Sporadic lower motor neuron disease with Lewy body-like inclusions: a new subgroup?

T. Kato, T. Katagiri, A. Hirano, H. Sasaki, S. Arai

Research output: Contribution to journalArticle

36 Scopus citations

Abstract

A sporadic case of lower motor neuron disease with Lewy body-like inclusions is presented. A woman of 69, 6 months before death, had a history of muscle weakness and atrophy of the four extremities. Neuropathological examination revealed neuronal loss and associated gliosis in the anterior horns of the whole spinal cord. The cytoplasm of some of the remaining neurons contained Lewy body-like inclusions, Bunina bodies, or both. Spheroids and cordlike thickenings of cell processes were also observed in the anterior horns. A few neurons showed argentophilia of the cytoplasm. No tract degeneration was detectable in the white matter of the spinal cord. The present case and two reported similar cases may constitute a new subgroup of motor neuron disease.

Original languageEnglish (US)
Pages (from-to)208-211
Number of pages4
JournalActa neuropathologica
Volume76
Issue number2
DOIs
StatePublished - Mar 1 1988

Keywords

  • Bunina bodies
  • Cord-like thickenings of cell processes
  • Familial amyotrophic lateral sclerosis
  • Lewy body-like inclusions
  • Sporadic lower motor neuron disease

ASJC Scopus subject areas

  • Pathology and Forensic Medicine
  • Clinical Neurology
  • Cellular and Molecular Neuroscience

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