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Characterizing Lewis Pairs Using Titration Coupled with In Situ Infrared Spectroscopy
Published on: February 20, 2020
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[About a Case of Lewis-Sumner Syndrome Observed in Niger]
H Assadeck1,2, M Toudou Daouda1, F Hassane Djibo1
1Service de neurologie, Hôpital national de Niamey, Niger.
Bulletin De La Societe De Pathologie Exotique (1990)
|April 6, 2019
Summary
This case study documents Lewis-Sumner syndrome in Niger, a rare neurological disorder. Prompt treatment with intravenous immunoglobulins led to a good clinical response in the patient.
Area of Science:
- Neurology
- Clinical Neuroscience
- Rare Diseases
Background:
- Lewis-Sumner syndrome (LSS) is a rare, immune-mediated peripheral neuropathy.
- It is characterized by asymmetric, predominantly upper limb, sensory and motor deficits.
- Diagnosis often relies on clinical presentation and electrophysiological findings.
Observation:
- A 53-year-old man in Niger presented with paresthesia following a flu-like illness.
- Symptoms rapidly progressed to asymmetric sensitivomotor involvement of all four limbs, favoring upper limbs.
- Electrophysiology showed motor conduction blocks and reduced sensory amplitudes/velocities.
Findings:
- Cerebrospinal fluid analysis revealed elevated protein without signs of meningitis.
- Other systemic and infectious causes were excluded.
- Clinical and electrophysiological data confirmed the diagnosis of Lewis-Sumner syndrome.
Implications:
- This report highlights the first documented case of Lewis-Sumner syndrome in Niger.
- Intravenous immunoglobulin therapy demonstrated a positive clinical outcome.
- Increased awareness of LSS in diverse geographical settings is crucial for timely diagnosis and management.
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