Leak D, Carroll J J, Robinson D C, Ashworth E J
Can Med Assoc J. 1977 Feb 19;116(4):371-5.
To reduce the high maternal and fetal mortality in pheochromocytoma of pregnancy, therapy is advocated with phenoxybenzamine and propranolol to obtain adequate alpha- and beta-adrenergic receptor blockade. In early pregnancy control of symptoms may be difficult, but the patient may be carried to term with such medical therapy. Delivery should be by cesarean section before the onset of labour, with, if possible, simultaneous removal of the tumour. Additional preoperative preparation with phenoxybenzamine and propranolol and careful intraoperative management are essential. During her third pregnancy a 29-year-old woman was found to have a pheochromocytoma of the left adrenal gland. After the medical therapy and preparation described, the infant was delivered by cesarean section and the mother's left adrenal gland excised. Eight-year follow-up, including during a fourth pregnancy, showed no recurrence of tumour in the mother and only mild hypertension. The infant developed normally.
为降低妊娠合并嗜铬细胞瘤时孕产妇和胎儿的高死亡率,主张使用苯苄胺和普萘洛尔进行治疗,以实现充分的α和β肾上腺素能受体阻滞。在妊娠早期,症状控制可能较为困难,但通过这种药物治疗,患者可维持至足月分娩。应在临产前进行剖宫产,如果可能的话,同时切除肿瘤。术前额外使用苯苄胺和普萘洛尔进行准备以及术中仔细管理至关重要。一名29岁女性在第三次妊娠期间被发现左肾上腺有嗜铬细胞瘤。经过上述药物治疗和准备后,通过剖宫产分娩出婴儿,并切除了母亲的左肾上腺。八年随访(包括第四次妊娠期间)显示,母亲的肿瘤未复发,仅有轻度高血压。婴儿发育正常。