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Severe cervical kyphosis in a complex child with NF1, case report and literature review
Luigi Aurelio Nasto1, Ferruccio De Prisco2, Enrico Pola1
1Department of Orthopaedics, "Luigi Vanvitelli" University Hospital, University of Campania "Luigi Vanvitelli", Via del Sole 10, 80138, Naples, Italy.
Insights
This study details the successful surgical and MEK inhibitor treatment of severe cervical kyphosis in a child with neurofibromatosis 1 (NF1). The approach combined traction, fusion, and targeted therapy, achieving significant deformity correction and tumor management.
Area of Science:
- Pediatric Orthopedics
- Neurosurgery
- Medical Genetics
Background:
- Cervical kyphosis in neurofibromatosis 1 (NF1) is rare and presents unique management challenges.
- Plexiform neurofibromas associated with NF1 can exacerbate spinal deformities.
Purpose of the Study:
- To describe the pre-operative assessment, management, and post-operative follow-up of a pediatric patient with NF1 and severe cervical kyphosis.
- To review the literature on the surgical management of cervical kyphosis in NF1 patients.
Main Methods:
- Retrospective review of clinical and imaging data for a single pediatric patient.
- Systematic literature review following PRISMA guidelines for surgical management of cervical kyphosis in NF1.
Main Results:
- A 2-year-old girl with 170° cervical kyphosis underwent halo-gravity traction, reducing the curve to 90°, followed by occipito-cervical fusion achieving 60% correction.
- Plexiform neurofibromas were managed with MEK inhibitors (trametinib and selumetinib), with no observed complications at 1.5-year follow-up.
- A systematic review identified 19 relevant studies on the surgical management of cervical kyphosis in NF1.
Conclusions:
- Combined anterior and posterior fusion is often optimal but not always feasible for cervical kyphosis in NF1.
- MEK inhibitor therapy can be crucial for managing coexisting plexiform neurofibromas, either before or after surgery.
- A multidisciplinary, tailored approach is essential for optimal therapeutic outcomes in complex NF1 cases.
Purpose:
We faced and herein report a detailed description of pre-operative assessment, management, and post-operative follow-up of a 2-year and 10-month-old girl with neurofibromatosis 1 (NF1) who presented with severe, dystrophic, cervical kyphosis (170 degrees) associated with extensive pre- and para-vertebral plexiform neurofibromas, who also went under MEK inhibitors therapy. Cervical kyphosis in NF1 is particularly rare, and there is no extensive literature available on the subject in terms of clinico-radiological features, surgical approach, and outcomes. We therefore also performed a comprehensive review of the available literature on the topic.
Methods:
The clinical report was made through the retrospective review of all medical documents and imaging of the patient. The systematic review was performed based on the inclusion and exclusion criteria set by the authors on surgical management of cervical kyphosis in NF1 patients according to the Preferred Reporting Items for Systematic Reviews and Meta-Analyses (PRISMA).
Results:
Our patient underwent a first-stage halo-gravity traction followed by a single-stage occipito-cervical posterior fusion. The six-week traction resulted in a reduction of the deformity from 170 to 90°. A further amelioration was obtained by surgery with a final 60% correction of the curvature (69° at last post-operative X-ray). No complications were observed at 1-and-a-half-year follow-up. The plexiform neurofibromas were treated with MEK inhibitors: trametinib for 1 year and 11 months until performing halo traction, and with selumetinib after surgery. We just found 19 papers suitable according to our selection criteria.
Conclusion:
Combined anterior and posterior fusion (CAP) is generally the best treatment option, although it is not always feasible. When plexiform, symptomatic, inoperable neurofibromas coexist, surgery can be preceded or followed by MEK inhibitor treatment for better control or a volumetric reduction of the tumors. The best therapeutic choice should always be the result of a multidisciplinary, expert approach and patient-tailored design.
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