Chen Hai, Dong Huiqing
Department of Neurology, Xuanwu Hospital of Capital Medical University, Beijing, People`s Republic of China.
Neurosciences (Riyadh). 2015 Oct;20(4):380-4. doi: 10.17712/nsj.2015.4.20150125.
Primary central nervous system lymphoma (PCNSL) is reported to have increased in the last decades. Early diagnosis is crucial for proper management of this tumor. We report a case of a 48-year-old man who was initially diagnosed with multiple sclerosis. Magnetic resonance imaging of the brain revealed multiple lesions with hyper-signals in the bilateral basal ganglia and brain stem in T2-weighted image and non-enhancement, while positron emission tomography showed a low uptake of 18F-fluorodeoxyglucose in the affected brain, indicative of demyelination. However, this individual was correctly diagnosed with PCNSL after biopsy and further histological analysis. Primary central nervous system lymphoma must be considered even when nonenhancing, diffuse lesions are seen on MRI. A visible tumor on imaging is essential to ensure an early brain biopsy and histological diagnosis.
据报道,原发性中枢神经系统淋巴瘤(PCNSL)在过去几十年中有所增加。早期诊断对于该肿瘤的恰当管理至关重要。我们报告一例48岁男性病例,该患者最初被诊断为多发性硬化症。脑部磁共振成像显示,在T2加权图像上双侧基底神经节和脑干有多个高信号病变且无强化,而正电子发射断层扫描显示患侧大脑18F-氟脱氧葡萄糖摄取较低,提示脱髓鞘。然而,经活检及进一步组织学分析后,该个体被正确诊断为PCNSL。即使在MRI上看到无强化的弥漫性病变,也必须考虑原发性中枢神经系统淋巴瘤。影像学上可见的肿瘤对于确保早期脑活检和组织学诊断至关重要。