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Segmental spinal dysgenesis with open spinal dysraphism and Chiari II features, case report
Segmental spinal dysgenesis (SSD) is a complex spinal anomaly characterized by localized dysgenesis of the lumbar or thoracolumbar spine, and severe congenital kyphosis or kyphoscoliosis. We describe a newborn who presented with severe congenital paraplegia and a lumbar mass. Magnetic resonance imag...
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Elsevier
2020
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7452077/ https://www.ncbi.nlm.nih.gov/pubmed/32874392 http://dx.doi.org/10.1016/j.radcr.2020.07.058 |
Sumario: | Segmental spinal dysgenesis (SSD) is a complex spinal anomaly characterized by localized dysgenesis of the lumbar or thoracolumbar spine, and severe congenital kyphosis or kyphoscoliosis. We describe a newborn who presented with severe congenital paraplegia and a lumbar mass. Magnetic resonance imaging confirmed SSD type II associated with open spinal dysraphism and intracranial Chiari II features; this association has not been reported. The association modifies the disease management and outcome. The previous classification of SSD could be revisited based on our case. |
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