From the Departments of Pediatric Radiology (A.A.N., M.A., M.E.-B.)
Pediatric Neurology (J.D., F.R., M.S.), Robert Debré University Hospital, Assistance Publique-Hôpitaux de Paris, Paris, France.
AJNR Am J Neuroradiol. 2021 Sep;42(9):1722-1726. doi: 10.3174/ajnr.A7199. Epub 2021 Jul 8.
Patients with glutaric aciduria type 1, without early diagnosis and initiation of preventive treatment, often develop movement disorders and various degrees of motor disability due to striatal area-specific damage induced by an acute episode of metabolic decompensation. The neuroimaging phenotype of patients with glutaric aciduria type 1 includes characteristic cyst-like bilateral enlargement of the Sylvian fissures and anterior subarachnoid spaces and signal abnormalities including supratentorial white matter and deep gray matter structure T2 hyperintensities, frequently associated with restricted diffusion. In this retrospective study, we add to the neuroimaging spectrum of glutaric aciduria type 1, a novel imaging finding present regardless of a previous metabolic crisis: the enlargement of the optic chiasm associated with signal abnormalities in the anterior intracranial visual structures observed in 6 of 10 patients. These optic pathway abnormalities are suggested as useful diagnostic clues for glutaric aciduria type 1, and possible pathophysiologic mechanisms are discussed.
1 型戊二酸尿症患者若未能早期诊断和启动预防治疗,往往会因代谢失代偿急性发作导致纹状体区域特异性损伤而出现运动障碍和不同程度的运动功能障碍。1 型戊二酸尿症患者的神经影像学表型包括特征性的、双侧、囊肿样的大脑外侧裂和前蛛网膜下腔扩大,以及包括幕上脑白质和深部灰质结构 T2 高信号等信号异常,常伴有弥散受限。在这项回顾性研究中,我们增加了 1 型戊二酸尿症的神经影像学谱,提出了一种新的影像学发现,无论之前是否存在代谢危象:10 例患者中有 6 例出现视交叉扩大,并伴有前颅内视觉结构的信号异常。这些视路异常可作为 1 型戊二酸尿症的有用诊断线索,同时探讨了可能的病理生理机制。