Axoval neuropathy as initial manifestation of primary amyloidosis: report of a case submitted to bone marrow transplantation

Arq Neuropsiquiatr. 2004 Sep;62(3A):725-9. doi: 10.1590/s0004-282x2004000400030. Epub 2004 Aug 24.

Abstract

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.

Publication types

  • Case Reports

MeSH terms

  • Amyloid Neuropathies / etiology*
  • Amyloid Neuropathies / pathology
  • Amyloid Neuropathies / therapy
  • Amyloidosis / complications*
  • Amyloidosis / pathology
  • Amyloidosis / therapy
  • Bone Marrow Transplantation*
  • Female
  • Hematopoietic Stem Cell Transplantation
  • Humans
  • Middle Aged