一例罕见的新发传染病——曼氏巴通体阿米巴脑炎尸检病例,并简要回顾日本报告的病例
An autopsy case of Balamuthia mandrillaris amoebic encephalitis, a rare emerging infectious disease, with a brief review of the cases reported in Japan.
作者信息
Itoh Kyoko, Yagita Kenji, Nozaki Tomoyoshi, Katano Harutaka, Hasegawa Hideki, Matsuo Koushun, Hosokawa Youhei, Tando So, Fushiki Shinji
机构信息
Department of Pathology & Applied Neurobiology, Graduate School of Medical Science, Kyoto Prefectural University of Medicine, Kyoto, Japan.
出版信息
Neuropathology. 2015 Feb;35(1):64-9. doi: 10.1111/neup.12151. Epub 2014 Sep 3.
Balamuthia mandrillaris is an amoeba found in fresh water and soil that causes granulomatous amoebic encephalitis. We report herein an autopsy case of B. mandrillaris amoebic encephalitis, which was definitely diagnosed by PCR. An 81-year-old man, who had Sjögren's syndrome, manifested drowsiness 2 months before his death with progressive deterioration. Neuroimaging demonstrated foci of T2- and fluid-attenuated inversion recovery high and T1 low-intensity with irregular post-contrast ring enhancement in the cerebral hemisphere, thalamus and midbrain. Pathologically, multiple hemorrhagic and necrotic lesions were found in the cerebrum, thalamus, midbrain, pons, medulla and cerebellum, which were characterized by liquefactive necrosis, marked edema, hemorrhage and necrotizing vasculitis associated with the perivascular accumulation of amoebic trophozoites, a few cysts, and the infiltration of numerous neutrophils and microglia/macrophages. The trophozoites were ovoid or round, 10-60 μm in diameter, and they showed foamy cytoplasm and a round nucleus with small karyosome in the center. The PCR and immunohistochemistry from paraffin-embedded brain specimens revealed angioinvasive encephalitis due to B. mandrillaris. Human cases of B. mandrillaris brain infection are rare in Japan, with only a few brief reports in the literature.
曼氏巴通体是一种存在于淡水和土壤中的变形虫,可引起肉芽肿性阿米巴脑炎。我们在此报告一例经聚合酶链反应(PCR)明确诊断的曼氏巴通体阿米巴脑炎尸检病例。一名81岁患有干燥综合征的男性,在死亡前2个月出现嗜睡,并进行性恶化。神经影像学检查显示大脑半球、丘脑和中脑有T2加权像及液体衰减反转恢复序列高信号、T1加权像低信号灶,增强扫描后有不规则环形强化。病理检查发现,大脑、丘脑、中脑、脑桥、延髓和小脑有多个出血性和坏死性病变,其特征为液化性坏死、明显水肿、出血和坏死性血管炎,伴有阿米巴滋养体在血管周围聚集、少量包囊,以及大量中性粒细胞和小胶质细胞/巨噬细胞浸润。滋养体呈卵圆形或圆形,直径10 - 60μm,细胞质呈泡沫状,细胞核圆形,中央有小核仁。石蜡包埋脑标本的PCR和免疫组织化学检查显示为曼氏巴通体引起的血管侵袭性脑炎。在日本,人类感染曼氏巴通体脑部的病例罕见,文献中仅有少数简短报道。