Mantovan R, Viani S, Stritoni P
Divisione di Cardiologia, Ospedale Regionale di Treviso.
G Ital Cardiol. 1999 Mar;29(3):315-20.
Permanent junctional reentrant tachycardia (PJRT) is an uncommon form of tachycardia that is usually due to an atrioventricular reentry via a right posteroseptal accessory pathway with decremental properties. We describe a case of PJRT that showed evidence of two accessory pathways located both left and right. A 63-year-old woman was referred to our institution for radiofrequency (RF) ablation of a permanent form of regular narrow QRS tachycardia (T) (cycle length 520 ms) with long RP interval (380 ms); P wave was negative in inferior leads, negative in D1 and flat in aVL. During sinus rhythm, AH and HV intervals were 110 ms and 50 ms respectively. The atrioventricular anterograde conduction curve was continuous. A decremental retrograde conduction via a left posterior pathway until ventricular effective refractory period (210 ms) was evident. Tachycardia inducible with both atrial and ventricular programmed stimulation was almost incessant. During tachycardia, a premature ventricular depolarization delivered when His bundle was refractory was able to advance the next atriogram, and tachycardia could be interrupted by a ventricular depolarization without atrial capture. During right atrial mapping, an earliest atrial activation was found in the mid-septal position just above the coronary sinus ostium and RF application caused a transient interruption of T (3 minutes). Tachycardia resumed with basal characteristics, but no evidence of earlier right atrial activation was found during atrial mapping. Successful RF ablation was performed via retrograde aortic catheterization in the left posterior region. This case showed evidence of a left posterior pathway causing PJRT. However, the transient successful ablation in the right mid-septal region and the lack of evidence of right early atrial activation after RF application could account for the presence of an additional right accessory pathway or a strand of the same broad left pathway.
永久性交界性折返性心动过速(PJRT)是一种不常见的心动过速形式,通常是由于经具有递减传导特性的右后间隔旁路进行房室折返所致。我们描述了一例PJRT病例,该病例显示存在位于左侧和右侧的两条旁路。一名63岁女性因射频(RF)消融一种永久性的规则窄QRS心动过速(T)(周长520毫秒)伴长RP间期(380毫秒)而转诊至我院;下壁导联P波为负,D1导联P波为负,aVL导联P波平坦。在窦性心律时,AH间期和HV间期分别为110毫秒和50毫秒。房室前传传导曲线是连续的。经左后旁路的递减性逆向传导直至心室有效不应期(210毫秒)很明显。心房和心室程控刺激均可诱发的心动过速几乎是持续性的。在心动过速期间,当希氏束不应期时发放的室性早搏能够提前下一次心房电图,并且心动过速可被无心房夺获的室性激动中断。在右心房标测时,最早的心房激动位于冠状窦口上方的中隔位置,射频消融导致心动过速短暂中断(3分钟)。心动过速恢复至基础特征,但在心房标测期间未发现更早的右心房激动证据。通过逆行主动脉导管在左后区域成功进行了射频消融。该病例显示存在导致PJRT的左后旁路证据。然而,右中隔区域的短暂成功消融以及射频消融后缺乏右心房早期激动证据可能解释了存在额外的右旁路或同一宽阔左旁路的分支。