Cauda equina syndrome in a patient diagnosed with type 1 Gaucher disease: a rare case
Background Gaucher disease is a rare hereditary glycolipid storage disease. One of the rare complications is neurodeficits due to vertebral involvement. Case presentation An 18-year-old female patient presented to the outpatient clinic with cauda equina syndrome due to sacral involvement of type 1 G...
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Veröffentlicht in: | Child's nervous system 2019-01, Vol.35 (1), p.191-194 |
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Hauptverfasser: | , , , |
Format: | Artikel |
Sprache: | eng |
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Online-Zugang: | Volltext |
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Zusammenfassung: | Background
Gaucher disease is a rare hereditary glycolipid storage disease. One of the rare complications is neurodeficits due to vertebral involvement.
Case presentation
An 18-year-old female patient presented to the outpatient clinic with cauda equina syndrome due to sacral involvement of type 1 GD. Bilateral laminectomy via posterior approach without posterior stabilization was performed.
Conclusion
Maximum excision of the mass avoiding destabilization of the spinal column can provide long-term vertebral stability and improvement in neurodeficits. |
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ISSN: | 0256-7040 1433-0350 |
DOI: | 10.1007/s00381-018-3946-z |