Mazzocchi G, Robba C, Gottardo G, Meneghelli V, Nussdorfer G G
J Submicrosc Cytol. 1982 Jan;14(1):179-85.
Two adrenocortical adenomata causing Conn's syndrome were examined by electron microscopy. Adenomatous cells were arranged in small clusters and showed a rather different morphology, especially as far as mitochondria were concerned. Some cells contained mitochondria with lamellar and tubular cristae (zone glomerulosa-like cells), while other parenchymal elements displayed mitochondria with tubular and vesicular cristae (zona fasciculata-like cells). Both cells types were endowed with a quite well developed smooth endoplasmic reticulum, some lipid droplets and a prominent Golgi apparatus. Moreover, adenomatous cells with large masses of lipofuscin pigment granules were also observed (zona reticularis-like cells). These findings stress the structural heterogeneity of the Conn's adenomata.
对两例导致原发性醛固酮增多症的肾上腺皮质腺瘤进行了电子显微镜检查。腺瘤细胞呈小簇状排列,表现出相当不同的形态,尤其是在线粒体方面。一些细胞含有具有板层状和管状嵴的线粒体(球状带样细胞),而其他实质成分则显示具有管状和泡状嵴的线粒体(束状带样细胞)。两种细胞类型均具有发育良好的滑面内质网、一些脂滴和一个突出的高尔基体。此外,还观察到含有大量脂褐素色素颗粒的腺瘤细胞(网状带样细胞)。这些发现强调了原发性醛固酮增多症腺瘤的结构异质性。