We present a patient with AL amyloidosis who had an autologous stem cell transplant (ASCT) over 9 years ago. She has since then developed slowly progressive renal insufficiency and the nephrotic syndrome. Hematologic evaluation has failed to identify recurrent disease and a renal biopsy demonstrated extensive amyloid deposition and substantial glomerulosclerosis. We suggest that the patient has chronic glomerulosclerosis as a consequence of renal damage associated with her disease process and her treatment. Copyright © Informa Healthcare USA, Inc.
CITATION STYLE
Rifkin, S. I., & Weinstein, S. S. (2012). Late onset renal failure and nephrotic syndrome after autologous stem cell transplant for AL amyloidosis. Renal Failure, 34(5), 664–666. https://doi.org/10.3109/0886022X.2012.669320
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