
doaj +2 more sources
Biventricular Endomyocardial Fibrosis in a Patient With Chronic Myeloid Leukemia-Classical Imaging Diagnosis Not to Be Missed. [PDF]
CASE (Phila)Shams P, Tipoo Sultan FA.
europepmc +3 more sources
Complex right atrial mass in endomyocardial fibrosis: a diagnostic dilemma. [PDF]
BMJ Case Rep, 2019 Sharma A, Pandey NN, Malhi AS, Kumar S.
europepmc +3 more sources
The sad tale of a youthful right ventricle struggling with endomyocardial fibrosis. [PDF]
Oxf Med Case ReportsEl-Mhadi S +5 more
europepmc +3 more sources
Loeffler endomyocardial fibrosis [PDF]
European Heart Journal, 2006 A 58-year-old patient known for an idiopathic hyper-eosinophilic syndrome, previously treated with interferon, presented with severe dyspnoea and clinical signs of right ventricular (RV) failure. The transthoracic echocardiography (TTE) confirmed the RV systolic dysfunction with severe tricuspid valve (TV) regurgitation and an apical fibrotic ...
Bonvini, Robert +2 more
openaire +3 more sources
Endomyocardial fibrosis: A form of endemic restrictive cardiomyopathy [PDF]
Global Cardiology Science & Practice, 2012 Endomyocardial fibrosis is a form of endemic restrictive cardiomyopathy that affects mainly children and adolescents, and is geographically restricted to some poor areas of Africa, Latin America and Asia.
Ana Olga Mocumbi
doaj +1 more source
Endomyocardial fibrosis: still a mystery after 60 years.
PLoS Neglected Tropical Diseases, 2008 The pathologist Jack N. P. Davies identified endomyocardial fibrosis in Uganda in 1947. Since that time, reports of this restrictive cardiomyopathy have come from other parts of tropical Africa, South Asia, and South America.
Gene Bukhman, John Ziegler, Eldryd Parry
doaj +1 more source
A giant mystery in giant cell myocarditis: navigating diagnosis, immunosuppression, and mechanical circulatory support. [PDF]
, 2020 Giant cell myocarditis is a rare but often devastating diagnosis. Advances in cardiac imaging and mechanical circulatory support have led to earlier and more frequent diagnoses and successful management. This disease state has wide variation in acuity of
Dunn, Steven P +3 more
core +1 more source
A rare case report of hypertrophic cardiomyopathy induced by catecholamine-producing tumor [PDF]
, 2018 RATIONALE: Catecholamine-producing tumors are rare, occurring in less than 0.2% of patients with hypertension, but can have relevant cardiovascular morbidity and mortality. PATIENT CONCERNS: A 37-year-old woman presented with a history of dyspnea, chest
Bisogni, Valeria +12 more
core +1 more source