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Idiopathic Giant Cell Myocarditis
Annals of Pathology and Laboratory Medicine, 2018 Anita Neelkanth Kavatkar +2 more
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Herz, 2012
Giant cell myocarditis (GCM) usually presents as acute dilated cardiomyopathy that does not improve with guideline-based treatments. Ventricular tachycardia and heart block occur in a substantial number of patients. Diagnosis by endomyocardial biopsy can allow for the addition of immunosuppressive therapy and timely use of mechanical circulatory ...
L T, Cooper, C, ElAmm
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Giant cell myocarditis (GCM) usually presents as acute dilated cardiomyopathy that does not improve with guideline-based treatments. Ventricular tachycardia and heart block occur in a substantial number of patients. Diagnosis by endomyocardial biopsy can allow for the addition of immunosuppressive therapy and timely use of mechanical circulatory ...
L T, Cooper, C, ElAmm
openaire +3 more sources
The American Journal of Medicine, 1985
The present report describes a 45-year-old man with giant cell myocarditis who died of heart failure eight months after the onset of symptoms. On postmortem examination, the heart showed extensive myocardial fibrosis with numerous multinucleated giant cells.
M S, Wilson +4 more
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The present report describes a 45-year-old man with giant cell myocarditis who died of heart failure eight months after the onset of symptoms. On postmortem examination, the heart showed extensive myocardial fibrosis with numerous multinucleated giant cells.
M S, Wilson +4 more
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Idiopathic giant cell myocarditis
Current Treatment Options in Cardiovascular Medicine, 2001Idiopathic giant cell myocarditis (IGCM) is an uncommon disorder that is of general importance because it most commonly affects young individuals, is usually fatal without treatment, and may respond to aggressive medical and surgical therapy. IGCM is most often progressive over days to weeks and frequently requires the concurrent management of ...
Leslie T., Cooper, Yuji, Okura
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Asymptomatic giant cell granulomatous myocarditis
American Heart Journal, 1966Abstract A 76-year-old man who was known to be an epileptic died from a massive subdural hematoma and a rapidly progressive renal insufficiency. Incidental findings at necropsy were the histopathologic changes of giant cell granulomatous myocarditis and granulomatous nodules in the lungs.
W M, O'Donnell, R H, Mann
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Pathology, 2014
Context Giant cell myocarditis is a very rare disease difficult to diagnose with poor prognosis in its severe form. With this context we present the particularities of such a case investigated at Emergency Care Hospital in M Ciuc Romania. Material and method A 28-year-old female patient with respiratory syndrome, died suddenly with myocardial ...
Valentin Tiberiu Moldovan +2 more
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Context Giant cell myocarditis is a very rare disease difficult to diagnose with poor prognosis in its severe form. With this context we present the particularities of such a case investigated at Emergency Care Hospital in M Ciuc Romania. Material and method A 28-year-old female patient with respiratory syndrome, died suddenly with myocardial ...
Valentin Tiberiu Moldovan +2 more
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The Journal of heart and lung transplantation : the official publication of the International Society for Heart Transplantation, 1995
Giant cell myocarditis is a rare and frequently fatal disorder of unknown origin that is defined histopathologically as diffuse myocardial necrosis with multinucleated giant cells in the absence of sarcoidlike granulomata. The clinical and pathologic features of lymphocytic myocarditis have been described in several recent publications, but the ...
L T, Cooper +3 more
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Giant cell myocarditis is a rare and frequently fatal disorder of unknown origin that is defined histopathologically as diffuse myocardial necrosis with multinucleated giant cells in the absence of sarcoidlike granulomata. The clinical and pathologic features of lymphocytic myocarditis have been described in several recent publications, but the ...
L T, Cooper +3 more
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Giant Cell and Granulomatous Myocarditis
Heart Failure Clinics, 2005Although myocarditis first was described in 1837, the distinction between histologic subtypes did not occur until the late 19th century. In 1905, Saltykow [1] described a case of fatal myocarditis characterized by giant cells associated with a widespread inflammatory infiltrate and myocyte destruction.
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