Acta Clinica Croatica (Jan 2018)

Multifocal Motor Neuropathy: Case Reports

  • Edin Jusufović,
  • Osman Sinanović,
  • Sanela Zukić,
  • Adnan Burina,
  • Zlatka Džinić Jusufović,
  • Alma Šakić

DOI
https://doi.org/10.20471/acc.2018.57.03.23
Journal volume & issue
Vol. 57., no. 3.
pp. 581 – 587

Abstract

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Multifocal motor neuropathy (MMN) is a chronic demyelinating neuropathy mainly characterized by multifocal distribution; affecting only motor nerve fibers of two or more peripheral nerves, with the absence of symptoms and signs of upper motor neuron; chronic, sometimes cascading progressive course; demyelination with partial block of motor conduction; immune-mediated pathogenesis and good response to intravenous immunoglobulin treatment (IVIG). The diagnosis of MMN is based on clinical, laboratory and electrophysiological characteristics. Steroids are ineffective in MMN and may lead to worsening of the disease. Similarly, therapeutic plasma exchange is negligibly effective in this neuropathy. However, more than 80% of patients with MMN experience improvement after IVIG. We present our three cases of MMN with positive response to IVIG.

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