| Literature DB >> 22248870 |
Omar Wever-Pinzon1, Jorge Romero, Juan P Cordova.
Abstract
Japanese-variant or apical hypertrophic cardiomyopathy (HCM) is a specific type of HCM, first described in Japan and initially thought to carry a benign prognosis. However, current evidence suggests that these patients experience severe symptoms and are at increased risk of ventricular arrhythmias and death, especially in the presence of an apical akinetic chamber. The management of patients who do not respond to medical therapy is challenging. We describe a patient with Japanese-variant HCM, with an apical akinetic chamber and severe symptoms who failed medical therapy. The use of dual chamber pacing relieved obstruction and significantly improved the patient's symptoms.Entities:
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Year: 2013 PMID: 22248870 PMCID: PMC3672355 DOI: 10.1097/MJT.0b013e31821109ff
Source DB: PubMed Journal: Am J Ther ISSN: 1075-2765 Impact factor: 2.688