Rapidly Progressive Glomerulonephritis (RPGN): Is there Still an “Idiopathic” Subgroup? View Full Text


Ontology type: schema:Chapter     


Chapter Info

DATE

1993

AUTHORS

F. Ferrario , M. Tadros , P. Napodano , A. Giordano , R. A. Sinico , G. Fellin , G. D’Amico

ABSTRACT

In order to clarify if “idiopathic” RPGN still exists as a distinct entity we reviewed 41 patients with histological picture of diffuse crescentic GN (60% of crescents) and no clinical evidence of systemic disease. According to the presence or absence of intraglomerular necrotizing lesions we subdivided the patients into two different morphological groups: Group I (25 pts) with necrotizing GN and massive periglomerular infiltrates; Group II (16 pts) with intra-extracapillary proliferation and no interstitial infiltrates. Our data suggest that “idiopathic” RPGN does not exist as a distinct entity, but is an expression either of renal limited vasculitis or crescentic GN complicating primary proliferative GN. More... »

PAGES

431-434

Identifiers

URI

http://scigraph.springernature.com/pub.10.1007/978-1-4757-9182-2_76

DOI

http://dx.doi.org/10.1007/978-1-4757-9182-2_76

DIMENSIONS

https://app.dimensions.ai/details/publication/pub.1030285023

PUBMED

https://www.ncbi.nlm.nih.gov/pubmed/8296650


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