Encefalopatía aguda asociada a anestesia general en un paciente adulto portador de la variante m.11232T>C en el gen MT-ND4

IF 1.3 Q3 ANESTHESIOLOGY
I. Arranz Chamorro, P. Blanco-Schweizer, E. Ruiz Pesini, M. Busto Busto, T. Ticona Espinoza, J. Rodríguez Jiménez
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引用次数: 0

Abstract

We report the case of a 20-year-old woman who developed acute encephalopathy after uneventful general anesthesia with sevoflurane, propofol, and opioids. The patient presented neurological impairment followed by metabolic acidosis and hyperlactatemia and neuroimaging findings involving the basal ganglia, brainstem, and cerebellum. Genetic testing confirmed the mitochondrial variant m.11232T>C in the MT-ND4 gene, previously described only in pediatric patients. This case could be one of the first cases described in the literature of acute encephalopathy associated with this mutation in an adult patient, possibly precipitated by exposure to volatile anesthetics. The patient's favorable clinical and radiological evolution after intensive neuroprotective management and suboccipital decompressive craniectomy highlights the importance of early diagnosis and individualized treatment. Mitochondrial dysfunction should be considered in atypical neurological presentations following general anesthesia, especially when accompanied by lactic acidosis and unusual neuroimaging findings.
携带MT-ND4变异m.11232T>C的成人患者伴有全身麻醉的急性脑病
我们报告一例20岁的女性在七氟醚、异丙酚和阿片类药物的全身麻醉后发生急性脑病。患者先是出现代谢性酸中毒和高乳酸血症后出现神经功能障碍,神经影像学发现涉及基底节区、脑干和小脑。基因检测证实了MT-ND4基因中的线粒体变异m.11232T>;C,以前只在儿科患者中发现。该病例可能是文献中首次描述的与成年患者的这种突变相关的急性脑病病例之一,可能是由于暴露于挥发性麻醉剂而引起的。患者在强化神经保护治疗和枕下减压颅骨切除术后良好的临床和影像学进展突出了早期诊断和个体化治疗的重要性。在全麻后的非典型神经表现中应考虑线粒体功能障碍,特别是当伴有乳酸酸中毒和异常的神经影像学发现时。
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来源期刊
CiteScore
1.80
自引率
15.40%
发文量
113
审稿时长
82 days
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