van der Knaap M S, Jakobs C, Valk J
Department of Pediatrics, Free University Hospital, Amsterdam, The Netherlands.
J Inherit Metab Dis. 1996;19(4):535-47. doi: 10.1007/BF01799114.
Mitochondrial defects, defects in gluconeogenesis, and biotin-responsive multiple carboxylase deficiency are disorders characterized by primary lactic acidosis. In this review, characteristic findings in magnetic resonance imaging (MRI) of the brain, as related to histopathological abnormalities, are described for the different disorders and the diagnostic value of the MRI findings is discussed. Inborn errors of metabolism with primary lactic acidosis should be considered in particular when MRI shows lesions similar to or reminiscent of effects of focal or generalized hypoxia-ischaemia, or when MRI shows signs of chronic neurodegeneration, but rarely in cases with predominantly white-matter changes.
线粒体缺陷、糖异生缺陷和生物素反应性多种羧化酶缺乏症是以原发性乳酸性酸中毒为特征的疾病。在本综述中,描述了与组织病理学异常相关的脑磁共振成像(MRI)的特征性表现,涉及不同疾病,并讨论了MRI表现的诊断价值。当MRI显示类似于或让人联想到局灶性或全身性缺氧缺血影响的病变时,或者当MRI显示慢性神经退行性变的迹象时,尤其应考虑原发性乳酸性酸中毒的先天性代谢缺陷,但在以白质改变为主的病例中很少见。