Calamia K T, Miller A, Shuster E A, Perniciaro C, Menke D M
Department of Rheumatology, Mayo Clinic Jacksonville, Florida 32224, USA.
Adv Exp Med Biol. 1999;455:249-65.
The clinical, radiographic, and pathological findings in ten cases of intravascular lymphomatosis with central nervous system involvement seen at our institution over a 15-year period are presented. Nine patients presented with a subacute, progressive multifocal neurologic disorder. Most patients had fever, anemia, and elevation of the erythrocyte sedimentation rate. As the illness evolved, computerized tomography scanning and magnetic resonance imaging showed evidence of multifocal central nervous system disease. Angiography was nondiagnostic but suggested vasculitis in six cases. A response to empiric corticosteroid treatment was typical but usually transient. In six patients, the diagnosis was made antemortem by brain biopsy. The prognosis of patients was primarily dependent on early diagnosis and treatment, before massive central nervous system damage occurred. Treatment with chemotherapy, with or without radiotherapy, was associated with stabilization of the disease in three of five patients.
本文介绍了我院15年间收治的10例累及中枢神经系统的血管内淋巴瘤的临床、影像学和病理学表现。9例患者表现为亚急性、进行性多灶性神经系统疾病。大多数患者有发热、贫血和红细胞沉降率升高。随着病情进展,计算机断层扫描和磁共振成像显示有多灶性中枢神经系统疾病的证据。血管造影无诊断价值,但6例提示血管炎。经验性使用皮质类固醇治疗通常有效,但多为短暂缓解。6例患者在生前通过脑活检确诊。患者的预后主要取决于在中枢神经系统发生严重损害之前的早期诊断和治疗。5例患者中有3例接受化疗(联合或不联合放疗)后病情稳定。