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Intern Med ; 55(18): 2707-12, 2016.
Article in English | MEDLINE | ID: mdl-27629972

ABSTRACT

A 70-year-old woman with Charcot-Marie-Tooth disease (CMT) suffered from nephrotic syndrome and a renal biopsy revealed non-AA amyloid depositions that contained immunoglobulin light chain λ. Her serum λ free LC was elevated to 80.8 mg/L and she was diagnosed with primary amyloid light-chain (AL) amyloidosis. She was subsequently treated with lenalidomide, cyclophosphamide, and dexamethasone (RCD). After 14 cycles of RCD, she achieved complete remission. Her serum albumin levels gradually normalized to 3.1 g/dL. No exacerbation of neurologic symptoms related to CMT was observed. Thus, RCD may be a well-tolerated and effective regimen for treating AL amyloidosis in patients with CMT disease.


Subject(s)
Amyloidosis/drug therapy , Amyloidosis/etiology , Charcot-Marie-Tooth Disease/complications , Immunosuppressive Agents/therapeutic use , Aged , Cyclophosphamide/therapeutic use , Dexamethasone/therapeutic use , Drug Therapy, Combination , Female , Humans , Immunoglobulin Light Chains/immunology , Immunoglobulin Light-chain Amyloidosis , Immunoglobulin lambda-Chains/immunology , Immunosuppressive Agents/administration & dosage , Lenalidomide , Remission Induction , Thalidomide/analogs & derivatives , Thalidomide/therapeutic use
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