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动脉炎和致命性蛛网膜下腔出血并发隐匿性念珠菌性脑膜炎:小儿获得性免疫缺陷综合征的不寻常表现。

Arteritis and fatal subarachnoid hemorrhage complicating occult Candida meningitis: unusual presentation in pediatric acquired immunodeficiency syndrome.

作者信息

Rabah R, Kupsky W J, Haas J E

机构信息

Department of Pathology and Laboratory Medicine, Children's Hospital of Michigan, Detroit 48201, USA.

出版信息

Arch Pathol Lab Med. 1998 Nov;122(11):1030-3.

PMID:9822135
Abstract

We report the case of an 11-month-old child with acquired immunodeficiency syndrome, who despite treatment for systemic candidiasis developed undetected Candida meningitis. This uncommon manifestation of candidiasis was accompanied by basilar granulomatous inflammation and fibrosis of meninges with arteritis, vascular invasion by fungi, and terminal subarachold hemorrhage. To our knowledge, this constellation of findings has not been reported previously in pediatric acquired immunodeficiency syndrome.

摘要

我们报告了一例11个月大的获得性免疫缺陷综合征患儿,尽管接受了系统性念珠菌病治疗,但仍发生了未被检测出的念珠菌性脑膜炎。这种念珠菌病的罕见表现伴有基底膜肉芽肿性炎症和脑膜纤维化,并伴有动脉炎、真菌血管侵袭和终末期蛛网膜下腔出血。据我们所知,这种一系列的表现此前在儿童获得性免疫缺陷综合征中尚未有过报道。

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Refractory candidal meningitis in an immunocompromised patient cured by caspofungin.卡泊芬净治愈免疫功能低下患者的难治性念珠菌性脑膜炎。
J Clin Microbiol. 2004 Dec;42(12):5950-3. doi: 10.1128/JCM.42.12.5950-5953.2004.