Argyrakis A, Pilz H, Goebel H H, Müller D
J Neuropathol Exp Neurol. 1977 Jul;36(4):693-711. doi: 10.1097/00005072-197707000-00005.
In a 13-year-old neurologically healthy boy from a family with adult-onset of metachromatic leukodystrophy (MLD) showing arylsulfatase A-deficiency in the adult, sural nerve biopsy probably was performed 2-3 decades before clinical manifestation of the disease could be expected. Ultrastructurally 4 basic types of inclusion bodies in Schwann cells could be demonstrated (pleo-morphic "zebra body"-like inclusions, double-lamellated inclusions, "tuff-stone"-like inclusions, granular osmiophilic inclusions). Additionally, endoplasmatic reticulum, mitochondria and lysosomes showed marked alterations. Advanced damage of myelin was only rarely seen, but initial segmental demyelination was a common finding. These early pathological changes in chronic MLD are thought to represent a subcellular metabolic insufficiency of Schwann cells in this disease.
一名13岁的神经功能正常男孩来自一个成年发病的异染性脑白质营养不良(MLD)家族,该家族中的成年人显示芳基硫酸酯酶A缺乏。腓肠神经活检可能在预计疾病临床表现出现前2至3十年进行。超微结构上可显示施万细胞中4种基本类型的包涵体(多形性“斑马体”样包涵体、双板层包涵体、“凝灰岩样”包涵体、嗜锇颗粒包涵体)。此外,内质网、线粒体和溶酶体显示出明显改变。髓鞘的严重损伤很少见,但初始节段性脱髓鞘是常见发现。慢性MLD中的这些早期病理变化被认为代表了该疾病中施万细胞的亚细胞代谢不足。