A rare adult case with diffuse segmental membranous glomerulonephritis

6Citations
Citations of this article
7Readers
Mendeley users who have this article in their library.

Abstract

A 71-year-old man with hypertension and diabetes mellitus presented with proteinuria. Laboratory data showed proteinuria of 3.1 g/g creatinine, serum albumin of 3.5 g/dL and serum creatinine of 1.03 mg/dL without autoantibodies. A renal biopsy revealed segmental granular IgG depositions on glomerular capillary walls. Electron microscopy showed segmentally subepithelial, intramembranous and mesangial deposits. Diffuse segmental membranous glomerulonephritis (MGN) was diagnosed with only IgG1 deposition and without M-type phospholipase A2 receptor or thrombospondin type-1 domain-containing 7A staining, suggesting secondary MGN with an unknown target antigen in immune deposits. Physicians should keep in mind the existence of segmental MGN to better understand the clinicopathological characteristics.

Cite

CITATION STYLE

APA

Fujigaki, Y., Tamura, Y., Shibata, S., Kondo, F., Iwakura, T., Kojima, K., … Uchida, S. (2017). A rare adult case with diffuse segmental membranous glomerulonephritis. Internal Medicine, 56(13), 1691–1695. https://doi.org/10.2169/internalmedicine.56.8298

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