Key result
Neutral lipid storage disease exhibits widespread intracellular accumulation of normal triglycerides unassociated with organelles.
Why the study?
The morphological changes and biochemical basis of a generalized neutral lipid storage disease characterized by intracellular lipid deposition are not well understood.
Case Report (n=1)
Describes the morphological features of a neutral lipid storage disease, highlighting widespread cytoplasmic lipid accumulation and diagnostic clues in blood films and jejunal biopsies.
May aid pathologic diagnosis via blood films and biopsies; hypothesis-generating for pathogenesis in neutral lipid storage disease.
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.
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Slavin et al. (1975) conducted a case report in Neutral lipid storage disease (n=1). Morphological evaluation of a patient with neutral lipid storage disease revealed widespread intracellular accumulation of normal triglycerides unassociated with any organelle.
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