Hasleton P S, Ali H H
J Pathol. 1980 Dec;132(4):307-23. doi: 10.1002/path.1711320403.
The parathyroids from ten consecutive cases of chronic renal failure coming to operation in a period of seven years were studied by light and electron microscopy. The clinical and biochemical data as well as the levels of immunoreactive parathormone (iPTH) were reviewed. For the sake of comparison adenomata from two cases of primary hyperparathyroidism were studied. In the cases of chronic ;renal failure there were six cases of tertiary hyperparathyroidism with adenoma formation, surrounded by dense fibrous tissue and compression of adjacent parathyroid cell amidst a background of hyperplasia. Two cases showed secondary parathyroid hyperplasia and the remaining two cases were adenomata which clinically affected only one gland. Neither the biochemical data nor levels of iPTH allowed the cases with secondary hyperplasia to be separated from those with tertiary hyperparathyroidism. Similarly electron microscopy showed no distinct differences between these two groups of adenomata from cases of primary hyperparathyroidism. The diagnosis of tertiary hyperparathyroidism is made on a combination of clinical, biochemical and histological features, the histological features being most important. It is concluded that tertiary hyperparathyroidism is part of a histological spectrum in response to chronic renal failure and autonomous glands are related to the mass of parathyroid tissue present.
对7年间连续接受手术的10例慢性肾衰竭患者的甲状旁腺进行了光镜和电镜研究。回顾了临床和生化数据以及免疫反应性甲状旁腺激素(iPTH)水平。为作比较,研究了2例原发性甲状旁腺功能亢进患者的腺瘤。在慢性肾衰竭病例中,有6例为伴有腺瘤形成的三发性甲状旁腺功能亢进,腺瘤被致密纤维组织包绕,周围甲状旁腺细胞受压,背景为增生。2例表现为继发性甲状旁腺增生,其余2例为腺瘤,临床上仅累及一个腺体。生化数据和iPTH水平均无法将继发性增生病例与三发性甲状旁腺功能亢进病例区分开来。同样,电镜检查显示,原发性甲状旁腺功能亢进病例的这两组腺瘤之间无明显差异。三发性甲状旁腺功能亢进的诊断基于临床、生化和组织学特征的综合判断,其中组织学特征最为重要。得出的结论是,三发性甲状旁腺功能亢进是对慢性肾衰竭反应的组织学谱的一部分,自主性腺体与甲状旁腺组织的量有关。