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Published on: February 17, 2018
Mahaim Tachycardia Induced Cardiomyopathy
Ibrahim Gul1, Qamaruddin Roziman1, Aamir Hameed Khan1
1Department of Medicine, Section of Cardiology, The Aga Khan University Hospital, Karachi.
This case report details a young man with palpitations and chest pain due to Mahaim tachycardia, a rare cause of cardiomyopathy. Successful radiofrequency ablation cured his condition, highlighting a treatable cause of heart dysfunction.
Area of Science:
- Cardiology
- Electrophysiology
- Cardiomyopathy
Background:
- Wide complex tachycardia (WCT) can present with various symptoms including palpitations, chest pain, and shortness of breath.
- Left ventricular (LV) systolic dysfunction, if severe, can lead to significant morbidity.
Observation:
- A 22-year-old male presented with 7 months of incessant palpitations, chest pain, shortness of breath, and neck pulsations.
- Previous echocardiography revealed severe LV systolic dysfunction and hypokinesia, which improved with medical therapy.
- Electrophysiological study identified a decremental right-sided atriofascicular pathway responsible for WCT with left bundle branch block (LBBB) morphology and left axis deviation (LAD), consistent with Mahaim tachycardia.
Findings:
- Mahaim tachycardia was diagnosed as the cause of the patient's symptoms and cardiomyopathy.
- Radiofrequency ablation (RF) successfully eliminated the atriofascicular pathway and the tachycardia.
Implications:
- This case highlights Mahaim tachycardia as a rare, yet curable, cause of tachycardia-induced cardiomyopathy.
- Successful ablation offers a definitive treatment option for patients with this specific type of WCT and associated cardiac dysfunction.
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