Greathouse D J, McDermott M T, Kidd G S, Hofeldt F D
Am J Med. 1984 Jun;76(6):1132-6. doi: 10.1016/0002-9343(84)90870-2.
A 47-year-old woman is described who had pure primary hyperaldosteronism due to an adrenal cortical carcinoma. This may represent the first such case in which modern laboratory tests allowed specific diagnosis and exclusion of hypersecretion of other adrenal steroids, and also the first reported case in which modern localizing procedures have been utilized. Other interesting facets of the case include calcification of the tumor, visualization with 131l iodomethylnorcholesterol , metaplastic histologic changes, and coexistent bilateral renal artery fibromuscular disease.
本文描述了一名47岁女性,她因肾上腺皮质癌患有单纯性原发性醛固酮增多症。这可能是首例通过现代实验室检查得以进行特异性诊断并排除其他肾上腺类固醇激素分泌过多的此类病例,也是首例报道运用现代定位检查方法的病例。该病例其他有趣的方面包括肿瘤钙化、用131I-碘甲基胆固醇显像、化生的组织学改变以及并存的双侧肾动脉纤维肌性疾病。