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Ossification of the posterior atlantoaxial membrane associated with atlas hypoplasia: A case report
RATIONALE: Hypoplasia with an intact posterior arch of the atlas and ossification of the posterior atlantoaxial membrane (PAAM) are individually rare. PATIENT CONCERNS: The patient presented with a 6-month history of progressive weakness and paresthesia of his lower extremities. DIAGNOSES: Cervical...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Wolters Kluwer Health
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5134809/ https://www.ncbi.nlm.nih.gov/pubmed/27902623 http://dx.doi.org/10.1097/MD.0000000000005563 |
Sumario: | RATIONALE: Hypoplasia with an intact posterior arch of the atlas and ossification of the posterior atlantoaxial membrane (PAAM) are individually rare. PATIENT CONCERNS: The patient presented with a 6-month history of progressive weakness and paresthesia of his lower extremities. DIAGNOSES: Cervical myelopathy resulting from atlas hypoplasia and ossification of the posterior atlantoaxial membrane. INTERVENTIONS: Laminectomy of the atlas with duroplasty. OUTCOMES: Preoperative symptoms were alleviated. LESSONS: In most reported cases, either atlas hypoplasia or ossification of the PAAM is responsible for patients’ myelopathy. The case illustrated here, to the best of our knowledge, is the first one with coexistent atlas hypoplasia and ossification of the PAAM. And laminectomy of the atlas with duroplasty provided satisfied outcome. |
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