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小儿椎间盘钙化:病例系列及文献系统回顾。

Pediatric intervertebral disc calcification: case series and systematic review of the literature.

机构信息

Clinical Orthopedics, Department of Clinical and Molecular Science, School of Medicine, Marche Polytechnic University.

Clinic of Adult and Paediatric Orthopaedic, Ancona United Hospitals, Ancona, Italy.

出版信息

J Pediatr Orthop B. 2020 Nov;29(6):590-598. doi: 10.1097/BPB.0000000000000638.

Abstract

Pediatric intervertebral disc calcification (PIDC) is an uncommon disease with an unclear etiology. The clinical picture may suggest a severe spinal disease, thus involving an extensive differential diagnosis. The aim of this study was to find a diagnostic and treatment approach for PIDC on the basis of the literature. The Medline, Embase, Web of Science, and Cochrane Systematic Review databases were searched for relevant studies, whose reference lists were checked manually for additional articles. For each study, year of publication, study design, demographics, onset type, history of trauma, clinical and neurological signs and symptoms, imaging studies performed, blood test results, treatment strategies, and outcomes were recorded. The charts of eight patients with symptomatic PIDC treated at our institution from 2000 to 2016 were reviewed. Of 1522 articles identified by the search, 51 level IV studies involving 91 patients fulfilled the inclusion criteria. Most patients were treated conservatively and achieved complete recovery. Of the 13 patients who were treated surgically, one had a persistent myelopathy at the final follow-up. All the patients of our case series were treated conservatively and achieved complete symptom resolution at the final follow-up. PIDC is predominantly a benign and self-limiting condition. Surgery should be considered only in case of failure of conservative treatment in the presence of severe neurological impairment and myelopathy. Level of Evidence: IV (case series and systematic review of level IV studies).

摘要

小儿椎间盘钙化(PIDC)是一种病因不明的罕见疾病。临床表现可能提示严重的脊柱疾病,因此需要广泛的鉴别诊断。本研究旨在根据文献为 PIDC 找到一种诊断和治疗方法。我们检索了 Medline、Embase、Web of Science 和 Cochrane 系统评价数据库,以查找相关研究,并手动检查其参考文献以获取其他文章。对于每一项研究,我们记录了发表年份、研究设计、人口统计学、发病类型、创伤史、临床和神经体征和症状、进行的影像学研究、血液检查结果、治疗策略和结果。回顾了 2000 年至 2016 年在我院接受治疗的 8 例有症状 PIDC 患者的病历。通过检索共确定了 1522 篇文章,其中 51 项 IV 级研究涉及 91 例患者符合纳入标准。大多数患者接受保守治疗并完全康复。在接受手术治疗的 13 例患者中,有 1 例在最终随访时仍存在持续性脊髓病。我们的病例系列中的所有患者均接受保守治疗,在最终随访时完全缓解症状。PIDC 主要是一种良性和自限性疾病。只有在存在严重神经功能障碍和脊髓病且保守治疗失败的情况下,才应考虑手术。证据等级:IV(病例系列和 IV 级研究的系统评价)。

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