Slavin G, Wills E J, Richmond J E, Chanarin I, Andrews T, Stewart G
J Clin Pathol. 1975 Sep;28(9):701-10. doi: 10.1136/jcp.28.9.701.
The morphological changes in a patient with a generalized storage disease characterized by the intracellular deposition of neutral lipid are described. There is widespread accumulation of lipid in the cytoplasm of many cells and in occasional nuclei. Diagnosis may be facilitated by the recognition of clear vacuoles in the cytoplasm of granulocytes in blood films. In jejunal biopsies vacuolation of the epithelial cells may simulate the appearances of a-betalipoproteinaemia. The lipid inclusions consist largely of normal triglycerides and are free in the cytoplasm, unassociated with any organelle. The biochemical basis of the lesions is uncertain. Although there are lipoprotein abnormalities the primary defect appears to be intrinsic to the cell and may involve either a defective cytoplasmic lipase or an impaired uptake and utilization of fatty acids by mitochondria.
本文描述了一名患有以中性脂质细胞内沉积为特征的全身性贮积病患者的形态学变化。许多细胞的细胞质以及偶尔的细胞核中都有广泛的脂质蓄积。通过识别血片中粒细胞细胞质中的清亮空泡,有助于诊断。在空肠活检中,上皮细胞的空泡化可能类似无β脂蛋白血症的表现。脂质包涵体主要由正常甘油三酯组成,在细胞质中呈游离状态,不与任何细胞器相关联。这些病变的生化基础尚不确定。虽然存在脂蛋白异常,但主要缺陷似乎是细胞固有的,可能涉及细胞质脂肪酶缺陷或线粒体对脂肪酸的摄取和利用受损。