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佩利措伊斯-梅茨巴赫病的计算机断层扫描

Computed tomography in Pelizaeus-Merzbacher disease.

作者信息

Statz A, Boltshauser E, Schinzel A, Spiess H

出版信息

Neuroradiology. 1981;22(2):103-5. doi: 10.1007/BF00344782.

Abstract

CT findings in two related males suffering from the classical X-linked recessive form of Pelizaeus-Merzbacher disease (PMD) are described. CT revealed marked cerebellar atrophy and focal areas of demyelination of cerebral white matter in a 25-year-old patient. This agrees with known neuropathological changes. However, CT was normal in the 14-year-old nephew, although his neurological symptoms were nearly as severe as his uncle's. Judging from this observation and from the scant information in the literature it seems that CT in classical PMD is normal in the first decade and is therefore not helpful in confirming the diagnosis of PMD at an early stage.

摘要

本文描述了两名患有典型X连锁隐性型佩利措伊斯-梅茨巴赫病(PMD)的相关男性患者的CT检查结果。CT显示,一名25岁患者出现明显的小脑萎缩和脑白质脱髓鞘灶。这与已知的神经病理学变化相符。然而,尽管14岁侄子的神经症状几乎与他叔叔的一样严重,但其CT检查结果正常。根据这一观察结果以及文献中的少量信息来看,典型PMD患者在第一个十年的CT检查结果似乎是正常的,因此在疾病早期对确诊PMD并无帮助。

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