K. Lemtouni, R. Essofi, Y. Bouktib, A. E. Hajjami, B. Boutakioute, M. Ouali, N. E. Idrissi
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引用次数: 0
摘要
累及胼胝体的原发性中枢神经系统淋巴瘤(PCNSL)非常罕见,诊断也很困难。我们报告了一名患有认知障碍和人格改变的 63 岁女性。磁共振成像(MRI)显示胼胝体有高张力病变,活检证实为弥漫大 B 细胞淋巴瘤(DLBCL)。该病例强调了在胼胝体病变的鉴别诊断中考虑 PCNSL 的重要性,并强调尽管预后不佳,但仍有必要进行及时、积极的治疗。
Corpus Callosum Lymphoma in an Immunocompetent Patient: A Case Report
Primary central nervous system lymphoma (PCNSL) involving the corpus callosum is rare and diagnostically challenging. We report a 63-year-old female with cognitive impairment, and personality changes. MRI showed a hyperintense lesion in the corpus callosum, and biopsy confirmed diffuse large B-cell lymphoma (DLBCL). This case highlights the importance of considering PCNSL in differential diagnoses of corpus callosum lesions and underscores the necessity for prompt, aggressive treatment despite a guarded prognosis.