Hyperparathyroidism with normal albumin-corrected total calcium in patients with multiple endocrine neoplasia type 1.

Henry Ford Hospital medical journal Pub Date : 1992-01-01
J J Shepherd, B T Teh, V Parameswaran, R David
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Abstract

In the largest reported family of patients with multiple endocrine neoplasia type 1 (MEN 1), hyperparathyroidism was expressed at first screening in 33 patients by elevation of ionized calcium (IC) (30 cases) or parathyroid hormone (three cases) without elevation of albumin-corrected total calcium (ACTC). Three of these 33 patients have shown a progressive rise in IC and later an elevation of ACTC. However, the age distribution suggests that in others the level of IC may remain stable at a minimally elevated level throughout life with ACTC remaining normal except for transient rises at the times of intercurrent illness or surgical operation. Even when ACTC is normal preoperatively, patients with an elevation of IC require radical subtotal parathyroidectomy or total parathyroidectomy and forearm implantation to restore IC to a normal level. Institutions that rely on ACTC as a screening test for hyperparathyroidism in MEN 1 will miss the diagnosis in nearly half of patients under the age of 30. The greatest deficiency in using ACTC occurs in the follow-up of patients who have undergone parathyroidectomy for MEN 1. Only three of 11 recurrences were evidenced by this measurement.

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多发性内分泌肿瘤1型患者甲状旁腺功能亢进伴白蛋白校正总钙正常。
在最大的多发性内分泌肿瘤1型(MEN 1)患者家族中,33例患者在首次筛查时通过离子钙(IC)(30例)或甲状旁腺激素(3例)升高表达甲状旁腺功能亢进,而没有白蛋白校正总钙(ACTC)升高。这33例患者中有3例表现为IC的进行性升高,随后ACTC升高。然而,年龄分布表明,在其他患者中,IC水平可能在一生中保持稳定在最低水平,ACTC保持正常,除了在疾病或外科手术时短暂上升。即使术前ACTC正常,IC升高的患者也需要根治性甲状旁腺次全切除术或甲状旁腺全切除术和前臂植入术来恢复IC到正常水平。依靠ACTC作为男性甲状旁腺功能亢进症筛查试验的机构在30岁以下的患者中有近一半会漏诊。ACTC使用的最大缺陷发生在对接受甲状旁腺切除术的男性患者的随访中。11次重复中只有3次被这种测量证明。
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Extracellular Ca2+ sensing in C-cells and parathyroid cells. Proceedings of the Urban Health Care Symposium II. June 2-4, 1991. Characterization of the clinical features of five families with hereditary primary cutaneous lichen amyloidosis and multiple endocrine neoplasia type 2. Unusual features of multiple endocrine neoplasia. Long-term follow-up in four large MEN 2 families in The Netherlands.
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