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霍奇金淋巴瘤伴脊髓压迫症。一例病例报告及文献综述。

Hodgkin's disease with spinal cord compression. A case report and a review of the literature.

作者信息

Higgins S A, Peschel R E

机构信息

Department of Therapeutic Radiology, Yale University School of Medicine, New Haven, Connecticut 06510.

出版信息

Cancer. 1995 Jan 1;75(1):94-8. doi: 10.1002/1097-0142(19950101)75:1<94::aid-cncr2820750116>3.0.co;2-#.

Abstract

BACKGROUND

Spinal cord compression is a rare complication of Hodgkin's disease, occurring in only 5% of cases, usually in the setting of progressive, advanced disease. As the initial symptom of Hodgkin's disease, it is extremely rare, with only a few cases reported in the literature.

METHODS

A case report of a 46-year-old man who presented with signs and symptoms of spinal cord compression and was found to have an extradural mass in the cervical and thoracic spine is described. Biopsy revealed Hodgkin's disease. This case report represents a unique case of a patient with Hodgkin's disease presenting with epidural disease, with spinal cord compression as the only apparent site of initial clinical involvement. A review of the literature of patients with Hodgkin's disease presenting with spinal cord compression from 1970 to the present is presented.

RESULTS

The patient, whom we report, received chemotherapy followed by external beam radiation therapy and achieved complete resolution of symptoms and a complete response by radiologic criteria. Based on a review of the literature, Hodgkin's disease involving the spinal epidural space is very responsive to radiation therapy and chemotherapy with a good prognosis for both functional recovery (86%), complete response (61%), and long term survival.

CONCLUSIONS

Chemotherapy and/or radiation therapy is successful treatment for Hodgkin's disease presenting with spinal cord compression. For the rare patient who presents with spinal cord compression as the initial symptom of Hodgkin's disease, the therapeutic options include chemotherapy alone, radiation therapy alone, or combined modality therapy.

摘要

背景

脊髓压迫是霍奇金淋巴瘤的一种罕见并发症,仅发生于5%的病例中,通常见于疾病进展期或晚期。作为霍奇金淋巴瘤的首发症状则极为罕见,文献中仅有少数病例报道。

方法

描述了1例46岁男性病例,该患者出现脊髓压迫的体征和症状,经检查发现颈段和胸段脊柱硬膜外有肿块。活检显示为霍奇金淋巴瘤。该病例报告了1例以硬膜外病变为表现的霍奇金淋巴瘤患者,脊髓压迫是唯一明显的初始临床受累部位。本文还对1970年至今出现脊髓压迫的霍奇金淋巴瘤患者的文献进行了综述。

结果

我们报道的该患者接受了化疗,随后进行了外照射放疗,症状完全缓解,影像学检查达到完全缓解标准。根据文献综述,累及脊髓硬膜外间隙的霍奇金淋巴瘤对放疗和化疗反应良好,功能恢复(86%)、完全缓解(61%)及长期生存的预后均较好。

结论

化疗和/或放疗是治疗出现脊髓压迫的霍奇金淋巴瘤的成功方法。对于以脊髓压迫作为霍奇金淋巴瘤首发症状的罕见患者,治疗选择包括单纯化疗、单纯放疗或综合治疗。

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