Taccone A, Tortori Donati P, Marzoli A, Dell'Acqua A, Occhi M, Gatti R, Leone D
Servizio di Radiologia, Istituto G. Gaslini, Genova.
Radiol Med. 1992 Sep;84(3):236-41.
Cranial CT and/or MRI examinations were performed in 8 patients affected with mucopolysaccharidosis. Two patients were affected with mucopolysaccharidosis IH,1 had mucopolysaccharidosis IS, 1 had mucopolysaccharidosis IV A and 4 presented mucopolysaccharidosis VI. CT and MRI showed white matter changes consisting of symmetric and diffuse hypodense areas on CT, large areas and multiple spots of prolonged T1 and T2 value on MRI. Reduced gray/white matter contrast was demonstrated on T2-weighted sequences. Furthermore, CT and MRI showed thickening of the dura mater at the cranio-cervical junction, which caused subarachnoid space narrowing in all patients. Spinal cord compression was detected in 4 patients. Additional findings were mild to severe hydrocephalus, skull dysplasia and odontoid dysplasia. Owing to the progressive clinical course of all mucopolysaccharidosis, the authors stress the importance of a careful study of the cranio-cervical junction in all the patients with mucopolysaccharidosis examined by CT or MRI in order to demonstrate essential thickening of the dura mater. In the patients with symptomatic cord compression, surgery should be considered.
对8例黏多糖贮积症患者进行了头颅CT和/或MRI检查。其中2例为黏多糖贮积症ⅠH型,1例为黏多糖贮积症ⅠS型,1例为黏多糖贮积症ⅣA型,4例为黏多糖贮积症Ⅵ型。CT和MRI显示白质改变,CT表现为对称弥漫性低密度区,MRI表现为大片及多发T1和T2值延长的斑点状影。T2加权序列显示灰白质对比度降低。此外,CT和MRI显示颅颈交界处硬脑膜增厚,所有患者均出现蛛网膜下腔狭窄。4例患者检测到脊髓受压。其他表现包括轻至重度脑积水、颅骨发育异常和齿状突发育异常。由于所有黏多糖贮积症的临床病程呈进行性,作者强调,对于所有接受CT或MRI检查的黏多糖贮积症患者,仔细研究颅颈交界处以发现硬脑膜增厚至关重要。对于有症状性脊髓受压的患者,应考虑手术治疗。