Department of Neurology, The Second Xiangya Hospital, Central South University, Changsha, China.
Acta Neurol Scand. 2018 Jul;138(1):4-11. doi: 10.1111/ane.12938. Epub 2018 Apr 14.
Hyponatremia is a potentially serious electrolyte abnormality observed in neuromyelitis optica spectrum disorders (NMOSDs), and its most common cause is syndrome of inappropriate antidiuretic hormone secretion (SIADH). Another potential cause of hyponatremia is cerebral salt-wasting syndrome (CSWS), although CSWS has not previously been reported in NMOSDs. Accurate and early differentiation between SIADH and CSWS is difficult. However, the two conditions have important implications for the selection of therapy. Here, we describe two patients with aquaporin-4 antibody (AQP4-Ab)-positive NMOSDs who developed hyponatremia as a result of CSWS and SIADH, respectively. Additionally, we review all previously reported studies of hyponatremia in patients with NMOSDs and propose several potential pathophysiological mechanisms of hyponatremia. In conclusion, NMOSDs accompanied by hyponatremia are not actually rare, but have previously been given little attention. Furthermore, SIADH should not be the only consideration, before the exclusion of rare but significant CSWS.
低钠血症是视神经脊髓炎谱系疾病(NMOSD)中一种潜在的严重电解质异常,其最常见的原因是抗利尿激素分泌不当综合征(SIADH)。低钠血症的另一个潜在原因是脑性盐耗综合征(CSWS),尽管 CSWS 以前从未在 NMOSD 中报道过。准确和早期区分 SIADH 和 CSWS 很困难。然而,这两种情况对治疗方案的选择有重要意义。在这里,我们描述了两名水通道蛋白 4 抗体(AQP4-Ab)阳性 NMOSD 患者,他们分别因 CSWS 和 SIADH 而出现低钠血症。此外,我们回顾了所有以前报道的 NMOSD 患者低钠血症的研究,并提出了低钠血症的几个潜在病理生理机制。总之,伴有低钠血症的 NMOSD 实际上并不罕见,但以前很少受到关注。此外,在排除罕见但严重的 CSWS 之前,不应该只考虑 SIADH。