Amyloidosis is a syndrome characterized by deposition of a highly insoluble protein material in the extracellular space that may affect several organs. It may be generalized and idiopathic (primary amyloidosis). We describe the case of a 48 years-old woman with axonal neuropathy associated with proteinuria, whose final investigation resulted in diagnosis of primary amyloidosis (AL). She was submitted to autologous bone marrow transplantation. We discuss some aspects related to diagnosis of neuropathy and current treatment of AL.
CITATION STYLE
Povoas Barsottini, O. G., Arantes, A., Sigulem, D., Kutner, J. M., Feitosa Ribeiro, A. A., Moura, L. A., & Hamerschlak, N. (2004). Axonal neuropathy as initial manifestation of primary amyloidosis: Report of a case submitted to bone marrow transplantation. Arquivos de Neuro-Psiquiatria, 62(3 A), 725–729. https://doi.org/10.1590/s0004-282x2004000400030
Mendeley helps you to discover research relevant for your work.