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先天性环状缩窄带:一例伴有假关节形成的病例报告及文献复习

Congenital annular constricting band: a case report with pseudarthrosis and review of the literature.

作者信息

Martinot-Duquennoy V, Bonnevalle M, Herbaux B, Pellerin P, Debeugny P

机构信息

Department of Pediatric Surgery, Huriez Hospital, Lille, France.

出版信息

Eur J Pediatr Surg. 1995 Dec;5(6):380-4. doi: 10.1055/s-2008-1066250.

Abstract

A case of congenital annular constricting band syndrome with an open pseudarthrosis of the tibia and fibula is reported. Ischemia, neurological defect and major lymphoedema were present. The child had an emergency treatment combining an external fixator and a one-stage resection of the constricting band. Bone union was obtained within 4 weeks and complete neurological recovery at 6 months. Long-term result, with realignment and normal function, is satisfactory. A review of the literature is undertaken. Amputations are frequent, however pseudarthroses are rare. One-step treatment of the band has been proposed by certain authors. Neurological recovery is usual. The risk of ischemia favors an early surgical treatment.

摘要

报告了一例先天性环状束带综合征合并胫腓骨开放性假关节的病例。存在缺血、神经功能缺损和严重淋巴水肿。患儿接受了外固定器与一期切除束带相结合的急诊治疗。4周内实现骨愈合,6个月时神经功能完全恢复。长期结果显示,肢体对线和功能正常,效果令人满意。本文对相关文献进行了综述。截肢情况较为常见,但假关节罕见。部分作者提出了对束带进行一步治疗的方法。神经功能恢复较为常见。缺血风险促使早期进行手术治疗。

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