硬皮病心脏病并发猝死1例心律失常的临床病理分析。

European journal of cardiology Pub Date : 1981-01-01
P G Marinato, G Thiene, L Menghetti, G F Buja, A Nava, A Cecchetto, L Rossi
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引用次数: 0

摘要

电生理和组织病理学的相关性已经进行了硬皮病心脏病患者,影响晕厥发作,谁死于记录心室颤动。电生理检查揭示了窦房传导功能障碍,表现为窦房传导阻滞和心房早搏后异常的返回周期模式。心房起搏时心房有效不应期和功能不应期增加,人工刺激与心房之间出现不寻常的“伪温克巴赫”现象。心房起搏100次/分时房室结传导时间正常上限,出现wenkebach型房室传导阻滞。左前半部分存在时,HV传导中度延长。这些电生理障碍的组织病理学基础是窦房结纤维化,结间通路和房室-房房结连接中断,左束支萎缩。就致死性心动过速而言,肌原纤维变性可能与其发病机制有关。提示普通心肌和特化传导系统的病变是硬皮病患者电不稳定的原因。
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Clinicopathologic assessment of arrhythmias in a case of scleroderma heart disease with sudden death.

Electrophysiologic and histopathologic correlation has been carried out in a patient with scleroderma heart disease, affected by syncopal seizures, who died of recorded ventricular fibrillation. The electrophysiological investigation disclosed dysfunction of sinoatrial conduction, revealed by sinoatrial blocks and by an abnormal return cycle pattern after premature atrial beats. Atrial effective and functional refractory periods were increased and an unusual 'pseudo-Wenckebach' phenomenon between artificial stimulus and atrium was observed during atrial pacing. Intra-AV nodal conduction time was at normal upper limits and Wenckebach-type AV block was obtained on pacing the atrium at 100 beats/min. HV conduction was moderately prolonged in the presence of left anterior hemiblock. The histopathologic substrates of these electrophysiologic disturbances were fibrosis of the sinus node, disrupted internodal pathways and atrio-AV nodal connections, and left bundle branch atrophy. As far as fatal tachyarrhythmia is concerned, myofibrillar degeneration may have contributed to its pathogenesis. It is suggested that both lesions of the ordinary myocardium and specialized conduction system account for the electrical instability of sclerodermic patients.

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