复杂NF1患儿严重颈椎后凸1例,病例报告及文献复习。

IF 1.3 4区 医学 Q4 CLINICAL NEUROLOGY
Luigi Aurelio Nasto, Ferruccio De Prisco, Enrico Pola, Silverio Perrotta, Giuseppina Miele, Gianluca Piatelli, Claudia Santoro
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引用次数: 0

摘要

目的:我们报告了一名2岁零10个月的1型神经纤维瘤病(NF1)女孩的术前评估、处理和术后随访的详细描述,该患者表现为严重的营养不良、颈椎后凸(170度),并伴有广泛的椎前和椎旁网状神经纤维瘤,该患者也接受了MEK抑制剂治疗。NF1的颈椎后凸特别罕见,在临床放射学特征、手术入路和结果方面没有广泛的文献报道。因此,我们也对有关该主题的现有文献进行了全面审查。方法:通过回顾性分析患者的所有医学文献和影像学资料,进行临床报告。系统评价是根据作者根据系统评价和荟萃分析首选报告项目(PRISMA)制定的NF1患者颈椎后凸手术治疗的纳入和排除标准进行的。结果:我们的患者接受了一期晕重力牵引,随后进行了一期枕颈后路融合术。6周的牵引使畸形从170°减少到90°。通过手术获得了进一步的改善,最终曲率矫正了60%(最后一次术后x线检查为69°)。随访1年半无并发症发生。丛状神经纤维瘤用MEK抑制剂治疗:曲美替尼治疗1年11个月,直到行晕牵引,术后用塞鲁美替尼治疗。根据我们的选择标准,我们只找到了19篇合适的论文。结论:前后路联合融合术(CAP)虽然并不总是可行,但通常是最好的治疗选择。当丛状、有症状、不能手术的神经纤维瘤共存时,手术前或手术后可采用MEK抑制剂治疗,以更好地控制肿瘤或缩小肿瘤体积。最好的治疗选择应该是多学科、专家方法和为患者量身定制的设计的结果。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Severe cervical kyphosis in a complex child with NF1, case report and literature review.

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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来源期刊
Child's Nervous System
Child's Nervous System 医学-临床神经学
CiteScore
3.00
自引率
7.10%
发文量
322
审稿时长
3 months
期刊介绍: The journal has been expanded to encompass all aspects of pediatric neurosciences concerning the developmental and acquired abnormalities of the nervous system and its coverings, functional disorders, epilepsy, spasticity, basic and clinical neuro-oncology, rehabilitation and trauma. Global pediatric neurosurgery is an additional field of interest that will be considered for publication in the journal.
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