对乙酰氨基酚
医学
代谢性酸中毒
内科学
尿
谷胱甘肽
肝功能
毒性
排泄
酸中毒
胆红素
肝功能检查
内分泌学
胃肠病学
药理学
酶
生物化学
生物
作者
Ayşegül Tokatlı,Kalkanoğlu-Sivri Hs,Abdurrauf Yüce,Teoman Coşkun
出处
期刊:PubMed
日期:2007-05-24
卷期号:49 (1): 75-6
被引量:11
摘要
We report a patient with glutathione synthetase (GS) deficiency who developed acetaminophen-induced hepatotoxicity after a two-day treatment with regular doses of acetaminophen. A nine-month-old female was referred because of intractable metabolic acidosis. She was given acetaminophen at therapeutic doses over a 48-hour period. She was hospitalized because of confusion and metabolic acidosis. Liver function tests were abnormal with normal bilirubin levels. The urine gas chromatography-mass spectrometry (GC/MS) showed massive excretion of 5-oxoproline. She improved and liver function tests normalized in the next six days, but compensated metabolic acidosis and massive 5-oxoprolinuria persisted. The analysis of GS in erythrocytes revealed 5% of normal enzyme activity, and the patient had 491G > A mutation on both alleles in the GS gene. In this report it can be assumed that patients, even if heterozygous for a mutation of the GS gene, are at risk for acetaminophen toxicity.
科研通智能强力驱动
Strongly Powered by AbleSci AI