Chronic kidney disease after autologous stem cell transplantation: analysis of a single center experience.

Int Urol Nephrol

Department of Nephrology, The First Affiliated Hospital, Guangxi Medical University, No. 22, Shuang Yong Lu, Nanning, 530021, Guangxi, China.

Published: July 2014

AI Article Synopsis

  • This study looked at how often chronic kidney disease (CKD) happens in patients who received a specific type of stem cell transplant called autologous HSCT.
  • Out of 41 patients, 6 developed CKD, and many had symptoms like protein in their urine or nephrotic syndrome (a type of kidney problem).
  • The study found that a certain kidney problem called mesangial proliferative glomerulonephritis was present in some patients, and taking a medicine called prednisone helped many of them.

Article Abstract

Purpose: Chronic kidney disease (CKD) after allogeneic hematopoietic stem cell transplantation (HSCT) has increasingly been reported. However, CKD after autologous HSCT, especially changes in renal pathology, has rarely been reported. This study aimed to evaluate the frequency of CKD among patients who received autologous HSCT for hematological and nonhematological disorders, and analyze its clinical and pathological features.

Methods: We performed a retrospective study to evaluate the frequency of CKD after autologous HSCT and analyzed clinical and pathological features of CKD. Clinical records of patients who underwent autologous HSCT at the First Affiliated Hospital of Guangxi Medical University between May 2000 and November 2010 were screened. Clinical data of those with kidney injury on presentation and follow-up were acquired from hospital records.

Results: A total of 41 patients who received autologous HSCT were identified. CKD developed in six patients (14.6%). Among the six patients, all had various degrees of proteinuria and three patients had nephrotic syndrome. Impaired renal function occurred in three patients. Three patients with nephrotic syndrome received only prednisone. Two patients obtained complete remission, and one had partial remission. What is particularly worth mentioning is, in two patients who received renal biopsy in our study, the pathological changes were mesangial proliferative glomerulonephritis.

Conclusions: Mesangial proliferative glomerulonephritis may not be as uncommon as previously thought in CKD patients after autologous HSCT. Presentation of nephrotic syndrome is common in CKD after HSCT and prednisone alone are effective.

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http://dx.doi.org/10.1007/s11255-014-0683-4DOI Listing

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