Di Gregorio C, Rivasi F, Mongiardo N, De Rienzo B, Wallace S, Visvesvara G S
Institute of Pathological Anatomy, University of Modena, Italy.
Arch Pathol Lab Med. 1992 Dec;116(12):1363-5.
Several cases of Acanthamoeba encephalitis (ie, granulomatous amebic encephalitis) have been reported in patients with acquired immunodeficiency syndrome from the United States. To our knowledge, none so far has been reported from Europe, and this is the first case of amebic meningoencephalitis due to Acanthamoeba in a patient with acquired immunodeficiency syndrome from Italy. The patient was a 24-year-old, human immunodeficiency virus-positive heterosexual man with a 6-year history of intravenous drug use. He was admitted to the hospital because of severe headache, confusion, nuchal rigidity, jaundice, and ascites. He died 5 days later. At autopsy, the brain showed extensive hemorrhagic necrosis with numerous trophic and cyst forms of Acanthamoeba. The amebas were identified as Acanthamoeba divionensis by the indirect immunofluorescence test.
在美国,已报告了几例获得性免疫缺陷综合征患者发生棘阿米巴脑炎(即肉芽肿性阿米巴脑炎)的病例。据我们所知,欧洲迄今尚未有此类病例报告,而这是意大利首例获得性免疫缺陷综合征患者因棘阿米巴引起的阿米巴脑膜脑炎病例。该患者为一名24岁的人类免疫缺陷病毒阳性异性恋男性,有6年静脉吸毒史。他因严重头痛、意识模糊、颈项强直、黄疸和腹水入院。5天后死亡。尸检时,大脑显示广泛出血性坏死,有大量棘阿米巴的滋养体和包囊形式。通过间接免疫荧光试验将阿米巴鉴定为迪氏棘阿米巴。