CKD G5D患者高钙血症的鉴别诊断

A. Eremkina, A. Gorbacheva, Daria V. Lisina, A. Povaliaeva, A. Ekaterina, Pigarova, N. Mokrysheva
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引用次数: 1

摘要

慢性肾脏病患者的特征是由于功能性肾单位数量的减少而发展为矿物质障碍。这些变化表现为继发性甲状旁腺功能亢进(与血清低钙血症、高磷血症相关的完整甲状旁腺激素(PTH)的过度产生)、维生素D代谢紊乱、骨矿化以及骨外钙化。与高钙血症相关的血清PTH水平降低对于无动力性骨病是可疑的,但同时需要扩展鉴别诊断搜索(例如转移过程)。高钙血症的一个罕见原因是24-羟化酶(CYP24A1)缺陷。我们报告了一例血液透析患者,患有非典型继发性甲状旁腺功能亢进症和CYP24A1缺陷。
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Differential diagnosis of hypercalcemia in a patient with CKD G5D
Patients with chronic kidney disease are characterized by the development of mineral disorders due to a decrease in the number of functioning nephrons. These changes manifest by the development of secondary hyperparathyroidism (the overproduction of intact parathyroid hormone (PTH) associated with the serum hypocalcemia, hyperphosphatemia), dysfunctional vitamin D metabolism, bone mineralization and also extraosseous calcifications. Decreased serum PTH levels associated with hypercalcemia are suspicious for adynamic bone disease, but at the same time requires an extended differential diagnostic search (e.g. metastatic processes). One of the rare causes of hypercalcemia is a defect in 24-hydroxylase (CYP24A1). We present a case of a patient on hemodialysis with atypical secondary hyperparathyroidism and an established CYP24A1 defect.
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Obesity and Metabolism-Milan
Obesity and Metabolism-Milan 医学-内分泌学与代谢
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