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Early glomerular lesions in amyloidosis. Electronmicroscopic findings

Virchows Archiv. A, Pathological Anatomy and Histology
|January 1, 1981
PubMed

Insights

Early renal amyloidosis involves glomerular amyloid deposits in the mesangium and capillary walls. These deposits originate from blood-borne precursors, with local enzymes potentially aiding fibril formation within the glomerulus.

Area of Science:

  • Nephrology
  • Pathology
  • Cell Biology

Background:

  • Renal amyloidosis is characterized by amyloid deposition in kidney tissues.
  • Understanding early glomerular changes is crucial for diagnosing and managing renal amyloidosis.

Purpose of the Study:

  • To investigate the initial morphological alterations in glomeruli during renal amyloidosis.
  • To elucidate the origin and formation process of amyloid within the glomerulus.

Main Methods:

  • Analysis of renal biopsies using light and electron microscopy.
  • Morphological examination of mesangial, epithelial, and endothelial cells.

Main Results:

  • Amyloid deposits were observed predominantly in the mesangial matrix, extending into subepithelial spaces.
  • In some cases, deposits were found in both mesangium and capillary walls, seemingly independent.
  • Morphological changes suggested intracellular processing of amyloid precursors within glomerular cells.

Conclusions:

  • Amyloid in the glomerulus originates from circulating amyloid precursors.
  • Local glomerular cells, via lysosomal enzymes, may contribute to amyloid fibril formation extracellularly.

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