al-Moutaery K R, Choudhury A R, Hassanen M O
Department of Neurosurgery, Riyadh Armed Forces Hospital, Kingdom of Saudi Arabia.
Acta Neurochir (Wien). 1994;131(1-2):160-3. doi: 10.1007/BF01401468.
We report a 2.5-year-old boy with Saudi variant of multiple sulfatase deficiency (MSD or Austin's disease). He presented with the features of cervical cord compression and a severe form of hydrocephalus. The former was due to a thickened posterior arch of the atlas and the latter from a narrow foramen magnum and meningeal thickening. Decompression of the cord was achieved by removal of the posterior margin of the foramen magnum and posterior arch of the atlas, and followed by a duroplasty. At a later date, ventricular decompression was achieved by insertion of a ventricular-peritoneal shunt. NMR did not demonstrate white matter changes in the brain. In this regard the reported case differs from the earlier description of the Saudi Variant of MSD.
我们报告了一名2.5岁患有沙特型多种硫酸酯酶缺乏症(MSD或奥斯汀病)的男孩。他表现出颈髓受压和严重脑积水的特征。前者是由于寰椎后弓增厚,后者是由于枕骨大孔狭窄和脑膜增厚。通过切除枕骨大孔后缘和寰椎后弓实现脊髓减压,随后进行硬脑膜成形术。之后,通过插入脑室-腹腔分流管实现脑室减压。核磁共振成像未显示脑部白质改变。在这方面,该报告病例与MSD沙特型的早期描述不同。