Sharra Irida, Lhoir Marine, Des Grottes Jean-Marin, Vaes Melanie, Guerisse Fabien
Emergency Department, CHU Charleroi-Chimay, Charleroi, BEL.
Nephrology Department, CHU Tivoli, La Louvière, BEL.
Cureus. 2024 Aug 4;16(8):e66118. doi: 10.7759/cureus.66118. eCollection 2024 Aug.
Fanconi syndrome (FS) is a complex disorder characterized by a reabsorption defect in the proximal renal tubule (PT), leading to urinary loss of molecules such as glucose, phosphate, calcium, amino acids, bicarbonate, potassium, and low-molecular-weight proteins. Its etiology can be genetic or acquired, with drug toxicity being a significant cause of the acquired forms. The heterogeneous manifestations of FS, whether in its partial or complete form, can pose challenges in the emergency department; nevertheless, it should be considered in certain patients, as understanding its cause is crucial for initiating effective treatment. We present the case of a 59-year-old female patient with FS who was treated with lenalidomide in the context of stage III IgG kappa multiple myeloma according to the Salmon Durie classification. We highlight the recurrent nature of this syndrome in this patient.
范科尼综合征(FS)是一种复杂的病症,其特征为近端肾小管(PT)重吸收缺陷,导致葡萄糖、磷酸盐、钙、氨基酸、碳酸氢盐、钾和低分子量蛋白质等分子从尿液中流失。其病因可以是遗传性的或后天获得性的,药物毒性是后天性形式的一个重要原因。FS的异质性表现,无论是部分形式还是完全形式,在急诊科都可能带来挑战;然而,在某些患者中应考虑到这一点,因为了解其病因对于启动有效治疗至关重要。我们报告一例59岁女性FS患者的病例,该患者根据萨尔蒙·杜里分类法,在III期IgG κ型多发性骨髓瘤的情况下接受了来那度胺治疗。我们强调了该综合征在该患者中的复发性。