# Acute Spinal Cord Syndrome As the Initial Manifestation of Multiple Sclerosis: A Case Report

**Authors:** Catarina Pinto Silva, Cristiana Fernandes, Márcia Ribeiro, Dany Cruz

PMC · DOI: 10.7759/cureus.98644 · Cureus · 2025-12-07

## TL;DR

A young man with no prior health issues developed acute spinal cord symptoms, which turned out to be the first sign of multiple sclerosis.

## Contribution

This case highlights the rare but important presentation of MS as an isolated spinal cord syndrome.

## Key findings

- MRI showed two spinal cord lesions and a brain lesion consistent with demyelination.
- CSF analysis revealed lymphocytic pleocytosis and oligoclonal bands, supporting an MS diagnosis.
- Treatment with high-dose steroids led to significant neurological improvement.

## Abstract

Multiple sclerosis (MS) typically presents with optic neuritis, brainstem syndromes, or sensory disturbances. Isolated spinal cord involvement as the initial manifestation occurs in fewer than 30% of cases, making early recognition challenging but essential for timely diagnosis and treatment initiation.

A previously healthy 22-year-old Caucasian male presented with an acute onset of mid-thoracic pain followed by progressive sensory deficits below the T10 dermatome and lower limb weakness developing over five days. Neurological examination revealed spastic paraparesis (Medical Research Council grade 3/5), sensory level at T10, and hyperreflexia with bilateral Babinski signs. Magnetic resonance imaging (MRI) of the spinal cord demonstrated two focal T2-hyperintense intramedullary lesions at T1-T2 and T11 levels with gadolinium enhancement. Brain MRI revealed a single periventricular lesion consistent with demyelination. Cerebrospinal fluid analysis showed lymphocytic pleocytosis (11 cells/µL), mildly elevated protein (52 mg/dL), and two oligoclonal bands restricted to cerebrospinal fluid (CSF). The patient received high-dose intravenous methylprednisolone (1 g daily for three days) with significant neurological improvement. At the three-month follow-up, motor strength had improved to grade 4/5 with residual mild sensory deficits.

This case illustrates the diagnostic challenges of MS presenting as isolated spinal cord syndrome. Early spinal MRI and CSF analysis are crucial for accurate diagnosis and prompt therapeutic intervention, potentially improving long-term outcomes.

## Linked entities

- **Diseases:** Multiple sclerosis (MONDO:0005301), spinal cord syndrome (MONDO:0006995)

## Full-text entities

- **Diseases:** optic neuritis (MESH:D009902), lower limb weakness (MESH:D018908), demyelination (MESH:D003711), lymphocytic pleocytosis (MESH:D007964), sensory deficits (MESH:D012678), spastic paraparesis (MESH:D020336), periventricular lesion (MESH:D054091), MS (MESH:D009103), hyperreflexia (MESH:D012021), Spinal Cord Syndrome (MESH:D013118), brainstem syndromes (MESH:D020295), thoracic pain (MESH:D010146)
- **Chemicals:** methylprednisolone (MESH:D008775)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

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## References

17 references — full list in the complete paper: https://tomesphere.com/paper/PMC12774292/full.md

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Source: https://tomesphere.com/paper/PMC12774292