Central Nervous System Cryptococcal Infections in Non-HIV Infected Patients

被引:67
|
作者
Beardsley, Justin [1 ]
Sorrell, Tania C. [1 ,2 ]
Chen, Sharon C. -A. [1 ,3 ]
机构
[1] Univ Sydney, Marie Bashir Inst Infect Dis & Biosecur, Sydney, NSW 2145, Australia
[2] Westmead Inst Med Res, Sydney, NSW 2145, Australia
[3] Univ Sydney, Ctr Infect Dis & Microbiol Lab Serv, Inst Clin Pathol & Med Res, NSW Hlth Pathol,Westmead Hosp, Sydney, NSW 2145, Australia
关键词
Cryptococcosis; Cryptococcus neoformans; Cryptococcus gattii; central nervous system; meningo-encephalitis; cerebral infection; HIV-negative patients; epidemiology; antifungal therapy; ORGAN TRANSPLANT RECIPIENTS; IMMUNE RECONSTITUTION SYNDROME; INVASIVE FUNGAL-INFECTIONS; SOLID-ORGAN; CLINICAL-FEATURES; GATTII INFECTION; ANTIFUNGAL SUSCEPTIBILITY; DIABETES-MELLITUS; BRITISH-COLUMBIA; RISK-FACTORS;
D O I
10.3390/jof5030071
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
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.
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页数:23
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