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复发性应激性心肌病:一名未确诊嗜铬细胞瘤的年轻患者中的罕见变体。

Recurrent Stress Cardiomyopathy: A Rare Variant in a Young Patient with Undiagnosed Pheochromocytoma.

作者信息

Lembo Robert, Wesley Paul, Calkins Joe B

机构信息

Department of Cardiovascular Medicine, Medical College of Georgia, 1120 15th Street, Augusta, GA 30912, USA.

出版信息

Case Rep Cardiol. 2021 Jun 1;2021:5518578. doi: 10.1155/2021/5518578. eCollection 2021.

Abstract

Biventricular stress cardiomyopathy is one of several known anatomical variants of reversible cardiomyopathies to occur. We present a case of a young patient with recurrent stress cardiomyopathy complicated by cardiogenic shock in the perioperative period. The cardiomyopathy observed was in a patient with neurofibromatosis type I and undiagnosed pheochromocytoma who presented for intervention of hydrocephalus. This case demonstrates the importance of vigilance in the young patient who develops shock in the perioperative period.

摘要

双心室应激性心肌病是几种已知的可逆性心肌病解剖学变异类型之一。我们报告一例年轻患者,其复发性应激性心肌病在围手术期并发心源性休克。观察到的心肌病发生在一名患有Ⅰ型神经纤维瘤病且未诊断出嗜铬细胞瘤的患者身上,该患者因脑积水接受干预治疗。该病例表明,对于在围手术期发生休克的年轻患者保持警惕非常重要。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/abdf/8195023/3710d2c489cc/CRIC2021-5518578.001.jpg

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