Two cases of Type Ⅲ collagen glomerulopathy and literature review / 中南大学学报(医学版)
Journal of Central South University(Medical Sciences)
; (12): 869-873, 2020.
Article
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| ID: wpr-827400
Responsable en Bibliothèque :
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ABSTRACT
In this paper, 2 cases of collagen Type Ⅲ glomerulopathy were analyzed. The clinical manifestations mainly included nephrotic syndrome, proteinuria, hypertension and renal dysfunction. One patient showed that the complement factor H-related protein 5 (CFHR5) gene was likely a disease-causing mutation. The pathological examination of renal tissues showed hyperplasia of mesangial matrix, sub-endothelial insertion, and double-track formation. Immunohistochemistry of Type III collagen was positive. Electron microscopy revealed that massive collagen fibers (40-70 nm in diameter) deposited in the mesangial matrix and basement membrane. As for the follow-up results, the normal renal function had kept steady and the proteinuria was moderate in 1 case treated with angiotensin Ⅱ receptor blocker. Due to other system disease, another case developed into acute kidney injury and then received hemodialysis. The clinical manifestations of collagen Type Ⅲ glomerulopathy was atypical, the light microscope pathological features were various, and the disease was mainly diagnosed by electron microscopy and immunohistochemistry.
Texte intégral:
1
Indice:
WPRIM
Sujet Principal:
Protéinurie
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Collagène de type III
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Génétique
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Mésangium glomérulaire
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Maladies du rein
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Glomérule rénal
Limites du sujet:
Humans
langue:
En
Texte intégral:
Journal of Central South University(Medical Sciences)
Année:
2020
Type:
Article