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[Pure spinal cysticercosis. Note on the cerebrospinal fluid]
Revue Neurologique
|January 1, 1984
Summary
Neurocysticercosis caused extensive spinal cord cysts in a Benin patient, leading to severe neurological deficits. The condition proved resistant to Praziquantel treatment, highlighting diagnostic and therapeutic challenges.
Area of Science:
- Neurology
- Infectious Diseases
- Parasitology
Background:
- Cysticercosis, a parasitic infection caused by the larval cysts of the tapeworm Taenia solium, can affect various organs, including the central nervous system.
- Spinal cysticercosis is a rare manifestation, often presenting with symptoms mimicking other spinal cord pathologies.
Observation:
- A patient from Benin presented with progressive bilateral sciatic pain and sensorimotor deficits in the lower limbs.
- Symptoms evolved to include thoracic spinal cord compression, with myelography revealing numerous intrathecal cysts from the cauda equina to the cervical cord.
- Cerebrospinal fluid (CSF) analysis demonstrated eosinophils, elevated protein levels, and local synthesis of immunoglobulin G with an oligoclonal profile.
Findings:
- Diagnosis of cysticercosis was confirmed by examining cysts obtained during lumbar laminectomy.
- Accidental cyst puncture showed cerebrospinal fluid with protein migration and local immunoglobulin A synthesis.
- Treatment with Praziquantel was ineffective in resolving the parasitic cysts or improving neurological symptoms.
Implications:
- This case underscores the potential for extensive spinal involvement in neurocysticercosis, presenting diagnostic challenges due to its rarity and varied presentation.
- The findings highlight the importance of considering cysticercosis in endemic regions, even with atypical neurological symptoms.
- The ineffectiveness of Praziquantel suggests potential limitations in current treatment protocols for severe or disseminated spinal cysticercosis, warranting further research into alternative therapeutic strategies.