Viali S, Hutchinson D O, Hawkins T E, Croxson M C, Thomas M, Allen J P, Thomas S M, Powell K H
Department of Neurology, Auckland Hospital, New Zealand.
Muscle Nerve. 2000 Aug;23(8):1295-300. doi: 10.1002/1097-4598(200008)23:8<1295::aid-mus24>3.0.co;2-e.
A 53-year-old man developed progressive sensory disturbance and weakness in the legs, sphincter disturbance, back pain, systemic symptoms, and pancytopenia. Electrophysiological tests indicated a widespread lumbosacral polyradiculopathy. Spinal magnetic resonance imaging and routine cerebrospinal fluid analysis showed minor nonspecific abnormalities. Bone marrow and liver biopsies showed hemophagocytosis; and polymerase chain reaction of cerebrospinal fluid, bone marrow, and serum suggested active infection with human herpesvirus-6. Autopsy revealed that his neurological symptoms resulted from intravascular lymphomatosis (angiotropic large cell lymphoma), a rare variant of lymphoma with predilection for the nervous system.
一名53岁男性出现进行性感觉障碍、腿部无力、括约肌功能障碍、背痛、全身症状和全血细胞减少。电生理检查显示广泛的腰骶部多发性神经根病。脊髓磁共振成像和常规脑脊液分析显示轻微的非特异性异常。骨髓和肝脏活检显示噬血细胞现象;脑脊液、骨髓和血清的聚合酶链反应提示人类疱疹病毒6型活跃感染。尸检显示,他的神经症状是由血管内淋巴瘤(嗜血管大细胞淋巴瘤)引起的,这是一种罕见的淋巴瘤变异型,易侵犯神经系统。