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Normotensive Oversized Pheochromocytoma in Twin-Pregnancy: Analysis of Therapeutic Challenges in a Rare Case

机译:双胎妊娠的血压正常超大型嗜铬细胞瘤:罕见病例中治疗挑战的分析

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摘要

An asymptomatic, normotensive 36-year-old woman in the second trimester of a twin-gestation was diagnosed with a 11 cm adrenal pheochromocytoma. Considering the hemodynamic stability of the patient, tumor size, and gestational age, the therapeutic decision of a multidisciplinary team ensued open surgical excision without any preoperative antihypertensive preparation. Following successful removal of pheochromocytoma, the patient had a normal subsequent course of pregnancy and cesarean section delivery of healthy twins at term. This unique case of a normotensive, incidental, large-sized pheochromocytoma in a twin-pregnancy illustrates that the decisions of management in such a rare occurrence should be based on individual features of the patient. Our experience supports that α-adrenergic blockade may not be essential in normotensive pheochromocytoma in pregnancy and open-surgery remains as a safe approach in the management of large adrenal tumors in twin-pregnant patients following a multidisciplinary consultation.
机译:一名双胎妊娠中期无症状,血压正常的36岁妇女被诊断患有11厘米的肾上腺嗜铬细胞瘤。考虑到患者的血流动力学稳定性,肿瘤大小和胎龄,多学科团队的治疗决策是在没有任何术前降压准备的情况下进行开放性手术切除。成功去除嗜铬细胞瘤后,该患者足月随后的妊娠过程正常,并进行了健康双胎剖宫产。双胎妊娠中血压正常,偶发,大型嗜铬细胞瘤的这种独特情况说明,在这种罕见情况下的管理决策应基于患者的个体特征。我们的经验支持,在正常血压的嗜铬细胞瘤中,α-肾上腺素受体阻滞剂可能不是必不可少的,在多学科咨询后,开放手术仍然是处理双胎孕妇大肾上腺肿瘤的安全方法。

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