Ohzeki T, Hanaki K, Asano T, Ishitani N, Wakatsuki H, Shiraki K
Acta Paediatr Scand. 1986 Nov;75(6):1046-50. doi: 10.1111/j.1651-2227.1986.tb10341.x.
A case of hypodipsic hypernatremia in a 16-month-old Japanese boy is reported. Partial antidiuretic hormone deficiency was present. Computed tomography of the brain revealed absence of septum lucidum. No ophthalmological abnormality could be found. He had hyposmia, which has not been reported previously in association with hypernatremia due to hypodipsia. Forced fluid administration and nasal 1-deamino-8-d-arginine vasopressin treatment could maintain serum electrolyte levels within normal ranges. However, episodes of hypernatremia could not be completely avoided while he was treated with 1-deamino-8-d-arginine vasopressin and ad libitum oral fluid.
报告了一名16个月大日本男孩的低渗性高钠血症病例。存在部分抗利尿激素缺乏。脑部计算机断层扫描显示透明隔缺失。未发现眼科异常。他嗅觉减退,此前尚未有因饮水过少导致高钠血症而伴有嗅觉减退的报道。强制补液和鼻腔给予1-去氨基-8-D-精氨酸加压素治疗可使血清电解质水平维持在正常范围内。然而,在用1-去氨基-8-D-精氨酸加压素和随意口服液体治疗期间,高钠血症发作仍无法完全避免。