[AL-amyloidosis with cardiac involvement. Diagnostic capabilities of non-invasive methods]
A Y Gudkova1,2, S V Lapekin1, T G Bezhanishvili1
1Pavlov First Saint Petersburg State Medical University.
Abstract:
There are presented the literature data and a description of the clinical course of the disease in isolated/predominant cardiac amyloidosis. Amyloid cardiomyopathy is the most common phenocopy of hypertrophic cardiomyopathy. The modern possibilities of non-invasive diagnostics using osteoscintigraphy for the differential diagnosis between amyloid cardiomyopathy caused by AL- and transthyretin amyloidosis are described in detail.
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