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自发性脊髓硬膜外血肿伴脊髓受压并发浆细胞骨髓瘤。病例报告。

Spontaneous spinal epidural hematoma with spinal cord compression complicating plasma cell myeloma. A case report.

作者信息

Hayem G, Deutsch E, Roux S, Palazzo E, Grossin M, Meyer O

机构信息

Service de Rhumatologie, CHU Bichat-Claude Bernard, Paris, France.

出版信息

Spine (Phila Pa 1976). 1998 Nov 15;23(22):2432-5. doi: 10.1097/00007632-199811150-00015.

DOI:10.1097/00007632-199811150-00015
PMID:9836358
Abstract

STUDY DESIGN

A case is reported in which a patient had acute paraplegia with sensory loss caused by a spontaneous epidural hematoma that was ascribed to bleeding of pre-existing myeloma lesions of the thoracic vertebrae.

OBJECTIVES

To highlight the causes of secondary epidural hematomas with special attention to pre-existing vertebral or epidural lesions.

SUMMARY OF BACKGROUND DATA

There are no apparent previous reports of epidural spinal hematomas ascribed to underlying malignant diseases. Benign dysplasia, such as hemangioma or Paget's disease, has been implicated in a few cases.

METHODS

A case of spontaneous dorsal epidural hematoma is reported in a patient followed up for plasma cell myeloma with osteolytic lesions in the lower thoracic spine. There was no history of major trauma or coagulation disorders. Complete loss of motor and sensory function in both lower limbs was noted, with sphincter dysfunction. Magnetic resonance imaging of the thoracic spine showed a large posterolateral epidural hematoma responsible for spinal cord compression.

RESULTS

The patient failed to improve despite surgical decompression within 6 hours of symptom onset. He died 13 days later of refractory bacterial pneumonia. A large epidural hematoma adjacent to myelomatous lesions of the thoracic vertebrae was found at autopsy.

CONCLUSIONS

This is the first reported case of spontaneous epidural hematoma ascribed to underlying malignant disease, with confirmation of the diagnosis by postmortem examination. Possible mechanisms include tumor-related epidural inflammation and fragility of epidural venous plexuses.

摘要

研究设计

报告一例患者,其因自发性硬膜外血肿导致急性截瘫并伴有感觉丧失,该血肿归因于胸椎先前存在的骨髓瘤病变出血。

目的

强调继发性硬膜外血肿的病因,特别关注先前存在的椎体或硬膜外病变。

背景资料总结

以前没有明显的关于硬膜外脊髓血肿归因于潜在恶性疾病的报道。良性发育异常,如血管瘤或佩吉特病,在少数病例中被认为与之有关。

方法

报告一例自发性背部硬膜外血肿病例,该患者因浆细胞骨髓瘤接受随访,下胸椎有溶骨性病变。无重大创伤或凝血障碍病史。注意到双下肢运动和感觉功能完全丧失,并伴有括约肌功能障碍。胸椎磁共振成像显示一个巨大的后外侧硬膜外血肿,导致脊髓受压。

结果

尽管在症状出现后6小时内进行了手术减压,但患者病情仍未改善。他在13天后死于难治性细菌性肺炎。尸检发现胸椎骨髓瘤病变附近有一个巨大的硬膜外血肿。

结论

这是首例报告的归因于潜在恶性疾病的自发性硬膜外血肿病例,并通过尸检证实了诊断。可能的机制包括肿瘤相关的硬膜外炎症和硬膜外静脉丛的脆弱性。

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