Spontaneous resolution of acquired factor X deficiency in amyloidosis

J Intern Med. 1993 Sep;234(3):329-30. doi: 10.1111/j.1365-2796.1993.tb00751.x.

Abstract

We describe the case of a 51-year-old man with systemic amyloidosis in whom factor X activity was initially 6% of the normal. Amyloidosis was responsible for congestive heart failure and a nephrotic syndrome but there was no bleeding diathesis. A 12-month trial of melphalan and prednisone failed to improve cardiac and renal dysfunction; factor X levels remained low. Eighteen months after this treatment was stopped, factor X spontaneously normalized although renal insufficiency persisted. We suggest that the possibility of a spontaneous factor X recovery must be considered when evaluating efficacy of therapeutic agents in amyloidosis.

Publication types

  • Case Reports

MeSH terms

  • Amyloidosis / complications*
  • Factor X Deficiency / blood*
  • Factor X Deficiency / complications
  • Humans
  • Male
  • Middle Aged
  • Remission, Spontaneous