Shoker A, Morris G, Skomro R, Laxdal V
Royal University Hospital, University of Saskatchewan, Saskatoon, Canada.
Clin Nephrol. 1996 Aug;46(2):105-11.
In adults, persistent hyperkalemic distal renal tubular acidosis in the absence of impaired renal function is an unusual abnormality usually associated with the syndromes of aldosterone deficiency or resistance. Herein, we present an adult with a clinical picture consisting of a normal blood pressure of 125/80 mmHg, normal blood volume, and glomerular filtration rate, with hyperkalemic distal renal tubular acidosis. The patent could spontaneously lower her urine pH to less than 5.5. Plasma renin activity was normal. Serum aldosterone level was appropriately elevated for the level of serum potassium. Following alkalinization of the urine, she was able to generate a urinary to blood PCO2 gradient [U-B PCO2] of 55 mmHg, and had a ten fold increased potassium secretion. After salt restriction and furosemide administration, her potassium secretion rate increased only twofold despite correction of he acidosis. The acidosis, as well as the hyperkalemia, was completely corrected after 9-alpha-Fluorohydrocortisone administration. Hydrochlorothiazide corrected the acidosis and hyperkalemia. Collectively, this picture suggests an underlying chloride shunt as the possible pathophysiological mechanism. Our case in unique in that it is not associated with hypertension.
在成年人中,无肾功能损害情况下的持续性高钾性远端肾小管酸中毒是一种不常见的异常情况,通常与醛固酮缺乏或抵抗综合征相关。在此,我们报告一名成年人,其临床表现为血压正常(125/80 mmHg)、血容量正常、肾小球滤过率正常,但患有高钾性远端肾小管酸中毒。该患者能够自发地将尿液pH值降至5.5以下。血浆肾素活性正常。血清醛固酮水平随血清钾水平适当升高。尿液碱化后,她能够产生55 mmHg的尿-血PCO₂梯度[U-B PCO₂],并且钾分泌增加了10倍。限盐并给予呋塞米后,尽管酸中毒得到纠正,但其钾分泌率仅增加了两倍。给予9-α-氟氢可的松后,酸中毒和高钾血症均完全纠正。氢氯噻嗪纠正了酸中毒和高钾血症。总体而言,这种情况提示存在潜在的氯分流作为可能的病理生理机制。我们的病例独特之处在于它与高血压无关。