Central Nervous System Cryptococcal Infections in Non-HIV Infected Patients

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 an...

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Main Authors: Justin Beardsley, Tania C. Sorrell, Sharon C.-A. Chen
Format: Article
Language:English
Published: MDPI AG 2019-08-01
Series:Journal of Fungi
Subjects:
Online Access:https://www.mdpi.com/2309-608X/5/3/71
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spelling doaj-c6028a2d060c498aafc90b8b75edaf592020-11-25T01:57:17ZengMDPI AGJournal of Fungi2309-608X2019-08-01537110.3390/jof5030071jof5030071Central Nervous System Cryptococcal Infections in Non-HIV Infected PatientsJustin Beardsley0Tania C. Sorrell1Sharon C.-A. Chen2Marie Bashir Institute for Infectious Diseases and Biosecurity, The University of Sydney, Sydney 2145, AustraliaMarie Bashir Institute for Infectious Diseases and Biosecurity, The University of Sydney, Sydney 2145, AustraliaCentre for Infectious Diseases and Microbiology Laboratory Services, Institute of Clinical Pathology and Medical Research, NSW Health Pathology, Westmead Hospital and the Marie Bashir Institute for Infectious Diseases and Biosecurity, The University of Sydney, Sydney 2145, AustraliaCentral 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 <i>Cryptococcus neoformans</i> and <i>Cryptococcus gattii</i> species complex; <i>C. gattii</i> 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 <i>C. gattii</i> 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.https://www.mdpi.com/2309-608X/5/3/71Cryptococcosis<i>Cryptococcus neoformans</i><i>Cryptococcus gattii</i>central nervous systemmeningo-encephalitiscerebral infectionHIV-negative patientsepidemiologyantifungal therapy
collection DOAJ
language English
format Article
sources DOAJ
author Justin Beardsley
Tania C. Sorrell
Sharon C.-A. Chen
spellingShingle Justin Beardsley
Tania C. Sorrell
Sharon C.-A. Chen
Central Nervous System Cryptococcal Infections in Non-HIV Infected Patients
Journal of Fungi
Cryptococcosis
<i>Cryptococcus neoformans</i>
<i>Cryptococcus gattii</i>
central nervous system
meningo-encephalitis
cerebral infection
HIV-negative patients
epidemiology
antifungal therapy
author_facet Justin Beardsley
Tania C. Sorrell
Sharon C.-A. Chen
author_sort Justin Beardsley
title Central Nervous System Cryptococcal Infections in Non-HIV Infected Patients
title_short Central Nervous System Cryptococcal Infections in Non-HIV Infected Patients
title_full Central Nervous System Cryptococcal Infections in Non-HIV Infected Patients
title_fullStr Central Nervous System Cryptococcal Infections in Non-HIV Infected Patients
title_full_unstemmed Central Nervous System Cryptococcal Infections in Non-HIV Infected Patients
title_sort central nervous system cryptococcal infections in non-hiv infected patients
publisher MDPI AG
series Journal of Fungi
issn 2309-608X
publishDate 2019-08-01
description 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 <i>Cryptococcus neoformans</i> and <i>Cryptococcus gattii</i> species complex; <i>C. gattii</i> 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 <i>C. gattii</i> 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.
topic Cryptococcosis
<i>Cryptococcus neoformans</i>
<i>Cryptococcus gattii</i>
central nervous system
meningo-encephalitis
cerebral infection
HIV-negative patients
epidemiology
antifungal therapy
url https://www.mdpi.com/2309-608X/5/3/71
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