Abstract
Three adolescents with unilateral renal vein thrombosis and the nephrotic syndrome are presented. Light, fluorescent, and electron microscopic examination of bilateral renal biopsy specimens in each patient demonstrated membranous glomerulonephritis in both kidneys. In the first case there was no evidence of preexisting renal disease and the initial biopsy at the time of thrombosis revealed near normal glomeruli on light microscopy. Fluorescent staining and the electron microscope demonstrated immune complex deposition along the glomerular basement membrane. Follow-up biopsy of the same case seven months later showed advanced membranous glomerubonephritis on light and electron microscopy. These cases as well as data from recent animal experiments raise the interesting suggestion that renal vein thrombosis and the nephrotic syndrome might be an immunologic disease. Unilateral obstruction of the renal vein may result in renal antigen release and antigen-antibody complex formation with subsequent glomerular deposition, bilateral glomerular disease, and the nephrotic syndrome.
- Received June 18, 1971.
- Accepted May 4, 1972.
- Copyright © 1972 by the American Academy of Pediatrics
Individual Login
Institutional Login
You may be able to gain access using your login credentials for your institution. Contact your librarian or administrator if you do not have a username and password.
Log in through your institution
Pay Per Article - You may access this article (from the computer you are currently using) for 2 days for US$25.00
Regain Access - You can regain access to a recent Pay per Article purchase if your access period has not yet expired.