[Progressive muscular atrophy: clinical and laboratory study in eleven patients]

Arq Neuropsiquiatr. 2004 Mar;62(1):119-26. doi: 10.1590/s0004-282x2004000100021. Epub 2004 Apr 28.
[Article in Portuguese]

Abstract

Progressive muscular atrophy (PMA), an infrequent type of motor neuron disease (MND), is a predominantly lower motor neuron degeneration, causing muscle wasting and weakness with loss of weight and fasciculations. The diagnosis is based on rigid criteria, considering clinical aspects and eletroneuromyography findings. Blood tests and radiological investigation are necessary to look for other diagnosis mimicking PMA. We herein present 11 patients with PMA (5.9% of all our MND patients), 9 men and 2 women, which onset of symptoms occurred mainly under de age of 50, with a mean of 45.5 years. Cramp was the most frequent symptom preceding muscular weakness. Muscle pain, fatigue and fasciculations were also cited as starting symptoms. Asymmetric weakness of the arms was the most frequent pattern of onset of the disease. Bulbar muscular weakness developed in all patients during the course of the disease. Predisposing factors and distinctive clinical outcome was not observed in any of the patients. Ophthalmoparesis and sphincter dysfunction were seen in two patients who had a prolonged time in artificial respiratory assistance. Immunosuppressive therapy was ineffective in all patients. Progressive course was seen in all cases and the mean survival time was 44 months.

Publication types

  • English Abstract

MeSH terms

  • Adjuvants, Immunologic / therapeutic use
  • Adult
  • Aged
  • Female
  • Humans
  • Immunosuppressive Agents / therapeutic use
  • Male
  • Middle Aged
  • Muscular Atrophy, Spinal / diagnosis*
  • Muscular Atrophy, Spinal / drug therapy
  • Muscular Atrophy, Spinal / mortality
  • Survival Analysis

Substances

  • Adjuvants, Immunologic
  • Immunosuppressive Agents