病理
组织细胞
神经元蜡样脂褐素沉着症
超微结构
骨髓
医学
活检
染色
解剖
疾病
作者
Charles E. Miley,Gilbert S. Omenn,Thomas D. France,John F. O’Brien,Raymond W. M. Chun
出处
期刊:Neurology
[Lippincott Williams & Wilkins]
日期:1978-10-01
卷期号:28 (10): 1008-1008
被引量:23
标识
DOI:10.1212/wnl.28.10.1008
摘要
Neuronal ceroid-lipofuscinosis is manifested by visual and intellectual deterioration and seizures. Autofluorescent lipopigments are found in neural and many nonneural tissues, with characteristic staining and ultrastructural properties. Presumptive diagnosis can usually be made on the basis of history, physical examination, and electrodiagnostic tests, but in the absence of a specific biochemical defect, histologic confirmation is essential. A 6-year-old boy with the clinical appearance of the juvenile form of the disease had sea-blue histiocytes in the bone marrow. And curvilinear profiles in ultrastructural inclusions in skin biopsy tissue, cultures skin fibroblasts, and bone marrow cells.
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