Szabó D, Gyévai A, Gláz E, Stark E, Péteri M, Alánt O
Morphol Igazsagugyi Orv Sz. 1975 Oct;15(4):243-8.
Tissue cultures of a surgically removed adrenocortical tumour causing Cushing's syndrome, and tissue cultures from the attached, tumour-free adrenal were studied. There were two cell types characteristic of tumour tissue. The cell type occurring most frequently had pronounced hypertrophied agranular endoplasmic reticulum. A fewer number of lipidrich cells containing many electron-dense granules could also be found. The ratio of cells changed during cultivation. In the 17 days tumour culture, a higher percentage of lipid-rich cells could be observed. In spite of continuous ACTH treatment, the initially high hydrocortisone level decreased, gradually. It may be assumed that the lipid-rich cells are of reduced ability as regards hydrocortisone production.
对一例因库欣综合征而手术切除的肾上腺皮质肿瘤的组织培养物,以及来自相连的无肿瘤肾上腺的组织培养物进行了研究。肿瘤组织有两种特征性细胞类型。最常见的细胞类型具有明显肥大的无颗粒内质网。也能发现少量含有许多电子致密颗粒的富含脂质的细胞。细胞比例在培养过程中发生变化。在17天的肿瘤培养中,可以观察到更高比例的富含脂质的细胞。尽管持续给予促肾上腺皮质激素(ACTH)治疗,最初较高的氢化可的松水平仍逐渐下降。可以推测,富含脂质的细胞在氢化可的松产生方面的能力降低。