| Literature DB >> 14750118 |
Sapna Shah1, Jamie Cavenagh, Michael Sheaf, Raj C Thuraisingham.
Abstract
Collapsing focal segmental glomerulosclerosis can be idiopathic but has been associated with human immunodeficiency virus infection as well as lymphoproliferative, myeloproliferative, and autoimmune disorders. It has a more rapid progression to end-stage renal failure. Treatment of this condition is poorly defined with no clear evidence of response to any treatment regimens. We report a case of collapsing focal segmental glomerulosclerosis in association with multiple myeloma that underwent partial remission following treatment for the underlying disease.Entities:
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Year: 2004 PMID: 14750118 DOI: 10.1053/j.ajkd.2003.10.036
Source DB: PubMed Journal: Am J Kidney Dis ISSN: 0272-6386 Impact factor: 8.860