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Intramedullary cervical spinal cord sarcoidosis
1Department of Neurology, SUNY Downstate Medical Center, Brooklyn, NY 11203, USA. sbhagavati@downstate.edu
Spinal Cord
|June 11, 2008
Summary
This case report highlights an uncommon presentation of cervical spinal cord sarcoidosis. Early steroid treatment led to complete recovery, avoiding surgery for a suspected tumor.
Area of Science:
- Neurology
- Immunology
- Oncology
Background:
- Sarcoidosis is a multisystem inflammatory disease of unknown etiology.
- Intramedullary spinal cord sarcoidosis is rare, often presenting with non-specific neurological deficits.
- Differential diagnosis includes primary and secondary spinal cord tumors.
Observation:
- A 47-year-old male presented with progressive leg heaviness, gait difficulty, and sensory disturbances.
- MRI revealed a contrast-enhancing intramedullary lesion mimicking a spinal tumor.
- Systemic investigations uncovered mediastinal lymphadenopathy and elevated angiotensin-converting enzyme (ACE) levels.
Findings:
- Transbronchial lung biopsy confirmed sarcoidosis.
- The patient received prompt corticosteroid therapy.
- Complete clinical and radiological resolution of the spinal cord lesion was achieved within 4 weeks and maintained over 18 months.
Implications:
- Intramedullary spinal cord lesions with tumor-like enhancement warrant investigation for sarcoidosis.
- Considering sarcoidosis in the differential diagnosis can prevent unnecessary neurosurgical intervention.
- Steroid therapy is an effective treatment for spinal cord sarcoidosis, leading to favorable outcomes.
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