Hungry Bone Syndrome after Surgical Treatment of Hyperparathyroidism in Dialysis Patients: About Two (2) Cases in Senegal

N. Keita, S. Diagne, M. Faye, M. Faye, B. Ba, A. Tall Lemrabott, M. Mbengue, A. Dieng, Mamadou Aw Ba, A. Sy, B. Ndiaye, M. Ndongo, El Hadji Fary Ka
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Abstract

Introduction: Hungry bone syndrome (HBS) is a complication of hyperparathyroidism surgical management characterized by deep hypocalcaemia and hypophosphatemia secondary to a massive influx of calcium to an avid bone. Observations: We report the cases of two (2) patients dialysed for chronic kidney disease (CKD) whose initial nephropathy is a hypertensive nephropathy. They posed the problem of CKD-mineral bone disorder (CKD-MBD) fibrous osteitis type with intact parathyroid hormone (PTH) up to 40N for which a subtotal parathyroidectomy (PTX) was performed with postoperative biological anomalies in favour of the diagnosis of hungry bone syndrome. Conclusion: HBS still intervenes on osteopathies of intense turnover. Its treatment is difficult, based on prolonged calcium and vitamin D supplementation. However, perioperative therapeutic protocols settlement seems essential in order to minimize the risks of its occurrence.
透析患者甲状旁腺功能亢进手术治疗后的饥饿骨综合征:塞内加尔约2例
饥饿骨综合征(HBS)是甲状旁腺功能亢进手术治疗的一种并发症,以深度低钙血症和低磷血症为特征,继发于大量钙流入饥饿骨。观察:我们报告了两(2)例慢性肾脏疾病(CKD)透析患者,其初始肾病是高血压肾病。他们提出了ckd -矿物骨障碍(CKD-MBD)纤维性骨炎类型的问题,甲状旁腺激素(PTH)完整,高达40N,甲状旁腺次全切除术(PTX)进行了术后生物学异常,有利于饥饿骨综合征的诊断。结论:HBS仍可干预强烈翻转的骨病。它的治疗很困难,需要长期补充钙和维生素D。然而,围手术期的治疗方案似乎是必要的,以尽量减少其发生的风险。
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