Cardiovascular magnetic resonance in familial amyloidosis
نویسندگان
چکیده
منابع مشابه
Cardiovascular magnetic resonance in familial amyloidosis
Methods Our objective was to identify morphological and functional findings of familial amyloidosis in Cardiovascular Magnetic Resonance and compare this findings between asymptomatic patients and those with cardiovascular symptoms. Cardiovascular Magnetic Resonance was performed in 19 patients with familiar amyloidosis, 9 of them with cardiovascular symptoms, the remaining 10 were asymptomatic...
متن کاملCardiovascular Magnetic Resonance in Cardiac Amyloidosis
Background—Cardiac amyloidosis can be diagnostically challenging. Cardiovascular magnetic resonance (CMR) can assess abnormal myocardial interstitium. Methods and Results—Late gadolinium enhancement CMR was performed in 30 patients with cardiac amyloidosis. In 22 of these, myocardial gadolinium kinetics with T1 mapping was compared with that in 16 hypertensive controls. One patient had CMR and ...
متن کاملCardiovascular magnetic resonance in cardiac amyloidosis.
BACKGROUND Cardiac amyloidosis can be diagnostically challenging. Cardiovascular magnetic resonance (CMR) can assess abnormal myocardial interstitium. METHODS AND RESULTS Late gadolinium enhancement CMR was performed in 30 patients with cardiac amyloidosis. In 22 of these, myocardial gadolinium kinetics with T1 mapping was compared with that in 16 hypertensive controls. One patient had CMR an...
متن کاملCardiovascular Magnetic Resonance and prognosis in cardiac amyloidosis
BACKGROUND Cardiac involvement is common in amyloidosis and associated with a variably adverse outcome. We have previously shown that cardiovascular magnetic resonance (CMR) can assess deposition of amyloid protein in the myocardial interstitium. In this study we assessed the prognostic value of late gadolinium enhancement (LGE) and gadolinium kinetics in cardiac amyloidosis in a prospective lo...
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ژورنال
عنوان ژورنال: Journal of Cardiovascular Magnetic Resonance
سال: 2016
ISSN: 1532-429X
DOI: 10.1186/1532-429x-18-s1-p266