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孤立性原发性脊柱结外霍奇金淋巴瘤:病例报告。

Isolated, primary extranodal Hodgkin's disease of the spine: case report.

作者信息

Citow J S, Rini B, Wollmann R, Macdonald R L

机构信息

Department of Surgery, University of Chicago Medical Center, Illinois 60637, USA.

出版信息

Neurosurgery. 2001 Aug;49(2):453-6; discussion 456-7. doi: 10.1097/00006123-200108000-00037.

Abstract

OBJECTIVE AND IMPORTANCE

To describe an unusual case of isolated, primary spinal Hodgkin's disease to draw attention to this disease as a possible diagnosis in patients with mixed inflammatory cell infiltrate lesions located in the spine.

CLINICAL PRESENTATION

A 54-year-old African American woman presented with back pain and progressive lower-extremity weakness as a result of spinal cord compression from Hodgkin's disease of the thoracic vertebrae.

INTERVENTION

The patient underwent decompressive surgery with stabilization, then was incorrectly treated with antituberculosis medication. When the disease progressed, later investigations revealed Hodgkin's disease, which responded to a course of radiation therapy. An extensive examination failed to detect lymphoma elsewhere.

CONCLUSION

Isolated, primary extranodal Hodgkin's disease of the spine is extremely rare. Seven other cases were reported in 1954. Although the Hodgkin's disease in these cases may arise in the bone of the spine, the possibility of origin in the paraspinous soft tissues also cannot be excluded.

摘要

目的及重要性

描述一例罕见的孤立性原发性脊柱霍奇金病病例,以引起对该病的关注,使其成为脊柱混合性炎性细胞浸润病变患者的一种可能诊断。

临床表现

一名54岁的非裔美国女性因胸椎霍奇金病导致脊髓受压,出现背痛和进行性下肢无力。

干预措施

患者接受了减压手术并进行了固定,随后接受了错误的抗结核药物治疗。当病情进展时,后续检查发现了霍奇金病,对一个疗程的放射治疗有反应。全面检查未在其他部位发现淋巴瘤。

结论

孤立性原发性脊柱结外霍奇金病极为罕见。1954年还报道了其他7例。虽然这些病例中的霍奇金病可能起源于脊柱骨,但也不能排除起源于椎旁软组织的可能性。

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