[Later onset metachromatic leukodystrophy diagnosed by nerve biopsy].

J X Zhao
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引用次数: 0

Abstract

Three cases of later onset metachromatic leukodystrophy in one family were reported. The brother is 32 years old, younger sister is 35 years old and the elder sister is 39 years old, who were normal as child without any family history of neurological disease. The three cases began their illness at about the age of 30 years old with dysarthria, progressive dementia, motor disturbance and numbness in the extremities. CT scan showed low density in the white matter of frontal, parietal lobes and around the ventricle. The written reports of CT scan were lacunar infarction in brother, multiple lacunar infarction in younger sister and Binswanger's disease in elder sister. Nerve biopsy showed myelinated fibers were decreased in number. Metachromatical materials were seen in and around the Schwann cell cytoplasm. Metachromatical materials were lamillar inclusions in granular matrix by electromicroscopic examination. So nerve biopsy is easy, safe and effective method to diagnose the uncertain pathogenic leukoence-phalopathy.

[神经活检诊断后发性异色性脑白质营养不良]。
本文报道1个家族中3例晚发性异色性脑白质营养不良。兄弟32岁,妹妹35岁,姐姐39岁,幼年正常,无神经系统疾病家族史。这三例患者大约在30岁时发病,伴有构音障碍、进行性痴呆、运动障碍和四肢麻木。CT示额、顶叶及脑室周围白质低密度。CT扫描的书面报告为弟弟腔隙性梗死,妹妹多发腔隙性梗死,姐姐Binswanger病。神经活检显示髓鞘纤维数量减少。雪旺氏细胞质内及周围可见异色物质。差色材料为颗粒状基体中的层状夹杂物。因此,神经活检是一种简便、安全、有效的诊断不明致病性白质指病的方法。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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