AL amyloidosis is an infiltrative disorder characterized by the extrac
ellular deposition of insoluble fibrillar immunoglobulin light chains
whose production results from a plasma cell dyscrasia. Treatment with
melphalan has resulted in an improvement in a few patients. Recently,
intensive chemotherapy followed by autologous or syngeneic stem cell s
upport has been shown to offer potential benefit. Allogeneic stem cell
support after intensive therapy would retain the benefits of autologo
us transplantation, with the additional advantages of a tumor-free gra
ft and of a possible graft-versus-tumor effect. We report a patient wi
th AL amyloidosis and significant proteinuria, She improved after an a
llogeneic bone marrow transplantation.