Martínez A J, Sotelo-Avila C, Alcalá H, Willaert E
Acta Neuropathol. 1980;49(1):7-12. doi: 10.1007/BF00692213.
Primary amebic meningoencephalitis and granulomatous amebic encephalitis are well recognized clinicopathological entities caused by free-living amebas. Associated arteritis and "mycotic aneurysms" with infiltration of intracranial arteries by lymphocytes, amebic trophozoites and cysts have not been previously reported. A 26-month-old girl had a 3-week history of encephalitis, characterized, initially, by vomiting and low-grade fever. Subsequently, she developed ataxia, generalized weakness, lethargy, and esotropia. The first CSF showed 490 RBC/microliters, 705 WBC/microliters with 90% mononuclears. Her pupils reacted briskly to light. Moderate nuchal rigidity, nystagmus, fixed downward gaze, anisocoria, bilateral 6th nerve palsy, left arm monoparesis and left Babinski were present. CAT scan revealed slight symmetrical dilatation of anterior horns of lateral ventricles and an area of abnormal enhancement above the 3rd ventricle. She died 14 days after admission, 5 weeks after onset of symptoms. The brain showed focal necrotizing encephalopathy, involving thalami, cerebellum, brain stem, and cervical and upper thoracic spinal cord. Numerous free-living amebic trophozoites and cysts were present within a chronic granulomatous encephalitis. There were trombosis of basilar, posterior cerebral, and vertebral arteries with profuse chronic panarteritis, fibrinoid necrosis, and mycotic aneurysms.
原发性阿米巴脑膜脑炎和肉芽肿性阿米巴脑炎是由自由生活阿米巴引起的公认临床病理实体。此前尚未报道过伴有动脉炎和“霉菌性动脉瘤”以及淋巴细胞、阿米巴滋养体和囊肿浸润颅内动脉的情况。一名26个月大的女孩有3周的脑炎病史,最初表现为呕吐和低热。随后,她出现共济失调、全身无力、嗜睡和内斜视。首次脑脊液检查显示每微升有490个红细胞、705个白细胞,其中90%为单核细胞。她的瞳孔对光反应灵敏。存在中度颈项强直、眼球震颤、固定向下凝视、瞳孔不等大、双侧第六脑神经麻痹、左臂单瘫和左侧巴宾斯基征。计算机断层扫描显示侧脑室前角轻度对称性扩张以及第三脑室上方有异常强化区域。她在入院14天后、症状出现5周后死亡。脑部显示局灶性坏死性脑病,累及丘脑、小脑、脑干以及颈段和上胸段脊髓。在慢性肉芽肿性脑炎内可见大量自由生活阿米巴滋养体和囊肿。基底动脉、大脑后动脉和椎动脉有血栓形成,伴有大量慢性全动脉炎、纤维蛋白样坏死和霉菌性动脉瘤。