Andersen Marie-Louise Elkjaer, Krag-Olsen Bente, Rittig Søren
Randers Centralsygehus, Paediatrisk Afdeling, og Arhus Universitetshospital, Skejby Sygehus.
Ugeskr Laeger. 2006 Nov 27;168(48):4220-2.
We report two cases of neonates with secondary pseudohypoaldosteronism due to pyelonephritis and congenital urinary tract malformations. Both patients presented with failure to thrive, dehydration, severe hyponatraemia and metabolic acidosis. One of the patients also developed severe hyperkalaemia. Secondary pseudohypoaldosteronism may resemble congenital adrenal hyperplasia. Early diagnosis is essential since both conditions, when untreated, are fatal, and treatment of the two differs significantly. Differential diagnosis may be achieved by acute analysis of urine culture and renal ultrasonography.
我们报告了两例因肾盂肾炎和先天性尿路畸形导致继发性假性醛固酮减少症的新生儿病例。两名患者均出现生长发育迟缓、脱水、严重低钠血症和代谢性酸中毒。其中一名患者还出现了严重的高钾血症。继发性假性醛固酮减少症可能类似于先天性肾上腺增生。早期诊断至关重要,因为这两种疾病若不治疗均会致命,且二者的治疗方法有显著差异。通过对尿培养和肾脏超声进行快速分析可实现鉴别诊断。