Department of Hematology and Oncology, Charité Universitätsmedizin, Campus Benjamin Franklin, Hindenburgdamm 30, 12200 Berlin, Germany.
J Neurooncol. 2011 Mar;102(1):163-6. doi: 10.1007/s11060-010-0287-5. Epub 2010 Jul 3.
Primary CNS lymphoma (PCNSL) and its variant primary intraocular lymphoma (PIOL) are rare forms of extranodal non-Hodgkin's lymphoma confined to the CNS including the retina and the optical nerve; histologically, most cases are diffuse large B cell lymphomas. PCNSL in immunocompetent patients display typical radiological features on MRI, i.e. intensely and homogeneously enhancing lesions with moderate edema. Here, we report a 52-year-old male with a history of a PIOL and two consecutive intracerebral relapses who presented with dysarthria, dysphagia, and gait ataxia. Gadolinium-enhanced T1 scans were unremarkable but multiple lesions with restricted water diffusivity were seen on diffusion-weighted imaging. Relapse of his PCNSL was secured histologically only on autopsy. The possible etiology of the diffusion-restricted lesions is discussed.
原发性中枢神经系统淋巴瘤(PCNSL)及其变体原发性眼内淋巴瘤(PIOL)是罕见的结外非霍奇金淋巴瘤形式,局限于 CNS 包括视网膜和视神经;组织学上,大多数病例为弥漫性大 B 细胞淋巴瘤。免疫功能正常的 PCNSL 患者在 MRI 上显示典型的影像学特征,即强烈且均匀增强的病变伴中度水肿。在这里,我们报告了一名 52 岁男性,他患有 PIOL 和两次连续的颅内复发,表现为构音障碍、吞咽困难和步态共济失调。钆增强 T1 扫描未见异常,但在弥散加权成像上可见多个限制水弥散的病变。他的 PCNSL 的复发仅在尸检时得到组织学证实。讨论了弥散受限病变的可能病因。