Marinescu I, Stefănescu A M
Endocrinologie. 1985 Jan-Mar;23(1):61-6.
Pheochromocytoma was diagnosed in a female patient aged 26 with paroxysmal arterial hypertension (AH), profuse sweating, headache, anxiety, tachycardia, transit arrhythmia, high urinary norepinephrine (NE), epinephrine (E) and vanillyl mandelic acid (VMA). Urography with intravenous Odiston revealed a relatively large tumor at the upper pole of the right kidney. Complete removal of the tumor in a 2-step surgical procedure brings apparent clinical and hormonal recovery for 6 years, but then clinical and hormonal relapse occurs through ganglionary metastasis and tumor at the basis of the mesentery. Removal of the metastasis and tumor brings again improvement in the clinical and hormonal picture.
一名26岁女性患者被诊断为嗜铬细胞瘤，伴有阵发性动脉高血压（AH）、多汗、头痛、焦虑、心动过速、短暂性心律失常、尿去甲肾上腺素（NE）、肾上腺素（E）和香草扁桃酸（VMA）水平升高。静脉注射欧乃派克进行的尿路造影显示右肾上极有一个相对较大的肿瘤。通过两步手术程序完全切除肿瘤后，患者在6年内临床症状和激素水平明显恢复，但随后通过神经节转移和肠系膜根部肿瘤出现临床和激素复发。切除转移灶和肿瘤后，临床症状和激素情况再次改善。
