Wajiki M, Ogawa A, Fukui J, Komiya I, Yamada T, Maruyama Y
J Surg Oncol. 1985 Jan;28(1):75-8. doi: 10.1002/jso.2930280118.
An extremely rare case is reported in which aldosteronoma and pheochromocytoma coexisted in an adrenal gland. Although the patients presented with clinical features of primary aldosteronism, preoperative examination showed an elevation of both plasma aldosterone and urinary catecholamines. Histology of the removed adrenal gland revealed that, concurrently with a round mass of adrenocortical adenoma, the adrenal medulla was totally occupied by the typical structure of pheochromocytoma.
报道了一例极为罕见的病例，肾上腺中醛固酮瘤和嗜铬细胞瘤共存。尽管患者表现出原发性醛固酮增多症的临床特征，但术前检查显示血浆醛固酮和尿儿茶酚胺均升高。切除肾上腺的组织学检查显示，在肾上腺皮质腺瘤的圆形肿块旁，肾上腺髓质完全被嗜铬细胞瘤的典型结构占据。
