Pandit Lekha, Chickabasaviah Yasha, Raghothaman Ananthan, Mustafa Sharik, Vasudevan Arvind
Department of Neurosciences, KS Hegde Medical Academy, Mangalore, Karnataka, India.
J Neurol Sci. 2010 Jun 15;293(1-2):122-4. doi: 10.1016/j.jns.2010.02.023. Epub 2010 Mar 20.
Lymphomatosis cerebri is a rare variant of primary central nervous system lymphoma. Clinically it presents usually as rapidly progressive dementia and is accompanied by extensive white matter changes in magnetic resonance imaging (MRI).
A 49-year-old immuno-competent male who complained of dull diffuse headache, rapidly deteriorated in higher functions over a 6 month period. On examination he was globally declined in cognitive functions and had papilledema. MRI showed extensive white matter lesions. He became temporarily alert, and attentive after a course of parenteral steroids. However within three weeks he relapsed and a wedge biopsy of the brain revealed histopathology consistent with lymphomatosis cerebri.
The differential diagnosis of diffuse white matter diseases is constantly expanding. In the background of a rapidly progressing subcortical dementia and extensive white matter disease, neoplastic disorders of the brain especially lymphomatosis cerebri should be considered. Early tissue diagnosis is important for specific treatment and interventions.
脑淋巴瘤病是原发性中枢神经系统淋巴瘤的一种罕见变体。临床上通常表现为快速进展性痴呆,并伴有磁共振成像(MRI)上广泛的白质改变。
一名49岁免疫功能正常的男性,主诉弥漫性钝痛,在6个月内高级功能迅速恶化。检查发现他的认知功能全面下降且有视乳头水肿。MRI显示广泛的白质病变。经静脉注射类固醇治疗一个疗程后,他暂时变得警觉和专注。然而,三周内他复发了,脑部楔形活检的组织病理学结果与脑淋巴瘤病一致。
弥漫性白质疾病的鉴别诊断范围在不断扩大。在快速进展的皮质下痴呆和广泛白质疾病的背景下,应考虑脑部肿瘤性疾病,尤其是脑淋巴瘤病。早期组织诊断对于特定治疗和干预很重要。