Holmlund D, Boquist L, Larsson S E, Lorentzon R
Acta Chir Scand. 1979;145(1):27-33.
Parathyroid morphology and blood chemistry were studied in five patients with primary hyperparathyroidism treated with 1,25-dihydroxycholecalciferol (1,25-DHCC) for 2 to 11 days before planned operation. Before the institution of treatment all patients were hypercalcemic, whereas the serum immunoreactive parathyroid hormone (iPTH) concentration either was elevated or normal. During the treatment the urinary phosphate excretion was significantly increased, whereas the calcium excretion and the serum concentrations of calcium and phosphate were unaffected or only slightly changed. Serum iPTH decreased during the first days of treatment, but returned then to increased levels close to the pretreatment ones. The treatment was tolerated well by the patients. Light and electron microscopy of the removed parathyroid glands disclosed one adenoma in each of the five patients, the other glands exhibiting either a slight hyperplasia or a normal appearance. Both the adenomatous and the non-adenomatous parathyroid tissue showed a predominance of dark chief cells and three of the adenomas exhibited a varying number of atrophic and oxyphil cells. The non-adenomatous glands were composed of atrophic and dark chief cells. Signs of low functional activity were ultrastructurally observed in the parathyroid parenchymal cells. It is suggested that 1,25-DHCC treatment of patients with primary hyperparathyroidism inhibits parathyroid hormone secretion.
在五例原发性甲状旁腺功能亢进患者中,于计划手术前给予1,25 - 二羟胆钙化醇(1,25 - DHCC)治疗2至11天,对甲状旁腺形态和血液化学指标进行了研究。在开始治疗前,所有患者均有高钙血症,而血清免疫反应性甲状旁腺激素(iPTH)浓度要么升高,要么正常。治疗期间,尿磷排泄显著增加,而钙排泄以及血清钙和磷浓度未受影响或仅有轻微变化。血清iPTH在治疗的头几天下降,但随后又回升至接近治疗前的升高水平。患者对该治疗耐受性良好。对切除的甲状旁腺进行光镜和电镜检查发现,五例患者中每例均有一个腺瘤,其他腺体表现为轻度增生或外观正常。腺瘤性和非腺瘤性甲状旁腺组织均以暗主细胞为主,其中三个腺瘤有不同数量的萎缩细胞和嗜酸性细胞。非腺瘤性腺体由萎缩的暗主细胞组成。在甲状旁腺实质细胞中观察到超微结构的低功能活性迹象。提示1,25 - DHCC治疗原发性甲状旁腺功能亢进患者可抑制甲状旁腺激素分泌。