苯酚中毒的血管内溶血:一种未预见的罕见并发症

Archi Sharma, Giorgi Saikia
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引用次数: 0

摘要

黑苯基是一种强大的杀菌剂,用于家庭和医院,很容易获得,可以带着自残的意图食用。经吸入或溢出引起的血管内溶血已有报道,但经摄入引起的血管内溶血很少报道。一名25岁的健康男性在摄入黑苯基后就诊,就诊时无症状。第4天,患者出现发热、黄疸、心动过速、乏力、尿呈深褐色。实验室Hgb 3.6g/dl,血小板计数27.5万/ul,肌酐1.1mg/ dI, AST 244U/L, ALT 69U/L,总胆红素4.65g/dl(间接3.35)PT 14.6, INR 1.23。第6天,尿颜色变暗,提示正在进行溶血,LDH水平为3614 U/L。在整个住院期间,尿量维持正常,他没有出现急性肾损伤。第9天,患者症状好转,第12天出院。这些化合物干扰细胞中的氧化磷酸化,使红细胞失去渗透平衡。这种代谢障碍可能导致红细胞过早溶解。虽然入院时无症状,但患者在第4天出现严重的血管内溶血和血红蛋白尿。这表明需要入院无症状患者,持续监测和预测化合物的毒性潜力。由于缺乏关于这种罕见并发症的足够文献,我们报告了印度东北部的第一例病例。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Intravascular hemolysis in phenol poisoning: An unforeseen and rare complication
The black phenyl is a powerful germ killer used for homes, hospitals, which is easily accessible and can be consumed with the intention of self harm. Cases of intravascular hemolysis through inhalation or spillage has been reported, but intravascular hemolysis following ingestion is rarely reported. A 25 year old previously healthy male presented after alleged ingestion of black phenyl and was asymptomatic at presentation. By day 4, he developed fever, icterus, tachycardia, fatigue and dark brown urine. Labs were Hgb 3.6g/dl, platelet count 2.75 lakhs/ul, creatinine 1.1mg/ dI, AST 244U/L, ALT 69U/L, Total Bilirubin 4.65g/dl (Indirect 3.35) PT 14.6, INR 1.23. By Day 6, urine color darkened, suggestive of ongoing hemolysis with LDH level of 3614 U/L. Over the full hospital stay, urine output was maintained, and he didn't develop acute kidney injury. By Day 9, patient's symptoms improved & he was discharged on day 12. These compounds interfere with oxidative phosphorylation in cells, making red blood cells losing osmotic equilibrium. This metabolic handicap may lead to premature red blood cell lysis. Though asymptomatic at presentation, patient developed serious intravascular hemolysis and hemoglobinuria by day 4. This suggests the need for admission of asymptomatic patients, constant monitoring and to anticipate toxic potentials of the compound. The dearth of enough literature on this rare complication made us report this first case from North East India.
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