| Literature DB >> 20473542 |
Kunihiro Maeda1, Keisuke Suzuki, Motonori Mizutani, Hitoshi Watanabe, Norihiro Suga, Wataru Kitagawa, Naoto Miura, Kazuhiro Nishikawa, Kazuharu Uchida, Hirokazu Imai.
Abstract
A 23-year-old Japanese man who had undergone hematopoietic stem cell transplantation for acute lymphocytic leukemia from an HLA-identical sibling 6 years earlier developed proteinuria and impaired kidney function. Kidney biopsy revealed thrombotic microangiopathy with a moderate increase in mesangial matrices and glomerular microaneurysm featuring retention of red blood cells. The patient's kidney function gradually deteriorated, requiring the institution of treatment with angiotensin II receptor blockers and angiotensin-converting enzyme inhibitors, and progressing to continuous ambulatory peritoneal dialysis 4 years after the initial kidney biopsy. Eventually, kidney transplantation was performed with his mother as the donor. His kidney function is stable on immunosuppressive drugs at 2 years after transplantation. This report reflects the growing number of patients with chronic kidney disease with thrombotic microangiopathy all over the world.Entities:
Mesh:
Year: 2010 PMID: 20473542 DOI: 10.1007/s10157-010-0292-1
Source DB: PubMed Journal: Clin Exp Nephrol ISSN: 1342-1751 Impact factor: 2.801