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Peer-reviewedCC BY 4.0Frontiers in Cardiovascular Medicine

Case Report: Upper septal fascicular ventricular tachycardia mimicking supraventricular tachycardia: diagnostic pitfalls and mapping-guided ablation

  1. 1School of Medicine, University of Electronic Science and Technology of China
  2. 2Department of Cardiology, Sichuan Provincial People’s Hospital, University of Electronic Science and Technology of China

Abstract

Background: Upper septal fascicular ventricular tachycardia (VT) is a rare form of idiopathic left ventricular tachycardia arising from the proximal His-Purkinje system. Because near-synchronous ventricular activation can produce a relatively narrow QRS complex, this arrhythmia may closely mimic supraventricular tachycardia (SVT) with aberrant conduction.

Case presentation: A 25-year-old man without structural heart disease presented with recurrent palpitations for more than 4 years. ECG during tachycardia showed a regular narrow-complex tachycardia at approximately 200 beats/min with atypical right bundle-branch block-like morphology and marked right-axis deviation. Electrophysiological study initially raised suspicion for an AVNRT-like mechanism because programmed atrial stimulation demonstrated dual AV nodal physiology and intracardiac recordings showed an apparent near-simultaneous ventriculoatrial relationship. However, 6 mg intravenous adenosine did not terminate the tachycardia but unmasked atrioventricular dissociation, with the ventricular rate exceeding the atrial rate; together with subsequent Purkinje-system mapping, this supported a ventricular origin. Initial mapping identified an effective target in the distal left posterior fascicular region, where 30-W radiofrequency ablation terminated the tachycardia. The same night, incessant tachycardia recurred with a changed and narrower QRS morphology. Repeat mapping localized the final successful target to the upper septal region approximately 8 mm from the His bundle; 20-W radiofrequency ablation terminated the tachycardia without atrioventricular conduction injury. No symptomatic recurrence was reported during 12-month clinical follow-up.

Conclusion: A relatively narrow or progressively narrowing QRS complex does not exclude VT. In suspected SVT with atypical features, adenosine-unmasked atrioventricular dissociation should prompt reconsideration of a ventricular mechanism, while invasive electrophysiological assessment and repeat mapping may facilitate accurate diagnosis and safe ablation, particularly when the arrhythmogenic substrate is adjacent to the His bundle.

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BibTeX
@article{fu2026case,
  title = {{Case Report: Upper septal fascicular ventricular tachycardia mimicking supraventricular tachycardia: diagnostic pitfalls and mapping-guided ablation}},
  author = {Yilin Fu and Jia Tang and Zixiang Zhao and Yongxiang Cai and Yang Chen},
  journal = {Frontiers in Cardiovascular Medicine},
  year = {2026},
  month = oct,
  doi = {10.3389/fcvm.2026.1933819},
  url = {https://www.frontiersin.org/articles/10.3389/fcvm.2026.1933819/full},
  note = {CC BY 4.0},
}
RIS
TY  - JOUR
TI  - Case Report: Upper septal fascicular ventricular tachycardia mimicking supraventricular tachycardia: diagnostic pitfalls and mapping-guided ablation
AU  - Yilin Fu
AU  - Jia Tang
AU  - Zixiang Zhao
AU  - Yongxiang Cai
AU  - Yang Chen
PY  - 2026
DA  - 2026/10/29
JO  - Frontiers in Cardiovascular Medicine
DO  - 10.3389/fcvm.2026.1933819
UR  - https://www.frontiersin.org/articles/10.3389/fcvm.2026.1933819/full
AB  - Background: Upper septal fascicular ventricular tachycardia (VT) is a rare form of idiopathic left ventricular tachycardia arising from the proximal His-Purkinje system. Because near-synchronous ventricular activation can produce a relatively narrow QRS complex, this arrhythmia may closely mimic supraventricular tachycardia (SVT) with aberrant conduction.  Case presentation: A 25-year-old man without structural heart disease presented with recurrent palpitations for more than 4 years. ECG during tachycardia showed a regular narrow-complex tachycardia at approximately 200 beats/min with atypical right bundle-branch block-like morphology and marked right-axis deviation. Electrophysiological study initially raised suspicion for an AVNRT-like mechanism because programmed atrial stimulation demonstrated dual AV nodal physiology and intracardiac recordings showed an apparent near-simultaneous ventriculoatrial relationship. However, 6 mg intravenous adenosine did not terminate the tachycardia but unmasked atrioventricular dissociation, with the ventricular rate exceeding the atrial rate; together with subsequent Purkinje-system mapping, this supported a ventricular origin. Initial mapping identified an effective target in the distal left posterior fascicular region, where 30-W radiofrequency ablation terminated the tachycardia. The same night, incessant tachycardia recurred with a changed and narrower QRS morphology. Repeat mapping localized the final successful target to the upper septal region approximately 8 mm from the His bundle; 20-W radiofrequency ablation terminated the tachycardia without atrioventricular conduction injury. No symptomatic recurrence was reported during 12-month clinical follow-up.  Conclusion: A relatively narrow or progressively narrowing QRS complex does not exclude VT. In suspected SVT with atypical features, adenosine-unmasked atrioventricular dissociation should prompt reconsideration of a ventricular mechanism, while invasive electrophysiological assessment and repeat mapping may facilitate accurate diagnosis and safe ablation, particularly when the arrhythmogenic substrate is adjacent to the His bundle.
SN  - 2297-055X
ER  -