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Management of delayed Sprengel malformation with intracanalar compressive omovertebral bone in a developing country's neurosurgery unit.发展中国家神经外科单位中管内压迫性骨桥导致的延迟性 Sprengel 畸形的处理。
BMJ Case Rep. 2021 Jun 28;14(6):e243203. doi: 10.1136/bcr-2021-243203.
2
Cervical myelopathy secondary to omovertebral bone in the pediatric patient with Sprengel deformity.小儿 Sprengel 畸形患者中因移行椎骨导致的颈椎脊髓病。
Neurosciences (Riyadh). 2021 Jan;26(1):89-92. doi: 10.17712/nsj.2021.1.20200040.
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The congenital undescended scapula syndrome: Sprengel and the cleithrum: a case series and hypothesis.先天性肩胛骨发育不全综合征:Sprengel 畸形与喙突:病例系列与假说。
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Bilateral Sprengel Deformity With Bilateral Omovertebral Bone: An Unusual Case in an Adult Patient: A Case Report.双侧先天性高肩胛症合并双侧肩胛上移骨:一例成人患者的罕见病例:病例报告
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Trapezius sparing minimally aggressive surgical technique for sprengel deformity: A case report.保留斜方肌的微创治疗先天性高肩胛症手术技术:病例报告
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Sprengel Deformity in Biological Sisters.生物姐妹中的 Sprengel 畸形。
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Correction in malrotation of the scapula and muscle transfer for the management of severe Sprengel deformity: static and dynamic evaluation using 3-dimensional computed tomography.肩胛骨旋转不良矫正及肌肉转移治疗重度先天性高肩胛症:基于三维计算机断层扫描的静态和动态评估
J Pediatr Orthop. 2013 Mar;33(2):205-11. doi: 10.1097/BPO.0b013e318279c656.

本文引用的文献

1
Congenital high scapula (Sprengel's deformity): four cases.先天性高肩胛(斯普林格尔畸形):四例报告。
Diagn Interv Imaging. 2012 Nov;93(11):878-83. doi: 10.1016/j.diii.2012.08.006. Epub 2012 Oct 16.
2
Sprengel deformity: pathogenesis and management.Sprengel 畸形:发病机制与治疗。
J Am Acad Orthop Surg. 2012 Mar;20(3):177-86. doi: 10.5435/JAAOS-20-03-177.
3
Previously unreported structure associated with Sprengel deformity.与先天性高肩胛症相关的此前未报道过的结构。
J Pediatr Orthop. 2009 Jan-Feb;29(1):26-8. doi: 10.1097/BPO.0b013e3181919505.
4
Developmental anomalies of the scapula-the "omo"st forgotten bone.肩胛骨的发育异常——最易被遗忘的“肩胛”骨。
Am J Med Genet A. 2003 Aug 1;120A(4):583-7. doi: 10.1002/ajmg.a.20091.
5
[Congenital elevation of the scapula in children. Anatomo-pathological and therapeutic study apropos of 27 cases].[儿童先天性高肩胛症。关于27例的解剖病理学及治疗研究]
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发展中国家神经外科单位中管内压迫性骨桥导致的延迟性 Sprengel 畸形的处理。

Management of delayed Sprengel malformation with intracanalar compressive omovertebral bone in a developing country's neurosurgery unit.

机构信息

Neurosurgery, USTTB, Bamako, Mali

Neurosurgery, Mere Enfant Hospital, Bamako, Mali.

出版信息

BMJ Case Rep. 2021 Jun 28;14(6):e243203. doi: 10.1136/bcr-2021-243203.

DOI:10.1136/bcr-2021-243203
PMID:34183314
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8240559/
Abstract

Sprengel deformity is a congenital abnormality done to the ascent of the scapular bone (which occurs probably between the 5th and 12th weeks of gestation). It can cause cosmetic or functional problems. The aim of our study was to describe this rare deformity, often neglected in our context, and its surgical management. We report a case of a 16-year-old boy with a Sprengel deformity associated with omovertebral intracanalar compressive bone seen on the CT scan. He reported neurological symptoms such as spastic paraparesis and walk disturbances. The bone was resected surgically and physiotherapy was set up. The outcome was good with noticeable neurological improvement of walk and balance, recovery of autonomy. Sprengel deformity is a rare pathology. Surgery must be done early and be adapted to the case.

摘要

肩胛高耸症是一种先天性肩胛骨上升畸形(可能发生在妊娠第 5 至 12 周之间)。它会导致美容或功能问题。我们的研究目的是描述这种在我们的背景下经常被忽视的罕见畸形及其手术治疗。我们报告了一例 16 岁男孩的病例,该男孩患有肩胛高耸症,伴有 CT 扫描所见的过顶椎椎管内压迫性骨。他报告有神经症状,如痉挛性截瘫和行走障碍。通过手术切除了骨头,并进行了物理治疗。结果良好,行走和平衡的神经功能明显改善,恢复了自主性。肩胛高耸症是一种罕见的疾病。手术必须尽早进行,并根据具体情况进行调整。