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Je něco špatně v tomto záznamu ?
Does electron microscopy change the view of the diagnosis of IgA nephropathy?
D Maixnerova, E Honsova, M Merta, J Reiterova, R Rysava, V Tesar, H Obeidova, J Motan
Jazyk angličtina Země Česko
Typ dokumentu práce podpořená grantem
Grantová podpora
NK7733
MZ0
CEP - Centrální evidence projektů
- MeSH
- biopsie MeSH
- elektronová mikroskopie MeSH
- IgA nefropatie diagnóza patologie MeSH
- ledviny * patologie MeSH
- lidé MeSH
- lipoidní nefróza diagnóza patologie MeSH
- Check Tag
- lidé MeSH
- Publikační typ
- práce podpořená grantem MeSH
Our study is aimed to reveal the frequency and clinical significance of the coincidence of two widely spread entities, e.g. minimal change disease (MCD) and IgA nephropathy (IgAN), claimed to be found in an overwhelming number in some Asian regions. We retrospectively analyzed clinical and histological data from 627 renal biopsies, performed in our department from January 2002 to January 2005 and completed electron microscopy in 112 specimens diagnosed as IgAN. The coincidence of IgAN and MCD was found in 8 patients (7.1%). The coincidence of IgAN and minimal change nephrotic syndrome (MCNS) clinically--especially presence of nephrotic syndrome and the response to drug therapy (with corticosteroids)--behaves as "pure" MCN. Our data from Czech Republic seem to suggest that the combination of IgAN with MCNS can be found relatively frequently not only in Asian patients (as stressed by some authors of Asian origin) but also in European inhabitants. The pathogenesis of the coincidence of IgAN and MCD needs to be elucidated by further studies.
Department of Nephrology 1st Faculty of Medicine Charles University Prague Czech Republic
Institute of Clinical and Experimental Medicine Prague Czech Republic
Obsahuje tabulky
Bibliografie atd.Literatura
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- $a Our study is aimed to reveal the frequency and clinical significance of the coincidence of two widely spread entities, e.g. minimal change disease (MCD) and IgA nephropathy (IgAN), claimed to be found in an overwhelming number in some Asian regions. We retrospectively analyzed clinical and histological data from 627 renal biopsies, performed in our department from January 2002 to January 2005 and completed electron microscopy in 112 specimens diagnosed as IgAN. The coincidence of IgAN and MCD was found in 8 patients (7.1%). The coincidence of IgAN and minimal change nephrotic syndrome (MCNS) clinically--especially presence of nephrotic syndrome and the response to drug therapy (with corticosteroids)--behaves as "pure" MCN. Our data from Czech Republic seem to suggest that the combination of IgAN with MCNS can be found relatively frequently not only in Asian patients (as stressed by some authors of Asian origin) but also in European inhabitants. The pathogenesis of the coincidence of IgAN and MCD needs to be elucidated by further studies.
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