Goebel H H, Zeman W, Pilz H
J Neurol. 1976 Oct 4;213(4):295-303. doi: 10.1007/BF00316269.
Specimens of brachial plexus, sural nerve and two cranial nerves of one patient with Jansky-Bielschowsky type and 3 patients with the Spielmeyer-Sjögren type of NCL were studied by electron microscopy. Significant light microscopic changes were absent in all specimens. Ultrastructurally, curvilinear and/or fingerprint inclusions were present in each case, located chiefly in Schwann cells. These diagnostic findings were, however, overshadowed by masses of lamellar pi-granule-like cytosomes, usually not mixed with curvilinear or finger-print profiles in the juvenile cases and only rarely associated with curvilinear profiles in the late infantile case. Since secondary changes of axons and myelin sheaths were mild, these lamellar cytosomes might indicate chronic damage to Schwann cells, perhaps by "wear and tear" as seen in aging as well as NCL. On account of the abundance of pi-granules in NCL, peripheral nerve biopsy appears less suitable for confirming this diagnosis than biopsy of skin, striated muscle and rectal tissue.
对1例患有扬斯基-比尔绍斯基型和3例患有施皮尔曼-舍格伦型神经元蜡样脂褐质沉积症(NCL)患者的臂丛神经、腓肠神经和两条颅神经标本进行了电子显微镜研究。所有标本在光学显微镜下均未发现明显变化。超微结构上,每例均存在曲线状和/或指纹状包涵体,主要位于施万细胞内。然而,这些诊断性发现被大量板层状π颗粒样胞质小体所掩盖,在青少年病例中,这些胞质小体通常不与曲线状或指纹状结构混合,而在晚期婴儿型病例中,仅很少与曲线状结构相关。由于轴突和髓鞘的继发性改变较轻,这些板层状胞质小体可能表明施万细胞受到慢性损伤,可能是如衰老以及NCL中所见的“磨损”所致。鉴于NCL中π颗粒丰富,与皮肤、横纹肌和直肠组织活检相比,周围神经活检似乎不太适合用于确诊该疾病。