Xiao B
Department of Neurology, First Affiliated Hospital, Hunan Medical University, Changsha.
Zhonghua Shen Jing Jing Shen Ke Za Zhi. 1992 Oct;25(5):278-80, 316.
4 unrelated patients with infantile type (one case), late infantile type (one case), juvenile type (two case) of neuronal ceroid-lipofuscinosis were reported. The pathological study by brain biopsy was carried out with light and electron microscopes as well as histochemical methods. Ultrastructurally, the infantile type showed deposits of lipofuscin bodies, fingerprint bodies, and the late infantile type showed a lot of curvilinear bodies and paracrystalline bodies. The ultrastructural configuration in the juvenile type is more heterogeneous and consisted of combination of lipofuscin bodies, fingerprint bodies and multilamellar structures. It was emphasized that fingerprint bodies were first discovered in infantile type, which might challenge the view that only lipofuscin bodies can be found in infantile type.
报道了4例神经元蜡样脂褐质沉积症的无关患者,其中婴儿型1例、晚婴儿型1例、少年型2例。通过脑活检进行了光镜、电镜及组织化学方法的病理研究。超微结构上,婴儿型可见脂褐质小体、指纹体沉积,晚婴儿型可见大量曲线体和副晶体。少年型的超微结构形态更为多样,由脂褐质小体、指纹体和多层结构组合而成。强调指纹体首次在婴儿型中发现,这可能挑战了婴儿型仅能发现脂褐质小体的观点。