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嗜铬细胞瘤危象

Pheochromocytoma crisis.

作者信息

Newell K, Prinz R A, Braithwaite S, Brooks M

机构信息

Loyala University Medical Center, Department of Surgery and Medicine, Maywood, Illinois 60153.

出版信息

Am J Hypertens. 1988 Jul;1(3 Pt 3):189S-191S. doi: 10.1093/ajh/1.3.189s.

Abstract

Of 26 patients with pheochromocytoma treated between 1974 and 1986, two presented with pheochromocytoma crisis. This unusual presentation consists of hyper- and/or hypotension, high fevers (greater than 40 degrees C), encephalopathy, and multiple organ system failure. Both patients had large tumors associated with markedly elevated levels of epinephrine. Although hypertension was adequately controlled in both patients with phenoxybenzamine, phentolamine (1 patient) and nitroprusside, both patients deteriorated rapidly. The first patient expired during attempts to identify a source of sepsis. None was found at autopsy. The second patient underwent urgent adrenalectomy which reversed the multiple organ system failure and resulted in patient survival. We conclude from review of these patients and three others in the literature that (a) crisis is an unusual presentation of pheochromocytoma; (b) its manifestations include vascular lability, high fever, encephalopathy and multiple organ system failure; (c) it may be the result of increased epinephrine secretion; (d) successful treatment of pheochromocytoma crisis demands prompt diagnosis, vigorous medical therapy and emergent tumor removal if the patient continues to deteriorate.

摘要

在1974年至1986年间接受治疗的26例嗜铬细胞瘤患者中,有2例出现了嗜铬细胞瘤危象。这种不寻常的表现包括高血压和/或低血压、高热(超过40摄氏度)、脑病以及多器官系统衰竭。两名患者均有大肿瘤,且肾上腺素水平显著升高。尽管使用苯氧苄胺、酚妥拉明(1例患者)和硝普钠对两名患者的高血压进行了充分控制,但两名患者均迅速恶化。第一名患者在试图确定败血症来源的过程中死亡。尸检未发现任何问题。第二名患者接受了紧急肾上腺切除术,这逆转了多器官系统衰竭并使患者存活。通过对这些患者以及文献中的其他三名患者的回顾,我们得出以下结论:(a)危象是嗜铬细胞瘤的一种不寻常表现;(b)其表现包括血管不稳定、高热、脑病和多器官系统衰竭;(c)它可能是肾上腺素分泌增加的结果;(d)嗜铬细胞瘤危象的成功治疗需要及时诊断、积极的药物治疗以及如果患者持续恶化则紧急切除肿瘤。

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