Kalashnikov S A, Lisochkin B G
Arkh Patol. 1986;48(10):47-53.
Having studied the results of investigation of 132 patients with Icenko-Cushing syndrome (68 out of them with different structural variants of adrenal tumours, 68--without adrenal tumours), the authors came to the conclusion that adenomas of dark and mixed polymorphic cells belong to hormonally active adrenal tumours, while light-cell monomorphic adenomas belong to hormonally inactive tumours. An electron-microscopic study provides identification of signs of functional activity in adenomas and cancer tumours, to clear up the additional criteria of anaplasia in them. In patients with Icenko-Cushing syndrome, but without a tumour in the adrenal cortex ultrastructural changes in corticocytes are characteristic of the increase of cellular proliferation and the decrease of incretory activity. The follow-up results of surgical treatment were studied in all cases.
在对132例艾兴科-库欣综合征患者(其中68例患有不同结构变异的肾上腺肿瘤,68例无肾上腺肿瘤)的调查结果进行研究后,作者得出结论,深色和混合多形性细胞腺瘤属于有激素活性的肾上腺肿瘤,而亮细胞单形性腺瘤属于无激素活性的肿瘤。电子显微镜研究有助于识别腺瘤和癌瘤中的功能活性迹象,以明确其中间变的附加标准。在艾兴科-库欣综合征患者中,但肾上腺皮质无肿瘤,皮质细胞的超微结构变化特征为细胞增殖增加和分泌活性降低。对所有病例的手术治疗随访结果进行了研究。