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
Hauptverfasser: Sahinoglu, M., Mutlukan, A., Koktekir, E., Karabagli, H.
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Sprache:eng
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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.
ISSN:0256-7040
1433-0350
DOI:10.1007/s00381-018-3946-z