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原发性脊髓内淋巴瘤早期诊断要点。如何早期怀疑原发性脊髓内淋巴瘤并进行侵入性活检?一例病例报告及文献综述。

Essentials for early diagnosis of primary intramedullary spinal cord lymphoma. How to suspect primary intramedullary spinal cord lymphoma early and proceed to invasive biopsy? A case report and literature review.

作者信息

Shigekawa Seiji, Inoue Akihiro, Miyazaki Yukihiro, Taniwaki Mashio, Kanehisa Kota, Matsumoto Sayaka, Okada Yoko, Kitazawa Riko, Kunieda Takeharu

机构信息

Department of Neurosurgery, Ehime University School of Medicine, Toon, Japan.

Department of Hematology, Clinical Immunology and Infectious Diseases, Ehime University School of Medicine, Toon, Japan.

出版信息

Surg Neurol Int. 2024 Feb 9;15:41. doi: 10.25259/SNI_8_2024. eCollection 2024.

Abstract

BACKGROUND

Primary intramedullary spinal cord lymphoma (PISCL) is an extremely rare condition. Early diagnosis is very difficult due to the nonspecific clinical and imaging findings. A biopsy is essential for a definitive diagnosis, but courage is required to perform the surgery. Here, we present a case of PISCL and suggest useful indicators for accurate diagnosis of this pathological entity.

CASE DESCRIPTION

A 70-year-old woman presented with subacute bilateral lower-limb paralysis, disturbance of warm and pain sensations, and vesicorectal disturbance. Magnetic resonance imaging showed a contrast-enhanced mass from C7 to Th2 and large, edematous lesions from the upper cervical to lower thoracic spinal cord. Elevated uptake of F-fluoro-2-deoxy-D-glucose (FDG) was identified in the enhanced regions on FDG-positron emission tomography (PET). Cerebrospinal fluid (CSF) analysis revealed highly elevated levels of β2-microglobulin (β2-MG). Steroid pulse therapy and therapeutic plasma exchange were performed for suspected myelitis, but symptoms did not improve. Spinal cord biopsy was, therefore, performed for treatment-resistant myelopathy. Histopathological examination revealed diffuse large B-cell lymphoma, which was diagnosed as PISCL because systemic examination showed no other findings suggestive of malignant lymphoma.

CONCLUSION

In cases with poor response to treatment and a progressive course, PISCL should be considered, and spinal cord biopsy should be performed if PET shows increased F-FDG uptake and β2-MG is elevated in CSF.

摘要

背景

原发性脊髓内淋巴瘤(PISCL)是一种极为罕见的疾病。由于临床和影像学表现不具有特异性,早期诊断非常困难。活检对于明确诊断至关重要,但进行手术需要勇气。在此,我们报告一例PISCL病例,并提出有助于准确诊断这一病理实体的有用指标。

病例描述

一名70岁女性,表现为亚急性双侧下肢瘫痪、温痛觉障碍及膀胱直肠功能障碍。磁共振成像显示C7至T2水平有一强化肿块,颈上段至胸下段脊髓有大片水肿性病变。氟代脱氧葡萄糖(FDG)正电子发射断层扫描(PET)显示强化区域FDG摄取增加。脑脊液(CSF)分析显示β2微球蛋白(β2-MG)水平显著升高。因怀疑为脊髓炎进行了类固醇冲击治疗和治疗性血浆置换,但症状未改善。因此,为治疗抵抗性脊髓病进行了脊髓活检。组织病理学检查显示为弥漫性大B细胞淋巴瘤,由于全身检查未发现其他提示恶性淋巴瘤的表现,故诊断为PISCL。

结论

对于治疗反应不佳且病情进展的病例,应考虑PISCL,若PET显示F-FDG摄取增加且CSF中β2-MG升高,则应进行脊髓活检。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5579/10927179/f706e19a02b5/SNI-15-41-g001.jpg

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