Division of Nephrology and Hypertension, University of South Florida College of Medicine, Tampa, FL, USA.
Ren Fail. 2012;34(5):664-6. doi: 10.3109/0886022X.2012.669320. Epub 2012 Mar 27.
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.
我们报告了一位患有 AL 淀粉样变性的患者,她在 9 年前接受了自体干细胞移植(ASCT)。此后,她逐渐出现肾功能不全和肾病综合征。血液学评估未能发现复发疾病,肾活检显示广泛的淀粉样物质沉积和大量肾小球硬化。我们认为,患者患有慢性肾小球硬化症,这是由于她的疾病过程和治疗引起的肾脏损伤所致。