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. 2002;74(6):31-3.

[Nephrotic syndrome in minimal change disease (kidney), focal segmental glomerulosclerosis, and focal mesangioproliferative glomerulonephritis]

[Article in Russian]
  • PMID: 12136479

[Nephrotic syndrome in minimal change disease (kidney), focal segmental glomerulosclerosis, and focal mesangioproliferative glomerulonephritis]

[Article in Russian]
T S Voznesenskaia et al. Ter Arkh. 2002.

Abstract

Aim: To specify clinical and laboratory characteristics of minimal change disease (MCD), focal mesangioproliferative glomerulonephritis (MPGN), focal-segmental glomerulosclerosis (FSGS).

Material and methods: A retrospective analysis of 45 case histories of children (renal biopsy for nephrotic syndrome) has shown that morphologically 13 of them had MCD, 15--FSGS and 17--focal MPGN. Clinical, laboratory, immunofluorescent and electron microscopy findings typical for each of the morphological types were studied.

Results: The data obtained suggest that MCD, FSGS and focal MPGN may represent independent forms of glomerulonephritis.

Conclusion: If a differential diagnosis by renal biopsy is difficult, information from the disease history and clinico-laboratory evidence should be used.

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