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本文引用的文献

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Pure spinal epidural cavernous hemangioma.单纯性脊髓硬膜外海绵状血管瘤。
Acta Neurochir (Wien). 2012 Apr;154(4):739-45. doi: 10.1007/s00701-012-1295-3. Epub 2012 Feb 25.
2
Dorsal spinal epidural cavernous hemangioma.脊髓背侧硬膜外海绵状血管瘤。
J Craniovertebr Junction Spine. 2010 Jul;1(2):122-5. doi: 10.4103/0974-8237.77677.
3
Management of symptomatic vertebral hemangioma: follow-up of 6 patients.有症状椎体血管瘤的治疗:6例患者的随访
J Spinal Disord Tech. 2011 May;24(3):196-201. doi: 10.1097/BSD.0b013e3181e489df.
4
A case of a spinal epidural capillary hemangioma: case report.椎管硬膜外毛细血管瘤 1 例:病例报告。
Neurosurgery. 2011 Mar;68(3):E850-3. doi: 10.1227/NEU.0b013e3182093320.
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Microsurgical resection of cavernous haemangioma around the thoracic neuroforamen: a case report.
J Orthop Surg (Hong Kong). 2010 Dec;18(3):370-3. doi: 10.1177/230949901001800324.
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Vascular causes of radiculopathy: a literature review.血管性神经根病的病因:文献综述。
Spine J. 2011 Jan;11(1):73-85. doi: 10.1016/j.spinee.2010.09.027.
7
Outcome after microsurgery in 14 patients with spinal cavernomas and review of the literature.14 例脊髓海绵状血管畸形患者的显微手术治疗结果及文献复习。
J Neurosurg Spine. 2010 Oct;13(4):524-34. doi: 10.3171/2010.4.SPINE09986.
8
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9
Spinal epidural haemangioma associated with extensive gastrointestinal haemangiomas. A case report.脊髓硬膜外血管瘤合并广泛胃肠道血管瘤:一例报告
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脊柱硬膜外血管瘤的临床与影像学表现:一家三级医疗中心10年期间的临床系列研究

Clinical and radiological presentation of spinal epidural haemangiomas: clinical series in a tertiary care centre during a 10-year period.

作者信息

Mühmer Mario, Bostelmann Richard, Sarikaya-Seiwert Sevgi, Schneiderhan Marcel, Steiger Hans-Jakob, Cornelius Jan Frederick

机构信息

Department of Neurosurgery, Heinrich-Heine-University, Moorenstrasse 5, 40225, Düsseldorf, Germany,

出版信息

Eur Spine J. 2014 Feb;23(2):404-10. doi: 10.1007/s00586-013-3045-5. Epub 2013 Oct 6.

DOI:10.1007/s00586-013-3045-5
PMID:24097259
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3906447/
Abstract

PURPOSE

Haemangiomas are very frequent benign spinal tumours. However, pure epidural location is extremely rare. At present, only 52 cases have been reported in the literature during the last 10 years. We proposed to analyse clinical and radiological features of this rare entity treated in a tertiary care centre over the last 10 years.

METHODS

A study of a retrospective surgical series (2002-2012) was conducted. The clinic's electronic database was searched for "spinal" and/or "vertebral haemangiomas", which were treated by surgery and/or vertebroplasty. Clinical, radiological and histopathological data were analysed.

RESULTS

In total, the series comprised 30 spinal haemangiomas. There were 6 epidural (20 %), 17 vertebral (57 %) and 7 intradural lesions (23 %). There were four men and two women, mean age 28.3 years, with epidural lesions. One patient presented with localised back pain only, two with radiculopathy and focal neurological deficit, two with radiculopathy only and one with isolated focal neurological deficit, respectively. The onset of symptoms was progressive in four cases over weeks to months and sudden in two cases. Preoperative MRI imaging revealed features of meningioma, neurinoma or metastasis.

CONCLUSION

Epidural haemangiomas are extremely rare spinal lesions. They may mimic more common spinal tumours clinically and radiologically. The usual treatment is gross total resection confirming the diagnosis histologically.

摘要

目的

血管瘤是非常常见的脊柱良性肿瘤。然而,单纯硬膜外血管瘤极为罕见。目前,过去10年文献中仅报道了52例。我们旨在分析过去10年在一家三级医疗中心治疗的这种罕见疾病的临床和放射学特征。

方法

对一个回顾性手术系列(2002 - 2012年)进行研究。在该诊所的电子数据库中搜索接受手术和/或椎体成形术治疗的“脊柱”和/或“椎体血管瘤”。分析临床、放射学和组织病理学数据。

结果

该系列共有30例脊柱血管瘤。其中硬膜外6例(20%),椎体17例(57%),硬膜内7例(23%)。硬膜外病变患者中男性4例,女性2例,平均年龄28.3岁。1例仅表现为局部背痛,2例伴有神经根病和局灶性神经功能缺损,2例仅伴有神经根病,1例仅伴有孤立的局灶性神经功能缺损。4例患者症状在数周数月内逐渐出现,2例为突然出现。术前MRI成像显示有脑膜瘤、神经鞘瘤或转移瘤的特征。

结论

硬膜外血管瘤是极为罕见的脊柱病变。它们在临床和放射学上可能类似更常见的脊柱肿瘤。通常的治疗方法是进行全切除,并通过组织学检查确诊。