Hudson H L, Hinton D R, Friedman D I, Apuzzo M, Chandrasoma P, Garbut M, Feldon S E
Department of Ophthalmology, University of Southern California, Los Angeles, Riverside, USA.
J Neuroophthalmol. 1996 Sep;16(3):208-11.
A 42-year-old immune-competent woman with orbital pseudotumor and presumed intracranial extension into the temporal lobe responded well clinically and radiologically to high-doses of corticosteroids. Five months later, she developed worsening headaches and recurrence of the temporal lobe lesion. Biopsy revealed a central nervous system (CNS) lymphoma with severe reactive gliosis abutting an area of subarachnoid lymphocytic infiltrate.
一名42岁免疫功能正常的女性,患有眼眶假瘤,推测颅内已蔓延至颞叶,对大剂量皮质类固醇激素治疗在临床和影像学上反应良好。五个月后,她出现头痛加重和颞叶病变复发。活检显示为中枢神经系统(CNS)淋巴瘤,伴有严重的反应性胶质增生,紧邻蛛网膜下腔淋巴细胞浸润区域。