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颈椎戈谢病——病例报告及文献复习

Gorham disease of the cervical spine-a case report and review of the literature.

作者信息

Chong Ng Leslie, Sell Phillip

机构信息

Department of Orthopaedic Surgery, Leicester General Hospital, Leicester, England.

出版信息

Spine (Phila Pa 1976). 2003 Sep 15;28(18):E355-8. doi: 10.1097/01.BRS.0000084557.38858.85.

DOI:10.1097/01.BRS.0000084557.38858.85
PMID:14501935
Abstract

STUDY DESIGN

A case report and literature review of Gorham disease involving the cervical spine.

OBJECTIVES

To describe the clinical course and surgical management of Gorham disease of the cervical spine. The pathologic features and various treatment methods are also discussed.

SUMMARY OF BACKGROUND DATA

Gorham disease is a rare idiopathic disease that possesses distinctive clinical, pathologic, and radiologic features. It is a variant form of osseous angiomatosis associated with massive osteolysis of bone. Eight cases with cervical involvement have been reviewed in the literature and five cases were fatal.

METHODS

We reported a 49-year-old man with Gorham disease of the cervical spine. Repeated surgical attempts to stabilize the cervical spine were required due to progression of the disease.

RESULTS

The patient has achieved a satisfactory functional outcome and remains fully independent.

CONCLUSION

In summary, Gorham disease is a rare entity with an unclear etiology. The long indolent course with the presence of radiographic and pathologic findings usually provides the diagnosis. There is no consensus on treatment, and evaluation of the treatment options is difficult due to the unknown natural history.

摘要

研究设计

一项关于累及颈椎的戈勒姆病的病例报告及文献综述。

目的

描述颈椎戈勒姆病的临床病程及手术治疗情况。同时讨论其病理特征及各种治疗方法。

背景资料总结

戈勒姆病是一种罕见的特发性疾病,具有独特的临床、病理和放射学特征。它是骨血管瘤病的一种变异形式,伴有骨的大量骨质溶解。文献中已回顾了8例累及颈椎的病例,其中5例死亡。

方法

我们报告了一名49岁患有颈椎戈勒姆病的男性患者。由于病情进展,需要反复进行手术以稳定颈椎。

结果

患者获得了满意的功能结果,仍完全独立生活。

结论

总之,戈勒姆病是一种病因不明的罕见疾病。其漫长的隐匿病程以及影像学和病理学表现通常可作出诊断。对于治疗尚无共识,且由于其自然病史未知,难以评估治疗方案。

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Surgical treatment of severe thoracic kyphosis and neurological deficit in a patient with Gorham-Stout syndrome: A case report and literature review.戈谢病-斯托特综合征患者严重胸椎后凸畸形及神经功能缺损的外科治疗:一例报告并文献复习
Front Surg. 2022 Aug 8;9:981025. doi: 10.3389/fsurg.2022.981025. eCollection 2022.
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Rare presentation of angiomatosis in the paranasal sinuses mimicking juvenile nasopharyngeal angiofibroma in a 16 year old male.16岁男性鼻窦血管瘤病罕见表现,酷似青少年鼻咽血管纤维瘤。
Radiol Case Rep. 2022 Jul 29;17(10):3527-3534. doi: 10.1016/j.radcr.2022.07.031. eCollection 2022 Oct.
3
Refractory serositis in Gorham-Stout syndrome.
戈勒姆-斯托特综合征伴难治性浆膜炎。
Orphanet J Rare Dis. 2022 Apr 4;17(1):152. doi: 10.1186/s13023-022-02307-8.
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Current concepts from diagnosis to management in Gorham-Stout disease: a systematic narrative review of about 350 cases.戈勒姆-斯托特病从诊断到治疗的当前概念:对约350例病例的系统叙述性综述
EFORT Open Rev. 2022 Jan 11;7(1):35-48. doi: 10.1530/EOR-21-0083.
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Surgical management of Gorham-Stout syndrome involving the cervical spine with bilateral pleural effusion: A case report and literature review.涉及颈椎并伴有双侧胸腔积液的戈勒姆-斯托特综合征的外科治疗:一例病例报告及文献综述
Exp Ther Med. 2020 Jun;19(6):3851-3855. doi: 10.3892/etm.2020.8627. Epub 2020 Mar 30.
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Spinal Gorham-Stout syndrome: radiological changes and spinal deformities.脊柱戈谢病-斯托特综合征:影像学改变与脊柱畸形
Quant Imaging Med Surg. 2019 Apr;9(4):565-578. doi: 10.21037/qims.2019.03.17.
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Massive Axial and Appendicular Skeletal Deformities in Connection with Gorham-Stout Syndrome.与戈勒姆-斯托特综合征相关的严重轴向和附属骨骼畸形
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Thoracic spine dislocation in Gorham-Stout Syndrome: Case report and literature review.戈勒姆-斯托特综合征中的胸椎脱位:病例报告及文献综述
Surg Neurol Int. 2018 Nov 1;9:223. doi: 10.4103/sni.sni_311_18. eCollection 2018.
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Expert's comment concerning Grand Rounds case entitled "Thoracic osteotomy for Gorham-Stout disease of the spine: a case report and literature review" by C. Maillot et al., Eur Spine J: doi 10.1007/s00586-014-3613-3.专家对C. Maillot等人发表于《欧洲脊柱杂志》(doi: 10.1007/s00586-014-3613-3)题为“脊柱戈谢病的胸椎截骨术:病例报告及文献综述”的大查房病例的评论
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