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腰椎小关节症状性血肿:脊柱关节卒中?

Symptomatic hematoma of lumbar facet joint: joint apoplexy of the spine?

作者信息

Nishida Kotaro, Iguchi Tetsuhiro, Kurihara Akira, Doita Minoru, Kasahara Koichi, Yoshiya Shinichi

机构信息

Department of Orthopaedic Surgery, Kobe Rosai Hospital, Japan.

出版信息

Spine (Phila Pa 1976). 2003 Jun 1;28(11):E206-8. doi: 10.1097/01.BRS.0000068244.65543.55.

DOI:10.1097/01.BRS.0000068244.65543.55
PMID:12782995
Abstract

STUDY DESIGN

A case report.

OBJECTIVES

To report and discuss a rare case of epidural hematoma that was considered to be formed as a result of idiopathic bleeding occurring at the facet joint (joint apoplexy).

SUMMARY OF THE BACKGROUND DATA

Spontaneous spinal epidural hematoma is a relatively rare condition. According to a review article of 199 spontaneous spinal epidural hematomas in the last 2 decades, the majority of these conditions are thought to result from a rupture of the epidural vascular network. Recently, a hemorrhagic lumbar synovial cyst and a hematoma occurring from the ligamentum flavum were reported as rare types of epidural hematoma.

METHODS

The authors describe the treatment and the clinical, radiologic, surgical, and pathologic findings in one patient with a rare epidural hematoma.

RESULTS

Magnetic resonance imaging revealed that the extradural mass lesion was continuous with the right L4-5 facet joint; this was confirmed by surgery when the extradural hematoma was directly visualized. The joint cavity was also filled with the hematoma. There was no evidence of preceding cyst formation macroscopically or microscopically. The excised capsule of the left L4-5 facet joint revealed moderate hyperplasia of the synovium with an increased number of capillary vessels.

CONCLUSIONS

This is the first reported case of radiculopathy considered to be a result of facet joint apoplexy in the absence of any preceding synovial cyst formation. The pathomechanism of the hemorrhage at the lumbar facet joint is unclear, but it is speculated that there could be an association with degenerative change of the facet joint. Surgical excision of this mass was considered to be the definitive treatment.

摘要

研究设计

病例报告。

目的

报告并讨论一例罕见的硬膜外血肿病例,该血肿被认为是由于小关节突关节特发性出血(关节卒中)所致。

背景资料总结

自发性脊髓硬膜外血肿是一种相对罕见的病症。根据一篇对过去20年中199例自发性脊髓硬膜外血肿的综述文章,这些病症大多被认为是硬膜外血管网破裂所致。最近,有报道称出血性腰椎滑膜囊肿和黄韧带血肿是硬膜外血肿的罕见类型。

方法

作者描述了一例罕见硬膜外血肿患者的治疗情况以及临床、影像学、手术和病理检查结果。

结果

磁共振成像显示硬膜外肿块与右侧L4-5小关节突关节相连;手术时直接观察到硬膜外血肿,证实了这一点。关节腔内也充满了血肿。在宏观和微观上均未发现先前存在囊肿形成的证据。切除的左侧L4-5小关节突关节囊显示滑膜中度增生,毛细血管数量增加。

结论

这是首例报道的在无任何先前滑膜囊肿形成情况下被认为是小关节突关节卒中导致神经根病的病例。腰椎小关节突关节出血的发病机制尚不清楚,但据推测可能与小关节突关节的退行性改变有关。手术切除该肿块被认为是确定性治疗方法。

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