儿童脊髓朗格汉斯细胞组织细胞增生症的治疗:系统回顾

IF 1.7 Q2 SURGERY
Macherla Haribabu Subramaniam, Victor Moirangthem, Muralidharan Venkatesan
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引用次数: 0

摘要

背景:脊柱朗格汉斯细胞组织细胞增生症在儿童中可表现为单发的单灶型或全身型。脊柱单发性组织细胞增生症的治疗方法很多。其中包括病灶自发消退和监督治疗、病灶注射类固醇、全身化疗、放疗和手术。多种选择给治疗专家带来了决策难题。作者试图根据Garg对放射学椎体塌陷的分级,制定脊柱朗格汉斯细胞组织细胞增生症的管理算法:在进行综述时遵循了《系统综述和元分析首选报告项目-2020》指南,并从已建立的医学数据库中筛选了相关研究。在采用严格的纳入和排除标准后,纳入了 2003 年至 2022 年间发表的文章。第一作者和第二作者对筛选出的研究摘要进行了审阅,然后再将其纳入研究。研究已在 Prospero 注册。纳入研究的偏倚评估采用 MINOR 标准:结果:分析了 8 项回顾性系列病例研究。在这些研究中,共有 116 名儿童(平均年龄为 7.4 岁)接受了治疗。平均随访时间为 52.1 个月。在这些患者中,有 37 例肿瘤位于颈椎,40 例位于胸椎,25 例位于腰椎,1 例位于骶骨。研究发现,全身化疗可降低放射性椎体塌陷的风险(P < 0.05)。手术治疗能为伽格 IB 和 II 级脊柱肿瘤患者带来最佳疗效,并能恢复椎体高度(P < 0.05)。没有发现与 III 级相关的病例系列。椎体高度的恢复是表明病变终点或愈合的一个重要放射学参数,通过手术、全身化疗、支具和监护管理可以尽早实现椎体高度的恢复:结论:Garg的IA级肿瘤可首选观察治疗。结论:Garg'sⅠA 级肿瘤可首选观察治疗,ⅠB 和Ⅱ级肿瘤对手术治疗反应良好。III级肿瘤的治疗需要因人而异:C.
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Management of Spinal Langerhans Cell Histiocytosis in Children: A Systematic Review.

Background: Spinal Langerhans cell histiocytosis can manifest as solitary site unifocal form or as systemic form in children. The management options for solitary spinal site unifocal form are many. They include spontaneous resolution of the lesion and supervised treatment, steroid injection of the lesion, systemic chemotherapy, radiation therapy and surgery. Multiple options create a decision-making dilemma for the treating specialist. The authors sought to formulate a management algorithm of spinal Langerhans cell histiocytosis based on Garg's grading of radiographic vertebral body collapse.

Materials and methods: The Preferred Reporting Items for Systematic Reviews and Meta-Analyses-2020 guidelines were followed in conducting the review and studies were filtered from established medical databases. Articles published between 2003 and 2022 were included after applying strict inclusion and exclusion criteria. The first and second authors reviewed the abstracts of filtered studies before including them. The study was registered with Prospero. The bias assessment of included studies was assessed using the MINOR's criteria.

Results: Eight retrospective case series were analyzed. Within these studies, a total of 116 children (mean age 7.4 years) had undergone treatment. The mean follow-up period was 52.1 months. Among these patients, there were 37 tumors in the cervical spine, 40 in the thoracic spine, 25 in the lumbar spine, and a single tumor in the sacrum. Systemic chemotherapy has been found to reduce the risk of radiographic vertebral body collapse (p < 0.05). Surgery provides optimal outcomes in patients with Garg's grade IB , II spinal tumors and restores vertebral body height (p < 0.05). No case series were found pertaining to grade III. Reconstitution of vertebral body height, an important radiological parameter indicating the endpoint or healing of the lesion, was early achieved with surgery followed by systemic chemotherapy, bracing, and supervised management.

Conclusion: Observation can be preferred in Garg's grade IA. Grade IB and II tumors respond well to surgery. Treatment for grade III tumors needs to be tailored on an individual basis.

Grade of recommendation: C.

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来源期刊
CiteScore
3.10
自引率
0.00%
发文量
162
期刊介绍: The International Journal of Spine Surgery is the official scientific journal of ISASS, the International Intradiscal Therapy Society, the Pittsburgh Spine Summit, and the Büttner-Janz Spinefoundation, and is an official partner of the Southern Neurosurgical Society. The goal of the International Journal of Spine Surgery is to promote and disseminate online the most up-to-date scientific and clinical research into innovations in motion preservation and new spinal surgery technology, including basic science, biologics, and tissue engineering. The Journal is dedicated to educating spine surgeons worldwide by reporting on the scientific basis, indications, surgical techniques, complications, outcomes, and follow-up data for promising spinal procedures.
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