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Brain magnetic resonance imaging and proton MR spectroscopic findings after metabolic crisis in 3-methylcrotonylglycinuria

机译:3-甲基巴豆酰甘氨酸尿症代谢危机后的脑磁共振成像和质子MR光谱发现

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摘要

Magnetic resonance imaging (MRI) and magnetic resonance spectroscopic (MRS) findings in 3-methylcrotonylglycinuria presenting with acute metabolic decompensation in a previously healthy 7-year-old female are described. The patient was hospitalized with fever, irritability, gastrointestinal problems, drowsiness, signs of upper motor neuron deficit, and rapidly progressive respiratory distress requiring assisted ventilation. Laboratory workup showed severe metabolic acidosis, and the diagnosis of 3-methylcrotonylglycinuria was established by the mass spectrometry analysis of urine sample. Although initial CT imaging workup was found to be gross normal, subsequent MRI of the brain in the early chronic stage of the disease showed symmetrical ill-defined signal abnormalities within medulla oblongata, pons, inferior cerebellar peduncles, and periventricular white matter in cerebral hemispheres. Diffusion-weighted images were unremarkable. Single-voxel proton MRS showed elevated levels of lactate, branched-chain amino acids, as well as glutamine and glutamate. To the best of our knowledge, this is the first reported case of late onset 3-methylcrotonylglycinuria with complete MRI and MRS workup in the early chronic phase after metabolic crisis.
机译:描述了在先前健康的7岁女性中出现急性代谢失代偿的3-甲基巴豆酰糖尿症的磁共振成像(MRI)和磁共振波谱(MRS)发现。该患者因发烧,易怒,胃肠道问题,嗜睡,上运动神经元缺陷的体征以及需要辅助通气的快速进行性呼吸窘迫住院。实验室检查显示严重的代谢性酸中毒,并通过尿液样品的质谱分析确定了3-甲基巴豆酰甘氨酸尿症的诊断。尽管发现最初的CT影像检查总体正常,但在疾病早期慢性阶段的后续脑部MRI显示在延髓,脑桥,小脑小脑梗和脑半球室周白质内出现对称的,信号模糊的信号异常。弥散加权图像不明显。单体素质子MRS显示乳酸,支链氨基酸以及谷氨酰胺和谷氨酸水平升高。据我们所知,这是首例报告的晚期3-甲基巴豆酰甘露尿症,在代谢危象后的慢性早期阶段完成了MRI和MRS检查。

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