首页> 外文期刊>Canadian journal of surgery: Journal canadien de chirurgie >Laparoscopic adrenalectomy for pheochromocytoma in pregnancy.
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Laparoscopic adrenalectomy for pheochromocytoma in pregnancy.

机译:腹腔镜肾上腺切除术治疗妊娠嗜铬细胞瘤。

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A 28-year-old woman was diagnosed with right adrenal pheochromocytoma on the basis of episodes of nausea, bloating and headaches, and elevated 24-hour urine metanephrines, normetanephrines and epinephrine. Imaging studies included ultrasonography, computed tomography and a rnetaiodobenzylguani-dine (MIBG) scan. Serum calcium, calcitonin, renin and aldosterone levels were normal, as were the results of a low-dose dexamethasone test and a thyroid-stimulating hormone test. Genetic testing for multiple endocrine neoplasia, type 2 and von Hippel-Lindau disease was negative. Two weeks after the diagnosis, the patient discovered that she was pregnant. She was subsequently taken off prazosin and referred to both an obstetrician who specialized in high-risk pregnancy and a laparoscopic surgeon. The patient underwent an uncomplicated laparoscopic right adrenalectomy at 16 weeks' gestation. This led to resolution of symptoms and biochemical abnormalities and delivery of a healthy son at term. Pathological analysis confirmed the diagnosis of pheochromocytoma with minimal cy-tological pleomorphism and no extension outside the adrenal gland; these findings are consistent with the presence of a benign lesion.
机译:一名28岁的女性因恶心,腹胀和头痛以及24小时尿中肾上腺素,去甲肾上腺素和肾上腺素升高而被诊断出患有右肾上腺嗜铬细胞瘤。影像学研究包括超声检查,计算机断层扫描和雷诺碘苄基胍(MIBG)扫描。血清钙,降钙素,肾素和醛固酮水平正常,低剂量地塞米松试验和促甲状腺激素试验的结果也正常。多发性内分泌肿瘤,2型和von Hippel-Lindau病的基因检测为阴性。诊断后两周,患者发现她已怀孕。随后,她被撤下了哌唑嗪,并转诊给专门从事高危妊娠的妇产科医生和腹腔镜外科医生。该患者在妊娠16周时进行了简单的腹腔镜右肾上腺切除术。这导致症状和生化异常的缓解以及足月生一个健康的儿子。病理分析证实了嗜铬细胞瘤的诊断具有最小的细胞学多态性,并且没有在肾上腺外扩展;这些发现与良性病变的存在是一致的。

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