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脊柱原发性 B 淋巴细胞性淋巴瘤孤立表现:系统文献复习并结合病例举例。

Solitary manifestations of primary B-lymphoblastic lymphoma of the spine: Systematic literature review with case illustration.

机构信息

Department of Neurosurgery, Clinical Neurosciences Center, University of Utah, 175N Medical Drive East, Salt Lake City, UT 84132, USA.

Department of Neurosurgery, Clinical Neurosciences Center, University of Utah, 175N Medical Drive East, Salt Lake City, UT 84132, USA.

出版信息

Clin Neurol Neurosurg. 2022 Jan;212:107064. doi: 10.1016/j.clineuro.2021.107064. Epub 2021 Nov 24.

Abstract

BACKGROUND

Given the locally destructive osteolytic nature of primary B-cell lymphoblastic lymphoma (B-LBL) of the spine, careful attention is needed to identify clinical signs and symptoms as well as radiological findings of spinal instability because these lesions may warrant resection, decompression, and instrumentation with posterolateral fusion. Our objective was to summarize the presenting symptoms, clinical features, potential treatment modalities, and clinical outcome of cases described in the literature.

METHODS

We undertook a systematic literature review to identify all relevant cases and case series describing primary manifestations B-LBL of the spine using Pubmed/Medline. We summarized the findings in accordance with the PRISMA guidelines. We also present a case illustration.

RESULTS

Together with our case, 9 cases of primary B-LBL of the spine were identified in 6 male and 3 female patients (age 8-58 years, median 31 years). Back pain was the most common symptom, and five patients also had neurological signs of spinal cord compression. T1-weighted MRI contrast enhancement was seen in 5 cases. Surgery was performed in 5 patients with progression of neurological deficits. Steroid treatment was also given in 3 patients preoperatively. Seven patients had chemotherapy after diagnosis. During follow-up of 1 month to 1 year, 2 cases of recurrence and 4 cases of complete remission were noted; however, with the short follow-up time, patient prognosis overall remains unclear.

CONCLUSIONS

Primary B-LBL of the spine represents a rare clinical entity whose management mandates a multidisciplinary approach. Careful attention must be paid to the neurological status of the patient, as well as to imaging that may highlight potential local instability of the spine.

摘要

背景

鉴于原发性 B 细胞淋巴母细胞淋巴瘤(B-LBL)在脊柱处具有局部破坏性溶骨性性质,因此需要仔细注意识别脊柱失稳的临床症状和体征以及影像学发现,因为这些病变可能需要进行切除、减压和器械固定后外侧融合。我们的目的是总结文献中描述的病例的临床表现、潜在治疗方式和临床结果。

方法

我们采用系统文献回顾的方法,使用 Pubmed/Medline 识别所有描述原发性脊柱 B-LBL 表现的相关病例和病例系列。我们按照 PRISMA 指南总结了研究结果。我们还提供了一个病例示例。

结果

连同我们的病例,共在 6 名男性和 3 名女性患者(年龄 8-58 岁,中位数 31 岁)中发现了 9 例原发性脊柱 B-LBL。最常见的症状是背痛,5 例患者还存在脊髓压迫的神经体征。5 例患者的 T1 加权 MRI 对比增强可见。5 例出现神经功能缺损进展的患者进行了手术。3 例患者在术前进行了类固醇治疗。诊断后,7 例患者接受了化疗。在 1 个月至 1 年的随访期间,2 例患者复发,4 例患者完全缓解;然而,由于随访时间较短,患者的总体预后仍不清楚。

结论

原发性脊柱 B-LBL 是一种罕见的临床实体,其治疗需要多学科方法。必须密切关注患者的神经状态,以及可能突出脊柱潜在局部不稳定的影像学检查。

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