Collagenofibrotic glomerulopathy – rare glomerulonephritis
Authors:
G. Bernasovská 1; M. Demeš 1; A. Okša 1,2; M. Pavlovič 1; A. Vahančík 1; O. Nyitrayová 3; P. Gomolčák 3; D. Daniš 3
Authors‘ workplace:
I. interná klinika Slovenskej zdravotníckej univerzity a FNsP Bratislava, pracovisko Kramáre, Slovenská republika, prednosta prim. prof. MUDr. Štefan Hrušovský, CSc., Dr. SVS
1; Oddelenie klinickej a experimentálnej farmakoterapie Slovenskej zdravotníckej univerzity Bratislava, Slovenská republika, vedúci h. doc. MUDr. Martin Gajdoš, CSc.
2; Ústav patológie FNsP Bratislava, pracovisko Kramáre, Slovenská republika, vedúci doc. MUDr. Dušan Daniš, CSc
3
Published in:
Vnitř Lék 2006; 52(12): 1200-1204
Category:
Case Report
Práca bola prednesená 19. 9. 2004 na sympóziu s medzinárodnou účasťou Kvalita starostlivosti o nefrologického, dialyzovaného a transplantovaného pacienta, Zemplínska Šírava, Slovenská republika.
Overview
Glomerulopathies with fibrillary deposits form a heterogeneous group of renal diseases that can be identified only by means of electron microscopy. A case of rare type of such a nephropathy, the collagenofibrotic glomerulopathy with focus on differential diagnostics is presented and a review of current knowledge on this renal disease is given.
Key words:
fibrillary glomerulopathies - collagenofibrotic glomerulopathy - electron microscopy
Sources
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Labels
Diabetology Endocrinology Internal medicineArticle was published in
Internal Medicine
2006 Issue 12
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