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骶骨骨软骨瘤:一例病例报告及文献综述

Osteochondroma of the sacrum: a case report and review of the literature.

作者信息

Samartzis Dino, Marco Rex A W

机构信息

Graduate Division, Harvard University, Cambridge, MA, USA.

出版信息

Spine (Phila Pa 1976). 2006 Jun 1;31(13):E425-9. doi: 10.1097/01.brs.0000220222.63828.d3.

Abstract

STUDY DESIGN

A case report and review of the literature.

OBJECTIVES

To describe the en bloc excision and postoperative outcome of an osteochondroma of the sacrum compressing the neural elements, as well as review the literature on solitary osteochondroma involving the sacrum.

SUMMARY OF BACKGROUND DATA

Osteochondroma is the most common primary benign bone tumor. However, this tumor rarely involves the spine and even more rarely involves the sacrum. To the best of our knowledge, en bloc excision of a solitary osteochondroma of the sacrum has not been previously reported.

METHODS

An 11-year-old male presented with disabling radicular pain in the right lower extremity. Radiologic studies showed a lesion occurring from the sacral lamina that was compressing the S2 nerve root. The tumor was excised en bloc through a posterior approach. The cavitary defect within the sacrum was reconstructed with crushed cancellous allograft and demineralized bone matrix putty. A literature review of solitary sacral osteochondroma was conducted of the English-based medical literature.

RESULTS

Histologic studies showed the tumor to be an osteochondroma. After surgery, pain was completely relieved, and neurologic function was normal. At the last follow-up, the sacroiliac joint remained intact, and there was no evidence of local recurrence. A literature review revealed 4 previous cases addressing osteochondroma of the sacrum.

CONCLUSIONS

Osteochondroma is a rare primary benign bone tumor that can occur in the sacrum. Local contamination and, therefore, the likelihood of local recurrence, are decreased when an en bloc, as opposed to an intralesional, excision is performed.

摘要

研究设计

病例报告及文献综述。

目的

描述压迫神经组织的骶骨骨软骨瘤的整块切除及术后结果,并复习有关累及骶骨的孤立性骨软骨瘤的文献。

背景资料总结

骨软骨瘤是最常见的原发性良性骨肿瘤。然而,这种肿瘤很少累及脊柱,更罕见累及骶骨。据我们所知,此前尚未报道过骶骨孤立性骨软骨瘤的整块切除。

方法

一名11岁男性因右下肢严重放射性疼痛就诊。影像学检查显示病变起源于骶椎板,压迫S2神经根。通过后路整块切除肿瘤。骶骨内的空洞性缺损用碎松质骨同种异体骨和脱矿骨基质糊剂重建。对基于英文的医学文献进行了关于孤立性骶骨骨软骨瘤的文献综述。

结果

组织学检查显示肿瘤为骨软骨瘤。手术后,疼痛完全缓解,神经功能正常。在最后一次随访时,骶髂关节保持完整,无局部复发迹象。文献综述发现了4例先前报道的骶骨骨软骨瘤病例。

结论

骨软骨瘤是一种可发生于骶骨的罕见原发性良性骨肿瘤。与病灶内切除相比,进行整块切除可减少局部污染,从而降低局部复发的可能性。

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