一个有呼吸困难和巧克力棕色动脉血的孩子

Fanny Amalraj, P. Jose, S. Ponnarmeni, Peter Prasanth Kumar Kommu
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引用次数: 0

摘要

高铁血红蛋白血症是当血红素被氧化时发生的一种血红蛋白病。氧化血红素中的铁不能结合和运输氧。因此,当浓度超过15%时,症状开始为发绀、窘迫和呼吸急促,随着浓度的增加,可能发展为癫痫发作、意识不清甚至死亡。先天性高铁血红蛋白血症是罕见的,临床上经常被遗漏,但药物治疗效果良好。在此,我们报告一名十二岁女孩,呼吸窘迫而无紫绀。诊断是基于巧克力棕色的动脉血液样本进行分析。在病因不明的呼吸窘迫病例中,考虑这种情况作为鉴别诊断的重要性正在这里讨论。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
A child with respiratory distress and chocolate brown arterial blood
Methemoglobinemia is a hemoglobinopathy that occurs when the heme is oxidated. Ferric iron in oxidized heme cannot bind and transport oxygen. Hence, when the concentration exceeds 15%, symptoms start with cyanosis, distress, and tachypnea, and may progress to seizure, unconsciousness, and even death as the concentration increases. Congenital methemoglobinemia is rare and often clinically missed but responds well with medications. Here, the case of a 12-year-old girl with respiratory distress and no cyanosis is being reported. The diagnosis was made based on a chocolate brown-colored arterial blood sample taken for analysis. The importance of considering this condition as a differential diagnosis in a case of respiratory distress of unknown etiology is being discussed here.
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