Akhanlı Pınar, Hepsen Sema, Ucan Bekir, Saylam Güleser, Cakal Erman
AACE Clin Case Rep. 2020 Aug 6;6(6):e319-e321. doi: 10.4158/ACCR-2020-0113. eCollection 2020 Nov-Dec.
Hypercalcemia associated with the use of sodium-glucose transporter-2 (SGLT-2) inhibitors is very rare. Only 2 cases have been reported in the current literature. In these cases hypercalcemia occurred with the use of SGLT-2 inhibitors taken with thiazides and excessive calcium salts. We present a case of hypercalcemia and primary hyperparathyroidism diagnosed after dapagliflozin treatment.
We describe the medical history, laboratory test results, parathyroid ultrasound, 4-dimensional computed tomography-magnetic resonance imaging, and histopathology findings of the patient.
A 49-year-old man with 5-year history of type 2 diabetes mellitus was found to have hypercalcemia with corrected calcium of 11.28 mg/dL (reference range [RR] is 8.8 to 10.6 mg/dL) 6 months after starting dapagliflozin. Previous records showed normocalcemia for many years. Parathyroid hormone level was 70.8 pg/mL (RR is 15 to 65 pg/mL) and 24-hour urinary calcium excretion level was 492 mg/day (RR is 100 to 300 mg/day). On parathyroid ultrasound, a 4 × 9 × 14-mm hypoechoic lesion inferior to the right thyroid lobe was detected. A 15 × 10 × 9-mm oval lesion was observed in the right paratracheal area. A lesion at T1 vertebra level was also seen on 4-dimensional computed tomography-magnetic resonance imaging. The patient underwent lower right parathyroidectomy. Histopathology confirmed the diagnosis of parathyroid adenoma. The patient was asymptomatic 3 months after the operation with a normal corrected calcium level of 9.2 mg/dL.
SGLT-2 inhibitors could have unmasked an underlying mild hyperparathyroidism, as they can increase predisposition to hypercalcemia when used with medications causing it. Volume depletion caused by SGLT-2 inhibitors may also contribute to hypercalcemia. For these reasons, calcium levels should be monitored in patients taking SGLT-2 inhibitors.
与使用钠-葡萄糖协同转运蛋白2(SGLT-2)抑制剂相关的高钙血症非常罕见。目前文献中仅报道了2例。在这些病例中,高钙血症发生于SGLT-2抑制剂与噻嗪类药物及过量钙盐联用时。我们报告1例在达格列净治疗后诊断为高钙血症和原发性甲状旁腺功能亢进的病例。
我们描述了该患者的病史、实验室检查结果、甲状旁腺超声、四维计算机断层扫描-磁共振成像以及组织病理学检查结果。
一名患有2型糖尿病5年的49岁男性,在开始使用达格列净6个月后被发现血钙升高,校正血钙为11.28mg/dL(参考范围[RR]为8.8至10.6mg/dL)。既往记录显示多年来血钙正常。甲状旁腺激素水平为70.8pg/mL(RR为15至65pg/mL),24小时尿钙排泄水平为492mg/天(RR为100至300mg/天)。甲状旁腺超声检查发现右甲状腺叶下方有一个4×9×14mm的低回声病变。在右气管旁区域观察到一个15×10×9mm的椭圆形病变。四维计算机断层扫描-磁共振成像在T1椎体水平也发现了一个病变。患者接受了右下甲状旁腺切除术。组织病理学确诊为甲状旁腺腺瘤。术后3个月患者无症状,校正血钙水平正常,为9.2mg/dL。
SGLT-2抑制剂可能会掩盖潜在的轻度甲状旁腺功能亢进,因为它们与导致高钙血症的药物联用时会增加发生高钙血症的易感性。SGLT-2抑制剂引起的容量耗竭也可能导致高钙血症。出于这些原因,服用SGLT-2抑制剂的患者应监测血钙水平。