Membranoproliferative glomerulonephritis

ISSN: 00471852
0Citations
Citations of this article
15Readers
Mendeley users who have this article in their library.

Abstract

MPGN is characterized by its peculiar histological findings; lobular appearance, cellular and mesangial matrix proliferation and double contoured capillary loops. Based on histomorphalogical pattern, three types are subdivided. MPGN may be primary (in most children) or secondary (in most adults) to chronic infections, cryoglobulinemia or systemic autoimmune disorders. Clinical manifestation of typical MPGN is nephrotic range proteinuria associated with microscopic hematuria, showing slowly progressive course. Treatment strategy is composed of exclusion of pathogen, especially in HCV positive MPGN, and intervention to autoimmune mechanism such as alternative-day steroid regimen.

Cite

CITATION STYLE

APA

Taguma, Y., Chiba, S., & Sato, H. (2004). Membranoproliferative glomerulonephritis. Nippon Rinsho. Japanese Journal of Clinical Medicine.

Register to see more suggestions

Mendeley helps you to discover research relevant for your work.

Already have an account?

Save time finding and organizing research with Mendeley

Sign up for free