Abstract
Stiff person syndrome (SPS) is a rare, debilitating neurological illness characterised by rigidity and spasms of the axial muscles, causing severe restrictions to mobility. SPS can be classic, partial or paraneoplastic. We report a case of a young woman who presented with seizures and painful spasms of the thoracolumbar muscles who was subsequently diagnosed with SPS. Serological work revealed glutamic acid decarboxylase (GAD) antibodies and imaging showed a large mediastinal mass. The patient underwent surgical resection of the mediastinal mass and final pathology revealed well-differentiated mediastinal liposarcoma. She received five sessions of plasma exchange and her neurological symptoms gradually improved after surgery. This case highlights a rare case of GAD antibody-positive paraneoplastic SPS associated with mediastinal liposarcoma.
| Original language | English (US) |
|---|---|
| Article number | e250639 |
| Journal | BMJ case reports |
| Volume | 15 |
| Issue number | 7 |
| DOIs | |
| State | Published - Jul 1 2022 |
| Externally published | Yes |
Bibliographical note
Publisher Copyright:© BMJ Publishing Group Limited 2022. No commercial re-use. See rights and permissions. Published by BMJ.
UN SDGs
This output contributes to the following UN Sustainable Development Goals (SDGs)
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SDG 3 Good Health and Well-being
Keywords
- Cancer
- Cancer intervention
- Malignant disease and immunosuppression
- Movement disorders (other than Parkinsons)
- Neurology
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