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[原发性硬脑膜淋巴瘤:两例报告并文献复习]

[Primary dural lymphoma: a report of two cases with review of the literature].

作者信息

Benouaich A, Delord J-P, Danjou M, Richaud J, Urocoste E, Soum F, Aziza R, Roche H

机构信息

Département d'Oncologie Médicale, Institut Claudius Regaud, Toulouse.

出版信息

Rev Neurol (Paris). 2003 Jul;159(6-7 Pt 1):652-8.

Abstract

Primary lymphoma arising in dura is exceedingly rare. We report the clinicopathologic findings of two patients with primary B-cell lymphoma of dura. Both were female, 38 and 45 years old. Prior to biopsy they were felt to have meningioma on preoperative magnetic resonance imagery. Histologically, tumors were classified as MALT-type lymphoma. Literature describe only 14 reports of similar entity. Primary lymphomas arising in dura appear to have a more favourable clinical course compared to PCNSL and may require a less aggressive treatment.

摘要

起源于硬脑膜的原发性淋巴瘤极为罕见。我们报告了两名硬脑膜原发性B细胞淋巴瘤患者的临床病理特征。两名患者均为女性,年龄分别为38岁和45岁。活检前,术前磁共振成像显示她们被认为患有脑膜瘤。组织学上,肿瘤被分类为黏膜相关淋巴组织型淋巴瘤。文献中仅描述了14例类似病例的报告。与原发性中枢神经系统淋巴瘤相比,起源于硬脑膜的原发性淋巴瘤似乎具有更有利的临床病程,可能需要的治疗手段也不那么激进。

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