永久性起搏器植入治疗全垂体功能低下患者继发于急性胰腺炎的房室传导阻滞。

Jacopo Giovacchini, Silvia Menale, Irene Merilli, Valentina Scheggi
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引用次数: 0

摘要

背景:垂体功能低下可能通过多种机制引发急性胰腺炎(AP)的发展。AP可改变正常的心内传导,导致房室传导阻滞。由于缺乏类似的病例,在这种情况下植入起搏器的正确时机和指征尚不清楚。病例介绍:一名22岁女性,在替代治疗中行额叶星形细胞瘤次全切除并残留垂体功能减退症,因AP和胰周坏死,并发低血压,窦性心动过缓伴2:1房室传导阻滞,严重急性呼吸窘迫综合征,需要插管和机械通气而入住急诊科。在住院期间,患者出现全身炎症反应综合征和急性肾衰竭,静脉注射多巴胺、利尿剂和液体治疗。虽然她逐渐恢复,但AP消退后仍持续存在晚期房室传导阻滞;因此,植入了一个永久性起搏器。在随访期间,检测到适当的设备干预。结论:文献中未见其他高级别房室传导阻滞的报道。本病例提示,如果房室传导阻滞不随AP消退而恢复,则必须使用起搏器。需要进一步的证据来改善垂体功能低下患者并发AP的节律障碍管理。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Permanent pacemaker implantation for atrioventricular block secondary to acute pancreatitis in a patient affected by panhypopituitarism.

Background: Hypopituitarism may trigger the development of acute pancreatitis (AP) through multiple mechanisms. AP may alter normal intracardiac conduction leading to an atrioventricular block. Due to the lack of similar cases, the correct timing and indication for pacemaker implantation in such a setting are unknown.

Case presentation: A 22-year-old woman with a history of sub-total excision of frontal astrocytoma with residual panhypopituitarism in replacement therapy was admitted to the emergency department with AP and peripancreatic necrosis, complicated by hypotension, sinus bradycardia with 2:1 atrioventricular block, and severe acute respiratory distress syndrome deserving intubation and mechanical ventilation. During the in-hospital course, the patient developed a systemic inflammatory response syndrome and acute kidney failure and was treated with intravenous dopamine, diuretics, and liquids. While she gradually recovered, advanced atrioventricular block persisted after the resolution of AP; therefore, a permanent pacemaker was implanted. During the follow-up, appropriate device interventions were detected.

Conclusions: No other cases of high-grade atrioventricular block in panhypopituitarism-induced AP have been reported in the literature. Our case suggests a pacemaker is necessary if the atrioventricular block does not recover with AP resolution. Further evidence is required to improve the management of rhythm disturbances in hypopituitarism patients who develop AP.

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