Literature DB >> 15786823

Resolution of primary amyloidosis by melphalan and prednisolone: a case report.

M Nakayama1, M Kashiwagi, R Katafuchi, K Hori, S Hayashi, S Fujimi.   

Abstract

We here report a case of a 50-year-old man who showed histologically evident resolution of primary amyloidosis by melphalan and prednisolone. The patient was admitted to our hospital for further evaluation of nephrotic syndrome and remarkable hepatomegaly with refractory ascites, on September 11, 1998. Laboratory tests at presentation showed nephrotic syndrome with slight renal impairment and elevation of the enzymes of the biliary system. Monoclonal light chains were not detected in the serum or urine by immunoelectrophoresis. A renal biopsy revealed global deposition of amyloid in all glomeruli, interstitium and blood vessels. Immunofluorescence staining was positive for kappa light chains. Liver biopsy specimens showed extensive deposition of amyloid along sinusoid walls. Bone marrow aspiration contained 7% plasma cells but no clusters or abnormal cells. Based on these findings, systemic AL- (amyloid light chain) amyloidosis was diagnosed, and the treatment with combinations of melphalan and prednisolone was started from October 1998 at intervals of 4-6 weeks. Renal impairment progressed, resulting in the initiation of maintenance hemodialysis in February 1999. Reinfusion of ascitic fluid into the hemodialysis circuit had been performed from March 1999 for refractory ascites, and ascites disappeared in July 1999. Furthermore, urinary output increased after 14 courses of chemotherapy. Renal function gradually ameliorated with a concomitant reduction in the enzymes of biliary system, and finally hemodialysis was discontinued in April 2001. Sixteen courses of chemotherapy were administered by April 2001. Proteinuria was negative in August 2001. A second renal biopsy was performed on November 20, 2001, which showed markedly decreased amyloid deposition and a proliferation of mesangial cells and increase in matrix in various degrees. We report a case of a patient with primary amyloidosis who was successfully treated by melphalan and prednisolone, resulting in marked resolution of renal amyloidosis.

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Year:  2005        PMID: 15786823     DOI: 10.5414/cnp63215

Source DB:  PubMed          Journal:  Clin Nephrol        ISSN: 0301-0430            Impact factor:   0.975


  3 in total

1.  Secondary amyloidosis in Crohn's disease: treatment with tumour necrosis factor inhibitor.

Authors:  M M Boscá; C M Pérez-Baylach; M A Solis; R Antón; E Mayordomo; S Pons; M Mínguez; A Benages
Journal:  Gut       Date:  2006-02       Impact factor: 23.059

2.  Regression of renal amyloid deposits by VAD therapy plus autologous stem cell transplantation in a patient with primary AL amyloidosis.

Authors:  Naoya Toriu; Naoki Sawa; Rikako Hiramatsu; Hiroki Mizuno; Daisuke Ikuma; Akinari Sekine; Noriko Hayami; Keiichi Sumida; Masayuki Yamanouchi; Eiko Hasegawa; Junichi Hoshino; Kenmei Takaichi; Atsushi Wake; Kenichi Ohashi; Takeshi Fujii; Yoshifumi Ubara
Journal:  CEN Case Rep       Date:  2019-09-14

Review 3.  Value of repeat renal biopsy in the evaluation of AL amyloidosis patients lacking renal response despite of complete hematologic remission: a case report and literature review.

Authors:  Ping Zhang; Xiuling Chen; Yurong Zou; Wei Wang; Yunlin Feng
Journal:  BMC Nephrol       Date:  2022-03-31       Impact factor: 2.388

  3 in total

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