Hostname: page-component-cd9895bd7-jn8rn Total loading time: 0 Render date: 2024-12-24T03:13:52.098Z Has data issue: false hasContentIssue false

P.046 Extensive leukoencephalopathy as a differential diagnosis of motor neuron disease: case report and literature review

Published online by Cambridge University Press:  24 June 2022

JC Becerra-Mateus
Affiliation:
(Medellín)*
MJ Hidalgo-Ramírez
Affiliation:
(Medellín)
DF Aguillón-Niño
Affiliation:
(Medellín)
J Gómez-Ramírez
Affiliation:
(Medellín)
CA Villegas-Lanau
Affiliation:
(Medellín)
Rights & Permissions [Opens in a new window]

Abstract

Core share and HTML view are not available for this content. However, as you have access to this content, a full PDF is available via the ‘Save PDF’ action button.

Background: Weakness is frequently a reason to attend neurology consultation which entails a challenge due to its wide range of diagnostic possibilities. We present the case of an elderly woman with long-standing right upper limb weakness. Methods: Patient data was obtained from medical records and an extensive neuropathological evaluation was performed. Results: Weakness started off in her right hand, which progressed insidiously to her right hemibody. with hyperreflexia, atrophy, fasciculations and foot drop. Subsequently, bulbar and left hemibody deterioration began. She died due to ventilatory failure four years after the first symptom appeared. A tigroid pattern in the neuroimaging studies suggest white matter involvement, while the neuropathological studies showed loss of motor neurons in the spinal cord. Conclusions: The available evidence does not allow us to dismiss the hypothesis of a motor neuron disease or a leukodystrophy. Cases like this one establish a diagnostic challenge due to their complexity and unusual etiology.

Type
Poster Presentations
Copyright
© The Author(s), 2022. Published by Cambridge University Press on behalf of Canadian Neurological Sciences Federation