首页> 外文期刊>Canadian Journal of Kidney Health and Disease >PTHrP-related Hypercalcaemia in Infancy and Congenital Anomalies of the Kidney and Urinary Tract (CAKUT)
【24h】

PTHrP-related Hypercalcaemia in Infancy and Congenital Anomalies of the Kidney and Urinary Tract (CAKUT)

机译:婴儿和先天性肾脏和尿路异常中的PTHrP相关高钙血症(CAKUT)

获取原文
       

摘要

BackgroundSevere hypercalcaemia is a rare but clinically significant condition in infancy and childhood. Parathyroid hormone-related peptide (PTHrP)-mediated hypercalcaemia resulting from a malignancy is rare and only a handful of case reports have outlined its incidence alongside a benign condition. ObjectivesTo describe the diagnostic workup and management of an infant with hypercalcaemia, renal dysplasia, and elevated PTHrP levels. DesignCase report. SettingThe Victoria Hospital campus of the London Health Sciences Centre in London, Ontario, Canada. PatientsA child with congenital anomalies of the kidneys and urinary tract (CAKUT), stage 2 chronic kidney disease (CKD), and renal dysplasia who presented with severe hypercalcaemia. MeasurementsWeight, renal ultrasound, creatinine, cystatin C, eGFR, calcium, urea, bicarbonate, serum sodium, fractional sodium excretion, urine calcium to creatinine ratio, PTH, TSH, Free T4, AM cortisol, HMA, VMA, 25-vitamin D, 1,25 dihydroxy-vitamin D, calcitriol, vitamin A, ACE levels, skull and chest x-rays, alkaline phosphatase, CBC, tumour lysis profile, catecholamine breakdown, whole-body MRI, PTHrP. MethodsFull diagnostic workup and patient management. Patient treated with intravenous hydration, furosemide, calcitonin and CalciLo. ResultsPTHrP was elevated and no evidence of a malignancy was found. Treatment consisting of a low-calcium CalciLo diet (in place of breast milk) adequately controlled the patient’s hypercalcaemia. Hypercalcaemia associated with CAKUT in infancy is not all that uncommon and was reported in 15/99 infants in another study, most of whom had a suppressed PTH similar to that of our patient. PTHrP was not measured in these cases and may have also been elevated. LimitationsThe study is limited in that it is a description of a single patient case. Future measurement of PTHrP in similar patients is necessary to confirm our results. ConclusionsThe possibility of elevated PTHrP levels must be considered in patients with known renal dysplasia who are differentially diagnosed with hypercalcaemia.
机译:背景严重的高钙血症在婴儿期和儿童期是一种罕见但具有临床意义的疾病。由恶性肿瘤引起的甲状旁腺激素相关肽(PTHrP)介导的高钙血症很少见,只有少数病例报告概述了其发病率以及良性疾病。目的描述高钙血症,肾发育不良和PTHrP水平升高的婴儿的诊断检查和处理。 DesignCase报告。设置加拿大安大略省伦敦市伦敦健康科学中心的维多利亚医院校园。患者患有先天性肾脏和泌尿道异常(CAKUT),2期慢性肾脏病(CKD)和肾发育不良的儿童,伴有严重的高钙血症。体重,肾脏超声,肌酐,半胱氨酸蛋白酶抑制剂C,eGFR,钙,尿素,碳酸氢盐,血清钠,钠分数排泄,尿钙与肌酐之比,PTH,TSH,游离T4,AM皮质醇,HMA,VMA,25种维生素D, 1,25二羟基维生素D,骨化三醇,维生素A,ACE水平,头骨和胸部X射线,碱性磷酸酶,CBC,肿瘤溶解情况,儿茶酚胺分解,全身MRI,PTHrP。方法全面的诊断检查和患者管理。接受静脉水合作用,速尿,降钙素和降钙素治疗的患者。结果PTHrP升高,未发现恶性肿瘤的证据。低钙CalciLo饮食(代替母乳)组成的治疗可以充分控制患者的高钙血症。婴儿期CAKUT引起的高钙血症并非很常见,另一项研究报道了15/99婴儿,其中大多数人的PTH抑制与本患者相似。在这些情况下未测量PTHrP,也可能升高了。局限性该研究的局限性在于它仅描述单个患者的病例。有必要对类似患者中的PTHrP进行进一步测量,以证实我们的结果。结论在已知有肾钙异常增生的患者中,PTHrP水平升高的可能性必须予以鉴别诊断为高钙血症。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号