Case Report: Four cases of cardiac sarcoidosis in patients with inherited cardiomyopathy—a phenotypic overlap, co-existence of two rare cardiomyopathies or a second-hit disease

Case Report: Four cases of cardiac sarcoidosis in patients with inherited cardiomyopathy—a phenotypic overlap, co-existence of two rare cardiomyopathies or a second-hit disease

Cardiac sarcoidosis (CS), a rare condition characterized by non-caseating granulomas, can manifest with symptoms such as atrioventricular block and ventricular tachycardia (VT), as well as mimic inherited cardiomyopathies. A 48-year-old male presented with recurrent VT. The initial 18F-fluorodeoxygl...

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Hlavní autoři: Hans Ebbinghaus, Laura Ueberham, Daniela Husser-Bollmann, Andreas Bollmann, Ingo Paetsch, Cosima Jahnke, Ulrich Laufs, Borislav Dinov
Médium: Článek
Jazyk:English
Vydáno: Frontiers Media S.A. 2023-12-01
Edice:Frontiers in Cardiovascular Medicine
Témata:
cardiac sarcoidosis
non-ischemic cardiomyopathy
familial cardiomyopathy
ventricular tachyarrhythmias
conduction disease
On-line přístup:https://www.frontiersin.org/articles/10.3389/fcvm.2023.1328802/full

Internet

https://www.frontiersin.org/articles/10.3389/fcvm.2023.1328802/full

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