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Glomerulonephritis[1] belongs to glomerulopathies. It is a disease of the glomeruli, which has an inflammatory nature and is conditioned by immunological processes. Glomerulonephritis can be divided into primary (where only the kidneys are affected) and secondary, when kidney involvement is part of another systemic disease (for example, systemic lupus erythematosus).

Classification of glomerulonephritis[edit | edit source]

The classification of glomerulonephritis (GN) is complicated and not completely complete yet. There are several criteria according to which individual pathological units can be classified.

Membranoproliferative glomerulonephritis
Membranous nephropathy
Diabetic nephropathy
ANCA positive glomerulonephritis.

Division according to time perspective[edit | edit source]

  1. Acute glomerulonephritis
  2. Subacute glomerulonephritis
  3. Chronic glomerulonephritis

Division according to etiology[edit | edit source]

1. Primary glomerulonephritis - or also idiopathic. We do not know the exact cause. The disease is only related to the kidneys.

2. Secondary glomerulonephritis - a disease in which we know the triggering process, the kidneys are affected as part of another systemic disease.

Division according to the nature of the manifestation in primary GN[edit | edit source]

1. Proliferative glomerulonephritis - characterized by clearly expressed inflammatory events. Clinical signs: more pronounced cell proliferation, with positive immunofluorescence, mixed findings in the urine. They are more often manifested by nephritic syndrome.

2. Nonproliferative glomerulonephritis - characterized by a low degree of inflammation. Clinical signs: without cell proliferation, with negative immunofluorescence, proteinuria in the urine. They are also most often manifested by nephrotic syndrome.

Rapidly progressive glomerulonephritis[edit | edit source]

This is a form of glomerulonephritis that causes deterioration of renal function over days or weeks. Histologically, it is a sickle-shaped form of GN, where the sickles affect at least 75% of the glomeruli. Most often, the following units take place under this image:

  1. ANCA associated renal vasculitis - antibodies against neutrophil cytoplasm (Granulomatosis with polyangiitis, Microscopic polyangiitis, Churg-Strauss syndrome )
  2. Anti-GBM antirenal glomerulonephritis - basement membrane antibodies (Goodpasture syndrome)
  3. Immunocomplex glomerulonephritis - deposits of immune complexes (SLE, poststreptococcal glomerulonephritis, IgA nephropathy)

Links[edit | edit source]

Related Articles[edit | edit source]

External links[edit | edit source]

Literature[edit | edit source]

  • KUMAR, Vinay – ABBAS, Abul K – FAUSTO, Nelson. Robbins basic pathology. 8. edition. Philadelphia : Saunders/Elsevier, 2007. ISBN 978-1-4160-2973-1.

  • CZECH, Richard. Intern. 1. edition. Prague : Triton, 2010. 855 pp. ISBN 978-80-7387-423-0.

References[edit | edit source]

  1. KLENER, Paul. Internal Medicine. Third, revised and supplemented edition edition. Prague : Karolinum, Galen, 2006. 1158 pp. pp. 739–740. ISBN 80-7262-430-X.