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Marburg MS case shows treatment challenges and fatal outcome

Marburg MS case shows treatment challenges and fatal outcome
Photo by Adam Winger / Unsplash
Key Takeaway
Aggressive Marburg MS can be fatal despite multi-therapy escalation, highlighting need for timely, individualized care.

A 46-year-old woman with the Marburg variant of multiple sclerosis presented with severe, rapidly progressive disease. Initial treatment with corticosteroids, plasmapheresis, and intravenous immunoglobulin failed to control her lesions, leading to a switch to high-dose cyclophosphamide. This provided radiologic stabilization but was severely limited by the development of refractory cytopenia.

The patient was then transitioned from ocrelizumab to subcutaneous ofatumumab, but her clinical course rapidly deteriorated. She experienced recurrent aspiration events and significant functional decline, ultimately resulting in death. This case underscores the extreme aggressiveness of Marburg MS and the narrow therapeutic window for effective intervention.

The report highlights critical therapeutic challenges, including treatment-limiting toxicities like cytopenia and logistical barriers to administering anti-CD20 therapies. It emphasizes the need for timely, individualized immunosuppressive strategies in such aggressive presentations. The case serves as a stark reminder of the potential for fatal outcomes despite aggressive treatment escalation.

Limitations include the single-case design, which limits generalizability. However, the detailed clinical course provides valuable insight into managing this rare and severe MS variant. The findings stress the importance of early, aggressive intervention while carefully monitoring for adverse events.

Study Details

Study typeSystematic review
EvidenceLevel 1
PublishedMay 2026
View Original Abstract ↓
Marburg variant of multiple sclerosis (MS) is a rare, fulminant demyelinating disorder characterized by rapid neurological decline and notable lack of established standardized treatment guidelines. We describe a 46-year-old woman presenting with progressive cognitive and behavioral changes and multifocal CNS lesions initially refractory to corticosteroids, plasmapheresis (PLEX), and intravenous immunoglobulin (IVIg). Brain biopsy confirmed aggressive MS-spectrum demyelination. Escalation to high-dose cyclophosphamide resulted in radiologic stabilization but was limited by severe, refractory cytopenia. Given persistent disease activity and intolerance to infusion-based therapy, transition from ocrelizumab to subcutaneous ofatumumab was planned as a pragmatic maintenance strategy; however, treatment initiation was delayed. The patient subsequently experienced rapid clinical deterioration marked by recurrent aspiration events and functional decline, ultimately leading to death following transition to comfort-focused care. This case highlights the therapeutic challenges of Marburg MS, including treatment-limiting toxicity, logistical barriers to anti-CD20 therapy, and the critical importance of timely, individualized immunosuppressive strategies.
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