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Cardiac Sarcoidosis Imitating Arrhythmogenic Right Ventricular Dysplasia
Author(s) -
Kibar Yared,
Amer M. Johri,
Anand Soni,
Matthew Johnson,
Tarik K. Alkasab,
Ricardo C. Cury,
Judy Hung,
Wilfred Mamuya
Publication year - 2008
Publication title -
circulation
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 7.795
H-Index - 607
eISSN - 1524-4539
pISSN - 0009-7322
DOI - 10.1161/circulationaha.107.755215
Subject(s) - medicine , arrhythmogenic right ventricular dysplasia , sarcoidosis , cardiology , cardiac sarcoidosis , dysplasia , cardiomyopathy , heart failure
A 59-year-old male was admitted to Massachusetts General Hospital, Boston, Mass, with a 2-month history of exertional dyspnea (New York Heart Association class II to III). The patient denied dyspnea at rest, chest pain, palpitations, or syncope. There was no history of fevers or recent weight loss.An outpatient echocardiogram (Figure 1), performed as part of the workup of the patient’s dyspnea, demonstrated normal left ventricular size and function. The right ventricle (RV) was normal in size but diffusely hypokinetic. There was evidence of segmental RV dysfunction, with 2 discrete aneurysmal areas in the RV free wall at the base and apex, which measured 1.5 and 3.0 cm in width. Both areas appeared thinned and dyskinetic. The echocardiographic appearance was suggestive of arrhythmogenic RV dysplasia/cardiomyopathy (ARVD/C).1 A CT scan ruled out the presence of pulmonary embolism but was notable for marked mediastinal lymphadenopathy (Figure 2 …

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