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
{"title":"Hungry Bone Syndrome after Surgical Treatment of Hyperparathyroidism in Dialysis Patients: About Two (2) Cases in Senegal","authors":"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","doi":"10.22259/2639-3573.0301004","DOIUrl":null,"url":null,"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.","PeriodicalId":93415,"journal":{"name":"Archives of nephrology & urology studies","volume":"25 1","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2020-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Archives of nephrology & urology studies","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.22259/2639-3573.0301004","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0
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.