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[多灶性嗜铬细胞瘤的术中诊断]

[Intraoperative diagnosis of a multilocal pheochromocytoma].

作者信息

Egelhof J, Fürst H, Engelhardt D, Welte M

机构信息

Institut für Anästhesiologie, Klinikum Grosshadern, Ludwig-Maximilians-Universität Munchen.

出版信息

Anaesthesist. 1997 Sep;46(9):783-6. doi: 10.1007/s001010050469.

Abstract

Pheochromocytomas are functionally active, catecholamine-secreting tumours of chromaffin tissue. The mainstay of pharmacological therapy is preoperative treatment with oral phenoxybenzamine. This drug irreversibly alkylates alpha-1-adrenergic receptors on vascular smooth muscle and renders them nonfunctional, thereby causing vasodilatation. The duration of action of a single dose is approximately 24 h. Therefore, postoperative hypotension is a hazard of therapy with phenoxybenzamine if adequate plasma volume repletion is not provided. Prazosin, a short-acting, competitive alpha-1 blocker, has been used preoperatively, but has been criticized for its failure to adequately prevent perioperative hypertensive episodes. We report the case of a 73-year-old woman who was admitted for elective pheochromocytoma resection. Preoperative therapy with phenoxybenzamine was impossible because of the patient's refusal to take the drug. Preoperative antihypertensive preparation was therefore performed with prazosin 30 mg/24 h and metoprolol 100 mg/24 h. During the surgical preparation of the tumor, sodium nitroprusside was started at an average infusion rate of 4.1 micrograms/kg/min. After resection of the primary tumor, when the sodium nitroprusside infusion was stopped the patient exhibited an increase in systolic blood pressure (BP) up to 210 mg Hg. This hypertensive crisis was managed with sodium nitroprusside, nitroglycerin, and esmolol. A multilocular pheochromocytoma was diagnosed. Further stimuli due to tumour palpation resulted in repeated increases in BP. In this manner, two additional areas of tumour could be diagnosed by BP peaks after reduction of the sodium nitroprusside infusion. After complete resection of a total of three tumours, no further hypertensive crises occurred. The patient's postoperative course was uneventful. We conclude that in this patient presenting with an unsuspected multilocular pheochromocytoma, the lack of permanent alpha-blockade was probably helpful in allowing complete resection of all the tumours.

摘要

嗜铬细胞瘤是起源于嗜铬组织、能分泌儿茶酚胺的功能性肿瘤。药物治疗的主要方法是术前口服苯苄胺。该药使血管平滑肌上的α-1肾上腺素能受体不可逆地烷基化,使其失去功能,从而引起血管扩张。单次给药的作用持续时间约为24小时。因此,如果没有充分补充血容量,术后低血压是苯苄胺治疗的一个风险。哌唑嗪是一种短效竞争性α-1阻滞剂,曾用于术前治疗,但因其未能充分预防围手术期高血压发作而受到批评。我们报告一例73岁女性因择期切除嗜铬细胞瘤入院。由于患者拒绝服用苯苄胺,无法进行术前治疗。因此术前使用哌唑嗪30mg/24小时和美托洛尔100mg/24小时进行降压准备。在肿瘤手术准备过程中,开始静脉输注硝普钠,平均输注速率为4.1μg/kg/min。切除原发肿瘤后,停止输注硝普钠时,患者收缩压升至210mmHg。通过硝普钠、硝酸甘油和艾司洛尔治疗高血压危象。诊断为多房性嗜铬细胞瘤。肿瘤触诊引起的进一步刺激导致血压反复升高。通过这种方式,在硝普钠输注减少后,根据血压峰值可诊断出另外两个肿瘤区域。在总共三个肿瘤完全切除后,未再发生高血压危象。患者术后恢复顺利。我们得出结论,在该例未被怀疑有多房性嗜铬细胞瘤的患者中,缺乏永久性α受体阻滞可能有助于完整切除所有肿瘤。

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