Newell K A, Prinz R A, Pickleman J, Braithwaite S, Brooks M, Karson T H, Glisson S
Department of Surgery, Loyola University, Maywood, Ill 60153.
Arch Surg. 1988 Aug;123(8):956-9. doi: 10.1001/archsurg.1988.01400320042007.
Three of 27 patients treated for pheochromocytoma between 1974 and 1987 presented with pheochromocytoma multisystem crisis (PMC). This unusual presentation consists of multiple organ system failure, temperature often greater than 40 degrees C, encephalopathy, and hypertension and/or hypotension. Although urgent medical therapy achieved blood pressure control in all three patients, the other manifestations of PMC progressed rapidly in spite of alpha and even beta blockade. The first patient died during attempts to localize a septic focus. The other two patients underwent urgent adrenalectomy and had postoperative improvement in their multiple organ system failure. All three tumors were large and produced markedly elevated levels of epinephrine. In conclusion (1) PMC is an unusual presentation of pheochromocytoma; (2) its manifestations include multiple organ system failure, high fever, encephalopathy, and vascular lability; (3) it may result from increased epinephrine secretion; and (4) successful treatment of PMC demands prompt diagnosis, vigorous medical preparation, and emergency tumor removal if the patient's condition continues to deteriorate.
1974年至1987年间接受嗜铬细胞瘤治疗的27例患者中有3例出现嗜铬细胞瘤多系统危象(PMC)。这种不寻常的表现包括多器官系统衰竭、体温常高于40摄氏度、脑病以及高血压和/或低血压。尽管紧急药物治疗使所有3例患者的血压得到控制,但尽管使用了α甚至β阻滞剂,PMC的其他表现仍迅速进展。首例患者在试图定位感染灶时死亡。另外两名患者接受了紧急肾上腺切除术,术后多器官系统衰竭有所改善。所有3个肿瘤都很大,肾上腺素水平显著升高。总之,(1)PMC是嗜铬细胞瘤的一种不寻常表现;(2)其表现包括多器官系统衰竭、高热、脑病和血管不稳定;(3)它可能由肾上腺素分泌增加引起;(4)成功治疗PMC需要及时诊断、积极的医疗准备,以及在患者病情持续恶化时紧急切除肿瘤。