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首页> 外文期刊>Journal of Fungi >Central Nervous System Cryptococcal Infections in Non-HIV Infected Patients
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Central Nervous System Cryptococcal Infections in Non-HIV Infected Patients

机译:非HIV感染患者的中枢神经系统隐球菌感染

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摘要

Central nervous system (CNS) cryptococcosis in non-HIV infected patients affects solid organ transplant (SOT) recipients, patients with malignancy, rheumatic disorders, other immunosuppressive conditions and immunocompetent hosts. More recently described risks include the use of newer biologicals and recreational intravenous drug use. Disease is caused by Cryptococcus neoformans and Cryptococcus gattii species complex; C. gattii is endemic in several geographic regions and has caused outbreaks in North America. Major virulence determinants are the polysaccharide capsule, melanin and several ‘invasins’. Cryptococcal plb1, laccase and urease are essential for dissemination from lung to CNS and crossing the blood–brain barrier. Meningo-encephalitis is common but intracerebral infection or hydrocephalus also occur, and are relatively frequent in C. gattii infection. Complications include neurologic deficits, raised intracranial pressure (ICP) and disseminated disease. Diagnosis relies on culture, phenotypic identification methods, and cryptococcal antigen detection. Molecular methods can assist. Preferred induction antifungal therapy is a lipid amphotericin B formulation (amphotericin B deoxycholate may be used in non-transplant patients) plus 5-flucytosine for 2–6 weeks depending on host type followed by consolidation/maintenance therapy with fluconazole for 12 months or longer. Control of raised ICP is essential. Clinicians should be vigilant for immune reconstitution inflammatory syndrome.
机译:非HIV感染患者的中枢神经系统(CNS)隐球菌感染会影响实体器官移植(SOT)受体,恶性肿瘤,风湿性疾病,其他免疫抑制疾病和具有免疫能力的宿主。最近描述的风险包括使用更新的生物制剂和休闲性静脉内吸毒。疾病是由新型隐球菌和加蒂隐球菌物种复合体引起的;加迪梭菌在几个地理区域内都很流行,并在北美引起了暴发。主要的毒性决定因素是多糖胶囊,黑色素和几种“入侵素”。隐球菌plb1,漆酶和脲酶对于从肺到中枢神经系统的传播以及穿越血脑屏障至关重要。脑膜脑炎很常见,但脑内感染或脑积水也发生,在加蒂氏梭菌感染中相对频繁。并发症包括神经功能缺损,颅内压升高(ICP)和播散性疾病。诊断依赖于培养,表型鉴定方法和隐球菌抗原检测。分子方法可以提供帮助。优选的诱导抗真菌治疗是脂质两性霉素B制剂(非移植患者可使用两性霉素B脱氧胆酸盐)加5-氟胞嘧啶2-6周,具体取决于宿主类型,然后用氟康唑进行巩固/维持治疗12个月或更长时间。控制升高的ICP是必不可少的。临床医生应对免疫重建炎症综合征保持警惕。

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