In this chapter, we will classify and describe cardiomyopathies according to their morphofunctional phenotype, providing information about their etiology and physiopathology. We will highlight the role of pathology and genetics in the diagnostic flowchart, providing input on the utility of the cardiac biopsy for specific disease. We will provide guidance for tissue triage and standards of morphologic evaluation, focusing on diagnostic clues that may allow the identification of the underlying etiology.

Cardiomyopathies / D'Amati, G.; Giordano, C.. - (2022), pp. 577-631. [10.1016/B978-0-12-822224-9.00014-1].

Cardiomyopathies

D'Amati G.
Primo
;
2022

Abstract

In this chapter, we will classify and describe cardiomyopathies according to their morphofunctional phenotype, providing information about their etiology and physiopathology. We will highlight the role of pathology and genetics in the diagnostic flowchart, providing input on the utility of the cardiac biopsy for specific disease. We will provide guidance for tissue triage and standards of morphologic evaluation, focusing on diagnostic clues that may allow the identification of the underlying etiology.
2022
Cardiovascular Pathology (Fifth Edition)
9780128222249
arrhythmogenic cardiomyopathy; dilated cardiomyopathy; histiocytoid cardiomyopathy; hypertrophic cardiomyopathy; left ventricular noncompaction; restrictive cardiomyopathy; stress cardiomyopathy; takotsubo disease
02 Pubblicazione su volume::02a Capitolo o Articolo
Cardiomyopathies / D'Amati, G.; Giordano, C.. - (2022), pp. 577-631. [10.1016/B978-0-12-822224-9.00014-1].
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11573/1677552
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