Hamilton R L, Martinez A J
University of Pittsburgh and Children's Hospital of Pittsburgh, Department of Pathology (Neuropathology), USA.
Brain Pathol. 1998 Jan;8(1):239-40.
A twenty-six year old, previously healthy nurse presented with new onset of seizures and was given a clinical diagnosis of herpes simplex encephalitis. After treatment with acyclovir there was incomplete resolution of the lesions by MRI scans and within a few months the patient's neurologic symptoms worsened, prompting a stereotactic biopsy. A diagnosis of progressive multifocal leukoencephalopathy (PML) was made using electron microscopy, and in situ hybridization studies. Subsequent to this biopsy, she was shown to be infected with human immunodeficiency virus (HIV) and had a CD4 T-cell count of 63. She had no known risk factors for HIV infections and had been tested as recently as eighteen months previously during her pregnancy. Neither the husband nor the child were positive for HIV. PML as a presenting sign of HIV infection is rare.
一名26岁、此前身体健康的护士出现新发癫痫发作,临床诊断为单纯疱疹性脑炎。接受阿昔洛韦治疗后,MRI扫描显示病灶未完全消退,几个月内患者的神经症状恶化,促使进行立体定向活检。通过电子显微镜检查和原位杂交研究确诊为进行性多灶性白质脑病(PML)。此次活检后,发现她感染了人类免疫缺陷病毒(HIV),CD4 T细胞计数为63。她没有已知的HIV感染风险因素,在怀孕前18个月内最近一次接受过检测。丈夫和孩子的HIV检测均为阴性。PML作为HIV感染的首发症状很罕见。