Umemoto Y, Ito T, Tsugaya M, Sakakura T, Sasaki S, Kohri K, Itoh Y, Watase H
Department of Urology, Toyokawa City Hospital.
Hinyokika Kiyo. 1998 Aug;44(8):575-7.
A 67-year-old male demonstrated a right adrenal tumor at another hospital, and consulted our hospital for surgical treatment. Abdominal computed tomography revealed a 13 x 12 cm mass in the right adrenal region. Serum and urinary adrenaline levels were high, and the catecholamine levels in the blood sample of the selective adrenal vein were also high. The tumor was 1,325 g in weight and 13 x 9 x 18 cm in diameter. Pathological diagnosis was a mixed neuroendocrine-neural tumor. It was composed of pheochromocytoma and ganglioneuroma. This combination in the adrenal gland is rare. We reviewed 3 previously reported cases of composite pheochromocytoma with gangloineuroma in the adrenal gland in the Japanese literature, and this is considered to be the fourth case.
一名67岁男性在另一家医院被诊断出患有右肾上腺肿瘤,遂来我院咨询手术治疗。腹部计算机断层扫描显示右肾上腺区域有一个13×12厘米的肿块。血清和尿液肾上腺素水平升高,选择性肾上腺静脉血样中的儿茶酚胺水平也升高。肿瘤重量为1325克,直径为13×9×18厘米。病理诊断为混合性神经内分泌-神经肿瘤。它由嗜铬细胞瘤和神经节神经瘤组成。这种肾上腺的组合很罕见。我们回顾了日本文献中先前报道的3例肾上腺嗜铬细胞瘤合并神经节神经瘤的病例,本案被认为是第四例。