Reznik V M, Griswold W R, Mendoza S A, McNeal R M
Pediatrics. 1980 Nov;66(5):784-6.
A case of Neo-Mull-Soy-induced metabolic alkalosis occurred in an 8-month-old child. This child had hypochloremic hypokalemic alkalosis as well as hyperreninemia. Initially, a diagnosis of Bartter's syndrome was made and treatment consisted of KCl replacement, indomethacin, and aspirin. In retrospect, the diagnosis of Neo-Mull-Soy induced metabolic alkalosis could have been suspected on the basis of the low chloride concentration in his urine. Proposed mechanisms for the etiology of Bartter's syndrome are reviewed. Neo-Mull-Soy induced metabolic alkalosis simulates Bartter's syndrome and supports the concept that the primary abnormality in Bartter's syndrome is chloride deficiency. The chloride deficiency in Bartter's syndrome results from a defect in active chloride transport in the thick ascending limb of the loop of Henle.
一名8个月大的儿童发生了新米尔索伊(Neo-Mull-Soy)诱导的代谢性碱中毒。该儿童患有低氯低钾性碱中毒以及高肾素血症。最初,诊断为巴特综合征,治疗包括补充氯化钾、吲哚美辛和阿司匹林。回顾来看,根据其尿液中低氯浓度,本可怀疑新米尔索伊诱导的代谢性碱中毒的诊断。文中回顾了巴特综合征病因的推测机制。新米尔索伊诱导的代谢性碱中毒模拟了巴特综合征,并支持了巴特综合征的主要异常是氯缺乏这一观点。巴特综合征中的氯缺乏是由于亨氏袢升支粗段主动氯转运缺陷所致。