Kondo T, Ito F, Kihara T, Nakamura R, Goya N, Nakazawa H, Toma H
Department of Urology, Tokyo Women's Medical College
Hinyokika Kiyo. 1995 Sep;41(9):669-73.
A 69-year-old man was referred to our hospital for a left abdominal tumor measuring about 30 cm in diameter. Laboratory examination revealed an elevation of norepinephrine in plasma and of its metabolites in urine. CT scan disclosed a huge cystic tumor in the retroperitoneal space and an enlarged aortocaval lymph node, suggesting a diagnosis of malignant pheochromocytoma. The hemodynamic studies showed low blood volume and high vascular resistance, and therefore, he was treated with vasodilators and volume expansion. His hemodynamic status normalized and a complete excision was performed. Pathological examination revealed that the patient had a pheochromocytoma with metastasis to a lymph node. The total weight of the tumor was 5,930 g. Since pheochromocytomas can become a large with a risk of malignancy, they should be surgically excised as completely as possible with further treatment after making a definite diagnosis.
一名69岁男性因左侧腹部有一个直径约30厘米的肿瘤被转诊至我院。实验室检查显示血浆中去甲肾上腺素及其尿液代谢产物升高。CT扫描显示腹膜后间隙有一个巨大的囊性肿瘤以及一个增大的主动脉腔静脉淋巴结,提示诊断为恶性嗜铬细胞瘤。血流动力学研究显示血容量低和血管阻力高,因此,他接受了血管扩张剂和扩容治疗。他的血流动力学状态恢复正常,并进行了完整切除。病理检查显示患者患有嗜铬细胞瘤并伴有淋巴结转移。肿瘤总重量为5930克。由于嗜铬细胞瘤可能会增大并存在恶变风险,因此应在明确诊断后尽可能彻底地手术切除,并进行进一步治疗。