Brismar J, Aqeel A, Brismar G, Coates R, Gascon G, Ozand P
Department of Radiology, King Faisal Specialist Hospital and Research Center, Riyadh, Saudi Arabia.
AJNR Am J Neuroradiol. 1990 Nov-Dec;11(6):1219-28.
Ten infants with classical maple syrup urine disease (MSUD) and two with variant MSUD had a total of 26 CT scans and 13 MR examinations of the brain during different stages of their disease. We found that inter- and intrapatient analyses of CT and MR findings at times ranging from 3 days to 7 months were typical enough to suggest the MSUD diagnosis. Imaging studies showed the natural course of the disease and, in a few cases, illustrated the effects of therapy. CT scans typically are negative during the first few days of life, then a marked, generalized, diffuse edema appears. In addition, a localized, more severe edema (the MSUD edema) is seen, which involves the deep cerebellar white matter, the dorsal part of the brainstem, the cerebral peduncles, and the dorsal limb of the internal capsule. Both the generalized and the MSUD edema subside during the second month of life, then may disappear totally or leave a well-defined, low-density zone around the lateral ventricles and small, low-attenuation lesions within the brainstem, respectively. With the disappearance of the edema, some loss of brain substance becomes obvious.
10例患有典型枫糖尿症(MSUD)的婴儿和2例患有变异型MSUD的婴儿在疾病的不同阶段共进行了26次脑部CT扫描和13次脑部磁共振成像(MR)检查。我们发现,在出生3天至7个月的不同时间点对CT和MR检查结果进行患者间和患者内分析,其特征足以提示MSUD的诊断。影像学研究显示了疾病的自然病程,在少数情况下,还说明了治疗效果。CT扫描在出生后的头几天通常为阴性,随后会出现明显的、全身性的弥漫性水肿。此外,还可见局限性的、更严重的水肿(MSUD水肿),累及小脑深部白质、脑干背侧、大脑脚和内囊后肢。全身性水肿和MSUD水肿在出生后第二个月会消退,随后可能完全消失,或分别在侧脑室周围留下边界清晰的低密度区以及脑干内的小低密度病变。随着水肿的消失,一些脑实质的损失变得明显。