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自发性肉芽肿性阿米巴脑炎:来自泰国的4例报告。

Spontaneous granulomatous amebic encephalitis: report of four cases from Thailand.

作者信息

Sangruchi T, Martinez A J, Visvesvara G S

机构信息

Department of Pathology, Siriraj Hospital Mahidol University, Bangkok, Thailand.

出版信息

Southeast Asian J Trop Med Public Health. 1994 Jun;25(2):309-13.

PMID:7855646
Abstract

Granulomatous amebic encephalitis (GAE), or meningoencephalitis caused by Acanthamoeba sp and leptomyxid amebae are uncommon CNS infections that usually occur in an immunocompromised host. From 1990 to 1992, 4 patients with GAE were treated at Siriraj Hospital, Bangkok. One case was diagnosed antemortem, from a brain biopsy. The other three cases were diagnosed as GAE postmortem. Pathological findings included acute and subacute granulomatous inflammation with extensive cerebral necrosis, angiitis, fibrinoid necrosis and fibrin thrombi. One patient had a chronic skin ulcer in which free-living amebic trophozoites were found. No visceral involvement was observed. All patients developed "spontaneous" GAE, but we suspect an undiagnosed abnormality in cell mediated immunity or a deficient humoral immune response.

摘要

肉芽肿性阿米巴脑炎(GAE),即由棘阿米巴属和瘦黏菌属阿米巴引起的脑膜脑炎,是一种罕见的中枢神经系统感染,通常发生在免疫功能低下的宿主中。1990年至1992年期间,曼谷诗里拉吉医院收治了4例GAE患者。其中1例通过脑活检在生前确诊。另外3例在死后被诊断为GAE。病理检查结果包括急性和亚急性肉芽肿性炎症,并伴有广泛的脑坏死、血管炎、纤维蛋白样坏死和纤维蛋白血栓形成。1例患者有慢性皮肤溃疡,在溃疡中发现了自由生活的阿米巴滋养体。未观察到内脏受累情况。所有患者均发生了“自发性”GAE,但我们怀疑其细胞介导免疫存在未被诊断出的异常或体液免疫反应不足。

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