Taccone A, Tortori Donati P, Marzoli A, Dell'Acqua A, Gatti R, Leone D
Department of Radiology, G. Gaslini Institute, Genoa, Italy.
Pediatr Radiol. 1993;23(5):349-52. doi: 10.1007/BF02011954.
Cranial CT and/or MRI imaging of 8 patients with mucopolysaccharidosis (MPS) was retrospectively evaluated. Two patients had MPS IH, 1 had MPS IS, 1 had MPS IVA and 4 had MPS IV. CT and MRI showed thickening of dura mater at the cranio-cervical junction, causing narrowing of the subarachnoid space, in all the patients examined. Spinal cord compression was detected in 4 patients. Other findings were: white matter alterations, mild to severe hydrocephalus, skull dysplasia and odontoid dysplasia. White matter alterations were evident as large areas and as multiple dispersed spots of prolonged T1 and T2 value. Reduced gray/white matter contrast was demonstrated on T2-weighted MRI images. It is important to examine the cranio-cervical junction carefully for thickening of dura mater in all patients with mucopolysaccharidosis examined by CT or MRI, because of the generally progressive clinical course of MPS. In patients with symptomatic cord compression, surgical intervention should be considered.
对8例黏多糖贮积症(MPS)患者的头颅CT和/或MRI成像进行了回顾性评估。其中2例为MPS IH型,1例为MPS IS型,1例为MPS IVA型,4例为MPS IV型。CT和MRI显示,所有接受检查的患者在颅颈交界处硬脑膜增厚,导致蛛网膜下腔狭窄。4例患者检测到脊髓受压。其他表现包括:白质改变、轻至重度脑积水、颅骨发育异常和齿状突发育异常。白质改变表现为大面积以及多个散在的T1和T2值延长的斑点。T2加权MRI图像显示灰质/白质对比度降低。由于MPS通常呈进行性临床病程,因此对于所有接受CT或MRI检查的黏多糖贮积症患者,仔细检查颅颈交界处硬脑膜增厚情况很重要。对于有症状性脊髓受压的患者,应考虑手术干预。