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嗜铬细胞瘤性心原性休克。

Pheochromocytoma-induced cardiogenic shock.

机构信息

Department of Abdominal Surgery, Grand Hôpital de Charleroi, Gilly, Belgium.

Department of Anesthesiology, Grand Hôpital de Charleroi, Gilly, Belgium.

出版信息

Acta Chir Belg. 2023 Oct;123(5):573-576. doi: 10.1080/00015458.2022.2079822. Epub 2022 May 22.

Abstract

BACKGROUND

Pheochromocytoma is a rare catecholamine-secreting tumor of neuroendocrine origin. It has a prevalence of <1% in adults with hypertension. In some cases, hypertension is associated with the classical triad of headache, sweating, and tachycardia. Cardiogenic shock due to stress-induced cardiomyopathy caused by catecholamine excess may rarely be the initial symptom of pheochromocytoma, mimicking Takotsubo Syndrome.

METHODS

We report the case of a 58-year-old female patient with pheochromocytoma-induced cardiogenic shock (PICS) in the early postoperative period after thyroidectomy.

RESULTS

PICS is caused by a catecholamine storm, which induces myocardial stress and cardiac dysfunction. In such cases, early management with mechanical circulatory assistance may be promptly considered, given the increased risk of mortality.

CONCLUSION

PICS is a rare and serious condition. Prompt diagnosis and adequate resuscitation measures are necessary to avoid high mortality.

摘要

背景

嗜铬细胞瘤是一种罕见的神经内分泌来源的儿茶酚胺分泌肿瘤。它在高血压成人中的患病率<1%。在某些情况下,高血压与头痛、出汗和心动过速的经典三联征有关。由于儿茶酚胺过多引起的应激性心肌病导致的心源性休克可能很少是嗜铬细胞瘤的初始症状,类似于 Takotsubo 综合征。

方法

我们报告了一例 58 岁女性甲状腺切除术后早期发生的嗜铬细胞瘤诱导的心源性休克(PICS)病例。

结果

PICS 是由儿茶酚胺风暴引起的,它会导致心肌应激和心功能障碍。在这种情况下,由于死亡率增加,可能会及时考虑早期使用机械循环辅助治疗。

结论

PICS 是一种罕见且严重的疾病。及时诊断和充分的复苏措施是避免高死亡率所必需的。

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