Neuen-Jacob E, Figge C, Arendt G, Wendtland B, Jacob B, Wechsler W
Department of Neuropathology, Heinrich-Heine-University, Düsseldorf, Germany.
Int J Legal Med. 1993;105(6):339-50. doi: 10.1007/BF01222119.
The brains of 70 fatal cases with AIDS were studied by means of immunohistochemistry and in-situ hybridization in a consecutive autopsy series (1985-July 1992). In addition, the neuropathological changes were correlated with the neurological and neuroimaging findings. Opportunistic infections included toxoplasmosis (15 cases), cytomegalovirus (CMV)-encephalitis (6), progressive multifocal leucoencephalopathy (2) and fungal infections (3). Malignant lymphomas were found in 7 patients; 6 involved primarily the CNS, one was metastatic. In 14 cases the neuropathological changes were consistent with HIV encephalitis and HIV leucoencephalopathy. Non-specific lesions occurred in 31 cases. The clinical diagnosis in patients with opportunistic diseases (n = 27) diverged in 15 cases (55%) from the underlying pathology. Toxoplasma gondii, CMV and JC viruses were identified by immunohistochemistry and in-situ hybridization on serial paraffin sections. In addition, antibodies against lymphocyte subsets, tissue macrophages, the glial fibrillary acid protein (GFAP) and myelin basic protein were used to characterize the phenotype of cells and to highlight the degree of gliosis and demyelination. Our results show that the distribution and degree of morphological changes might be helpful for the differential diagnosis antemortem. Since neurological complications may represent the first or sole manifestation of AIDS and risk factors for AIDS are often not known, it should be taken into account that CNS manifestations of AIDS may contribute to a sudden and unexpected death or accident. Opportunistic diseases should be considered as a possible differential diagnosis in cases mimicking the clinical picture of apoplexia or dementia. Furthermore, CNS lesions may be detected postmortem in patients who were not known to suffer from Neuro-Aids during life, indicating that CNS involvement is more widespread than assumed.
通过免疫组织化学和原位杂交技术,对1985年至1992年7月间连续尸检的70例艾滋病死亡病例的大脑进行了研究。此外,将神经病理学变化与神经学和神经影像学检查结果进行了关联分析。机会性感染包括弓形虫病(15例)、巨细胞病毒(CMV)脑炎(6例)、进行性多灶性白质脑病(2例)和真菌感染(3例)。7例患者发现恶性淋巴瘤;6例主要累及中枢神经系统,1例为转移性。14例患者的神经病理学变化符合HIV脑炎和HIV白质脑病。31例出现非特异性病变。27例患有机会性疾病患者的临床诊断与潜在病理学诊断在15例(55%)中存在差异。通过对连续石蜡切片进行免疫组织化学和原位杂交,鉴定出弓形虫、CMV和JC病毒。此外,还使用了针对淋巴细胞亚群、组织巨噬细胞、胶质纤维酸性蛋白(GFAP)和髓鞘碱性蛋白的抗体来表征细胞表型,并突出胶质增生和脱髓鞘程度。我们的结果表明,形态学变化的分布和程度可能有助于生前鉴别诊断。由于神经系统并发症可能是艾滋病的首发或唯一表现,且艾滋病的危险因素往往未知,因此应考虑到艾滋病的中枢神经系统表现可能导致突然和意外的死亡或事故。在模拟中风或痴呆临床表现的病例中,应将机会性疾病视为可能的鉴别诊断。此外,生前未被诊断为神经艾滋病的患者在死后可能检测到中枢神经系统病变,这表明中枢神经系统受累比预期更为广泛。