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An electron microscope study of the glomerulus in nephrosis, glomerulonephritis, and lupus erythematosus

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TLDR
Renal biopsies from 16 patients with nephrosis, 7 patients with glomerulonephritis, and 3 patients with disseminated lupus erythematosus were studied with the electron microscope to indicate that early in the course of each of these diseases alterations occur in the fine structure of the glomeruli which serve to distinguish one disease process from another.
Abstract
Renal biopsies from 16 patients with nephrosis, 7 patients with glomerulonephritis, and 3 patients with disseminated lupus erythematosus were studied with the electron microscope. The observations presented indicate that early in the course of each of these diseases alterations occur in the fine structure of the glomeruli which serve to distinguish one disease process from another. In nephrosis, some distortion of the organization of the epithelial foot processes was seen in all patients. These epithelial changes constituted the early, consistent lesion of the disease. There was frequently also a swelling of the endothelium. In glomerulonephritis, pronounced proliferative changes involving the endothelium and to a lesser extent the epithelium, together with the laying down of a basement membrane-like material, represented the predominate pathologic processes. There was also a swelling of both endothelial and epithelial cytoplasm. The epithelial foot processes generally appeared normal. In patients with a clinically "mixed" picture of nephrosis and nephritis, the glomerular changes were likewise "mixed," for various combinations of epithelial, endothelial, and basement membrane abnormalities were present. In disseminated lupus erythematosus, a more or less generalized thickening of the basement membrane proper associated with a variable degree of endothelial proliferation was seen. It is suggested that an accentuation of the process of basement membrane thickening results in the "wire loop" appearance sometimes seen by light microscopy. Although the earliest alterations in glomerular fine structure were characteristic for each of the disease processes, at later stages the changes were not always distinctive. The resulting scarred or "hyalinized" glomeruli, composed of relatively homogeneous, basement membrane-like material, and a few atrophic cells, appeared quite similar. Although the functional implications of the structural changes observed remain obscure at this time, it is believed that insight into mechanisms may stem from such observations.

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Citations
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The podocyte's response to injury: Role in proteinuria and glomerulosclerosis

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Pathology of the nephrotic syndrome in children: a report for the International Study of Kidney Disease in Children.

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FUNCTIONAL EVIDENCE FOR THE EXISTENCE OF A THIRD CELL TYPE IN THE RENAL GLOMERULUS : Phagocytosis of Filtration Residues by a Distinctive "Third" Cell

TL;DR: Experiments carried out with electron-opaque tracers indicated that a functional distinction, based on extent of phagocytosis, can be made between the superficial and deep cells, thus supporting the existence of a distinctive "third" cell (in addition to endothelium and epithelium) in the renal glomerulus.
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Cyclical edema and shock due to increased capillary permeability.

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References
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Journal ArticleDOI

A study of fixation for electron microscopy

TL;DR: Fixation experiments with buffered OsO4 solutions have shown that the appearance of the fixed cells is conditioned by the pH of the fixative, and the quality of fixation can be materially improved by buffering the OsO 4 solutions at pH 7.3-7.5 with acetate-veronal buffer.
Journal ArticleDOI

The fine structure of the renal glomerulus of the mouse

TL;DR: Sections of mouse renal glomerulus fixed by perfusion with buffered osmium tetroxide solution have been studied with the electron microscope and the description of Zimmermann (54), based on a light microscope study, is confirmed in many respects.
Journal ArticleDOI

Ultra-microtomy by a new method.

TL;DR: Polymerization of n-butyl methacrylate monomer is used as a rapid and simple means for embedding fixed biological material and provides an optically clear matrix for cutting very thin sections, one at a time, with a slightly modified conventional rotary microtome.
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