Rapid development of giant aneurysm at the base of the brain in an 8-year-old boy with perinatal HIV infection.

Acta histochemica. Supplementband Pub Date : 1992-01-01
C Lang, G Jacobi, W Kreuz, H Hacker, G Herrmann, H G Keul, E Thomas
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Abstract

An 8-year-old boy with perinatal HIV infection developed a large fusiform aneurysm in the circle of Willis two years prior to death which was confirmed by radiological studies. The postmortem examinations revealed a predominantly intimal, proliferative lesion, and partial destruction of the internal elastic lamina in the involved arteries. Within the intima hyperplasia of fibroblasts and smooth muscle cells was observed. No inflammatory alterations, no granulomas and no multinucleated giant cells could be noted in the vascular walls and in the cerebral parenchyma. A small ischemic infarct was present in the left thalamus. Cerebellum, brainstem and medulla showed multiple areas of progressive multifocal leukoencephalopathy (PML). Immunohistochemistry with anti-gp41, a monoclonal antibody against HIV envelope did not exhibit any positive results. These findings implicate that the vascular lesion might be attributed to primary infection of the brain by HIV which led to a defect of elastic lamina and consecutive intimal hyperplasia. A second hypothesis could be based on the effect of extremely high dose AZT therapy avoiding inflammatory reaction after HIV infection.

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一名8岁围生期HIV感染男孩脑底部快速发展的巨大动脉瘤。
一名8岁的围产期艾滋病毒感染的男孩在死亡前两年在威利斯圈出现了一个大的梭状动脉瘤,放射学研究证实了这一点。尸检显示主要是内膜增生性病变,受累动脉内弹性板部分破坏。内膜内可见成纤维细胞和平滑肌细胞增生。血管壁及脑实质未见炎性改变,未见肉芽肿,未见多核巨细胞。左侧丘脑出现小的缺血性梗死。小脑、脑干和髓质表现为多区进行性多灶性脑白质病(PML)。抗HIV包膜单克隆抗体gp41免疫组化未见阳性结果。这些发现提示血管病变可能是由于HIV对大脑的原发性感染,导致弹性板缺陷和连续的内膜增生。第二种假设可能是基于极高剂量AZT治疗在HIV感染后避免炎症反应的效果。
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Immunocytochemical characterization of cytomegalovirus (CMV) infected giant cells in perinatal acquired human immunodeficiency virus (HIV) infection. Transglutaminase activity in human brain tumors. Is it still adequate to study the nervous system using methods of catalytic enzyme histochemistry? [Histochemical representation of acetylcholinesterase in Alzheimer's disease]. [Changes of microenvironment and tumor cell heterogeneity--consequences for bioptic diagnosis].
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