Primary dural Lymphoma: A case report

IF 0.4 Q4 CLINICAL NEUROLOGY
IBRAHIM Al-hassana Idriss , Hounkpatin Stachys , Mehome Wilfried , Setcheou Alexis , Sieleche Christian , Tankari Aboubacar , Sawa Brice , Jermidi Cynthia , Lethongsavarn Vincent , Helias Phillipe , Assoumane Ibrahim , Kelani Aminath , Rabhi Mohammed , Sanoussi Samuila , Do Laurent
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引用次数: 0

Abstract

Backgroung

Primary dural lymphoma is a very rare pathology arising from the dura mater. its clinical and radiological presentation is often similar to a meningioma. Treatment typically involves surgery followed by adjuvant radiotherapy/chemotherapy. Fewer than twenty cases have been described in the literature.

Case presentation

A 73-year-old woman with a medical history of hypertension, type 2 diabetes, and dyslipidemia presented with progressive right hemiparesis. Following diagnostic evaluation, a left fronto-temporal meningioma was initially diagnosed. Complete macroscopic excision was made and the immunohistochemical showed a follicular B lymphoma according. the patient had radiotherapy and chemotherapy sessions. Follow-up at 18 months was unremarkable.

Conclusion

Primary dural lymphoma is an exceptionally rare pathology, often mimicking the radiological appearance of a meningioma. The management relies on complete tumor excision, along with a combination of radiotherapy and chemotherapy. When administered appropriately, this treatment approach offers a favorable prognosis for patients.

原发性硬脑膜淋巴瘤:病例报告
背景介绍原发性硬脑膜淋巴瘤是一种非常罕见的病变,发生于硬脑膜,其临床和放射学表现通常与脑膜瘤相似。治疗通常包括手术和辅助放疗/化疗。文献中描述的病例不到 20 例。病例介绍一位 73 岁的妇女,有高血压、2 型糖尿病和血脂异常病史,并伴有进行性右侧偏瘫。经过诊断评估,初步诊断为左侧额颞部脑膜瘤。患者接受了放疗和化疗。结论原发性硬脑膜淋巴瘤是一种非常罕见的病理现象,通常会模仿脑膜瘤的放射学表现。治疗方法主要是彻底切除肿瘤,同时结合放疗和化疗。如果用药得当,这种治疗方法可为患者带来良好的预后。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
1.00
自引率
0.00%
发文量
236
审稿时长
15 weeks
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