Successful ablation of coexistent Mahaim tachycardia and right posterior accessory pathway in a patient with Ebstein's anomaly


Göl E. E., AKDENİZ C., TUZCU V.

Turk Kardiyoloji Dernegi Arsivi, vol.44, no.5, pp.423-426, 2016 (Scopus) identifier identifier identifier

  • Publication Type: Article / Review
  • Volume: 44 Issue: 5
  • Publication Date: 2016
  • Doi Number: 10.5543/tkda.2015.31624
  • Journal Name: Turk Kardiyoloji Dernegi Arsivi
  • Journal Indexes: Scopus, TR DİZİN (ULAKBİM)
  • Page Numbers: pp.423-426
  • Keywords: Accessory pathway, Ebstein's anomaly, Mahaim pathway
  • Istanbul Medipol University Affiliated: Yes

Abstract

The atriofascicular accessory pathway (AP), known as the Mahaim pathway, is a rare form of pre-excitation, comprising less than 3% of all APs. Mahaim AP is characterized by decremental, anterograde-only conduction, and antidromic tachycardia with left bundle branch morphology. Prevalence of Mahaim AP in Ebstein's anomaly is significantly high. In addition, combination of Wolff- Parkinson-White (WPW) syndrome and Mahaim AP in patients with Ebstein's anomaly has been reported. Presently described is the coexistence of Mahaim AP and manifest WPW syndrome in a patient with Ebstein's anomaly, who was successfully ablated without fluoroscopy.