Cardiac Sarcoid: A Chameleon Masquerading as Hypertrophic Cardiomyopathy and Dilated Cardiomyopathy in the Same Patient. Issue 5 (8th February 2014)

• Record Type: Journal Article
• Authors: Agarwal, Anushree; Sulemanjee, Nasir Z.; Cheema, Omar; Downey, Francis X.; Tajik, A. Jamil
• Is Part Of: Echocardiography. Volume 31:Issue 5(2014)
• Page Start: E138
• Page End: E141
• Publication Date: 2014-02-08
• Subjects: Echocardiography -- Periodicals; Echocardiography -- Periodicals; 616.1207543
• DOI: 10.1111/echo.12536
• Languages: English
• ISSNs: 0742-2822

Abstract

<abstract abstract-type="main" id="echo12536-abs-0003"> <title> <x xml:space="preserve">Abstract</x> </title> <p>Sarcoidosis is a multisystem, granulomatous disease of unknown etiology often seen in young adults, with cardiac involvement in more than one‐quarter of sarcoid patients. The clinical presentation of cardiac sarcoid depends upon the location and extent of myocardium involved. Although cardiac sarcoid may produce asymmetrical septal hypertrophy, it is most commonly considered in the differential diagnosis of dilated cardiomyopathy. The hypertrophic stage of cardiac sarcoid is rarely seen. We describe a case of cardiac sarcoid in a young patient wherein a distinctive appearance of the cardiac sarcoid spectrum from "hypertrophic" stage to thinned/scarred stage, masquerading as hypertrophic cardiomyopathy followed by dilated cardiomyopathy, is demonstrated.</p> </abstract>