Towards a Diagnosis of Cardiac Amyloidosis: Single Center Experience with ^99m Technetium Pyrophosphate Planar Imaging and Opportunities for Standardization of Diagnostic Workflow

<i>Background and Objectives</i>: Cardiac amyloidosis is a disorder caused by amyloid fibril deposition in the extracellular space of the heart. Almost all forms of clinical cardiac amyloidosis are transthyretin amyloidosis (ATTR) or light chain amyloidosis. ^99m technetium pyrophosphate (...

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Bibliografski detalji

Glavni autori:	Mariam Saleem, Besher Sadat, Meredith Van Harn, Karthikeyan Ananthasubramaniam
Format:	Artigo
Jezik:	Inglês
Izdano:	MDPI AG 2023-02-01
Serija:	Medicina
Teme:	cardiac amyloidosis transthyretin cardiac amyloidosis light chain amyloidosis technetium pyrophosphate scan restrictive cardiomyopathy
Online pristup:	https://www.mdpi.com/1648-9144/59/2/378
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