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dc.contributor.authorChowdhary, A.
dc.contributor.authorMeis, J. F.
dc.contributor.authorGuarro, J.
dc.contributor.authorde Hoog, G. S.
dc.contributor.authorKathuria, S.
dc.contributor.authorArendrup, M. C.
dc.contributor.authorArikan-Akdagli, S.
dc.contributor.authorAkova, M.
dc.contributor.authorBoekhout, T.
dc.contributor.authorCaira, M.
dc.contributor.authorGuinea, J.
dc.contributor.authorChakrabarti, A.
dc.contributor.authorDannaoui, E.
dc.contributor.authorvan Diepeningen, A.
dc.contributor.authorFreiberger, T.
dc.contributor.authorGroll, A. H.
dc.contributor.authorHope, W. W.
dc.contributor.authorJohnson, E.
dc.contributor.authorLackner, M.
dc.contributor.authorLagrou, K.
dc.contributor.authorLanternier, F.
dc.contributor.authorLass-Floerl, C.
dc.contributor.authorLortholary, O.
dc.contributor.authorMeletiadis, J.
dc.contributor.authorMunoz, P.
dc.contributor.authorPagano, L.
dc.contributor.authorPetrikkos, G.
dc.contributor.authorRichardson, M. D.
dc.contributor.authorRoilides, E.
dc.contributor.authorSkiada, A.
dc.contributor.authorTortorano, A. M.
dc.contributor.authorUllmann, A. J.
dc.contributor.authorVerweij, P. E.
dc.contributor.authorCornely, O. A.
dc.contributor.authorCuenca-Estrella, M.
dc.date.accessioned2019-12-12T06:24:31Z
dc.date.available2019-12-12T06:24:31Z
dc.date.issued2014
dc.identifier.issn1198-743X
dc.identifier.urihttps://doi.org/10.1111/1469-0691.12515
dc.identifier.urihttp://hdl.handle.net/11655/16172
dc.description.abstractThe aetiological agents of many invasive fungal infections are saprobes and opportunistic pathogens. Some of these fungi are darkly pigmented due to melanin production and traditionally have been named dematiaceous'. The melanized fungi cause a wide array of clinical syndromes ranging from superficial to deep-seated infections. Diagnosis relies on histopathological examination of clinical specimens and on examination of cultures. Sequencing is recommended for accurate species identification, especially for unusual or newly described pathogens. In cases of mycetoma and chromoblastomycosis, pathognomonic histological findings are useful and the Fontana-Masson stain, specific for melanin, usually confirms the diagnosis. There are no standardized therapies but voriconazole, posaconazole and itraconazole demonstrate the most consistent in vitro activity against this group of fungi. Oral itraconazole has been considered the drug of choice, given the extensive clinical experience with this drug. However, voriconazole may presumably be superior for central nervous system infections because of its ability to achieve good levels in the cerebrospinal fluid. Posaconazole is a well-tolerated alternative drug, backed by less clinical experience but with excellent salvage treatment results after failure of other antifungals. Amphotericin B has been useful as alternative therapy in some cases. Combination antifungal therapy is recommended for cerebral abscesses when surgery is not possible and for disseminated infections in immunocompromised patients.
dc.language.isoen
dc.publisherElsevier Sci Ltd
dc.relation.isversionof10.1111/1469-0691.12515
dc.rightsinfo:eu-repo/semantics/openAccess
dc.subjectInfectious Diseases
dc.subjectMicrobiology
dc.titleEscmid And Ecmm Joint Clinical Guidelines For The Diagnosis And Management Of Systemic Phaeohyphomycosis: Diseases Caused By Black Fungi
dc.typeinfo:eu-repo/semantics/article
dc.typeinfo:eu-repo/semantics/publishedVersion
dc.relation.journalClinical Microbiology And Infection
dc.contributor.departmentTıbbi Mikrobiyoloji
dc.identifier.volume20
dc.identifier.startpage47
dc.identifier.endpage75
dc.description.indexWoS
dc.description.indexScopus


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