Block M A, Jackson C E, Tashjian A H
Arch Surg. 1975 May;110(5):617-24. doi: 10.1001/archsurg.1975.01360110163027.
Of 13 patients treated surgically for familial medullary thyroid carcinoma in whom parathyroid tissue was availabe, the majority showed parathyroid abnormalities (hyperplasia in sis, tumors in five). Two patients had had renal calculi. No correlation was evident between the presence of the parathyroid tumors and peripheral blood levels of parathyroid hormone. Hyperparathyroidism is usually mild, but occasionally it results in complications of hypercalcemia. Hyperparathyroidism has not appeared to date following removal of medullary thyroid carcinoma associated with normal-sized but microscopically hyperplastic parathyroids. Evidence of parathyroid abnormalities has not been recognized in eight patients with sporadic medullary carcinoma, making genetic factors dominant in explaining the association of parathyroid hyperplasia and this carcinoma. At operation, parathyroid glands should be evaluated and those that are grossly enlarged removed while preserving parathyroid function.
在13例接受手术治疗的家族性甲状腺髓样癌患者中,有甲状旁腺组织可供研究,大多数患者显示甲状旁腺异常(6例增生,5例肿瘤)。2例患者有肾结石。甲状旁腺肿瘤的存在与甲状旁腺激素外周血水平之间无明显相关性。甲状旁腺功能亢进通常较轻,但偶尔会导致高钙血症并发症。在切除甲状腺髓样癌后,与正常大小但显微镜下增生的甲状旁腺相关的甲状旁腺功能亢进迄今尚未出现。8例散发性甲状腺髓样癌患者未发现甲状旁腺异常证据,这表明遗传因素在解释甲状旁腺增生与这种癌症的关联中占主导地位。手术时,应评估甲状旁腺,切除明显肿大的甲状旁腺,同时保留甲状旁腺功能。