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◆ Surgical neurology international2026-01-01

Atlantoaxial dislocation in a patient with Neurofibromatosis type 1: Case report and review.

Abolfazl Rahimizadeh, Housain Soufiani, Khodakaram Rastegar, Abdolhadi Daneshi, Chia Peroutighalat, Mahan Amirzadeh, Naser Asgari

一句话结论 · In one sentence

Here, we reviewed the clinical presentation, diagnostic challenges, and surgical fusion for C1-C2 instability in a 65-year-old male with type 1 (NF1) and cervicomedullary cord compression.

原始摘要(英文原文)· Original abstract
BACKGROUND: Neurofibromatosis type 1 (NF1) or von Recklinghausen's disease is a complex multi-system genetic disorder characterized by neurocutaneous manifestations, nervous system affection, and various skeletal dysplasia. Rarely, this disorder might be associated with atlantoaxial dislocation (AAD). CASE DESCRIPTION: A 65-year-old male with a prior diagnosis of (NF1) was referred due to progressive spastic quadriparesis. Dynamic cervical spine radiographs and magnetic resonance showed reducible AAD with cervicomedullary cord compression/myelopathy. Triple construct C1-C2 screw-rod-hook fixation results in steady postoperative neurological recovery. CONCLUSION: Here, we reviewed the clinical presentation, diagnostic challenges, and surgical fusion for C1-C2 instability in a 65-year-old male with type 1 (NF1) and cervicomedullary cord compression.
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Atlantoaxial dislocation in a patient with Neurofibromatosis type 1: Case report and review. — 科研速览 Science Skim