Ann Clin Neurophysiol.  2018 Jul;20(2):101-104. 10.14253/acn.2018.20.2.101.

Electrophysiological and radiological evidence for the multifocal nature of a case of multifocal acquired demyelinating sensory and motor neuropathy

Affiliations
  • 1Department of Neurology, Hallym University Sacred Heart Hospital, Anyang, Korea.
  • 2Department of Neurology, Kangdong Sacred Heart Hospital, Seoul, Korea.
  • 3Department of Neurology, Haedong Hospital, Busan, Korea. sanghyoryu@gmail.com

Abstract

Multifocal acquired demyelinating sensory and motor (MADSAM) neuropathy is a variant of chronic acquired demyelinating polyneuropathy. A 65-year-old women presented with upper arm weakness. A nerve conduction study showed conduction blocks over intermediate segments with sparing of distal compound action potentials. Magnetic resonance imaging revealed asymmetric hypertrophy of the brachial plexus on the affected side. These findings represent important electrophysiological and radiological evidence of MADSAM neuropathy. The condition of the patient began to improve after starting intravenous immunoglobulin administration.

Keyword

Polyneuropathy, Chronic inflammatory demyelinating; Neural conduction; Magnetic resonance imaging

MeSH Terms

Action Potentials
Aged
Arm
Brachial Plexus
Female
Humans
Hypertrophy
Immunoglobulins
Magnetic Resonance Imaging
Neural Conduction
Polyneuropathies
Immunoglobulins

Figure

  • Fig. 1. Findings of the motor nerve conduction study of the right ulnar nerve. The distal motor latency and the compound muscle action potentials were normal at the wrist and below the elbow. Conduction block was observed between above and below the elbow. NCV, nerve conduction velocity.

  • Fig. 2. Brachial plexus magnetic resonance imaging (Short T1 Inversion Recovery Image, non-contrast enhanced) revealed fusiform hypertrophy of the right C5-C8 roots, and plexus was observed (arrows). No hypertrophy was observed on the left side.


Reference

References

1. Kuwabara S, Misawa S. Chronic inflammatory demyelinating polyneuropathy: clinical subtypes and their correlation with electrophysiology. Clin Exp Neuroimmunol. 2011; 2:41–48.
Article
2. Shibuya K, Sugiyama A, Ito S, Misawa S, Sekiguchi Y, Mitsuma S, et el. Reconstruction magnetic resonance neurography in chronic inflammatory demyelinating polyneuropathy. Ann Neurol. 2015; 77:333–337.
3. Ad Hoc Subcommittee of the American Academy of Neurology AIDS Task Force. Research criteria for the diagnosis of chronic inflammatory demyelinating polyneuropathy (CIDP). Neurology. 1991; 41:617–618.
4. Van den Bergh PY, Hadden RD, Bouche P, Cornblath DR, Hahn A, Illa I, et el. European Federation of Neurological Societies/Peripheral Nerve Society guideline on management of chronic inflammatory demyelinating polyradiculoneuropathy: report of a joint task force of the European Federation of Neurological Societies and the Peripheral Nerve Society – first revision. Eur J Neurol. 2010; 17:356–363.
5. Viala K, ReniéL, Maisonobe T, Béhin A, Neil J, Léger JM, et el. Follow-up study and response to treatment in 23 patients with Lewis-Sumner syndrome. Brain. 2004; 127(Pt 9):2010–2017.
6. Park YE, Yook JW, Kim DS. A case of Lewis-Sumner syndrome showing dramatic improvement after plasma exchange. J Korean Med Sci. 2010; 25:1101–1104.
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