Primary cutaneous cryptococcosis – History, concepts, clinical and therapeutic update

Bibliographic Details
Main Author: Marques, Sílvio Alencar [UNESP]
Publication Date: 2025
Other Authors: Camargo, Rosangela Maria Pires de [UNESP]
Format: Article
Language: eng
Source: Repositório Institucional da UNESP
Download full: http://dx.doi.org/10.1016/j.abd.2024.07.004
https://hdl.handle.net/11449/303439
Summary: Cryptococcosis is a disease caused by fungi of the genus Cryptococcus, with the species Cryptococcus neoformans and Cryptococcus gattii being recognized as pathogenic. Cutaneous cryptococcosis can be classified as “secondary”, developing from a previous systemic disease, or, on the contrary, “primary”, resulting from transcutaneous inoculation of the agent. It can also be classified as “disseminated cutaneous cryptococcosis”, when there is an associated systemic disease, or “localized”, when it is restricted to the skin. This article uses the term “primary cutaneous cryptococcosis” because it is the most widely used and already established in the literature. Historically, the first report of a possible case of primary cutaneous cryptococcosis (PCC) occurred in 1950 by Gancy WM and was published in the Archives of Dermatology and Syphilology. Subsequently, the rare and sporadic reports in the following decades were reviewed and reported in the 1985 publication by Baes & van Cutsen. However, the unequivocal acceptance of the existence of PCC as a distinct disease only occurred in 2003 with the publication by Neville S et al. of the French Cryptococcosis Study Group. The fundamental criterion established to consider it as PCC was the proven absence of systemic disease, whether pulmonary, in the CNS or other location at the time of diagnosis of the cutaneous condition, characterized by a single lesion and, mostly, in an exposed area. These and other clinical criteria, diagnostic confirmation, and therapeutic choice are discussed in detail in the full text.
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spelling Primary cutaneous cryptococcosis – History, concepts, clinical and therapeutic updateClinical medicineCryptococcosisCryptococcosis/diagnosisCryptococcosis/therapyMycologyCryptococcosis is a disease caused by fungi of the genus Cryptococcus, with the species Cryptococcus neoformans and Cryptococcus gattii being recognized as pathogenic. Cutaneous cryptococcosis can be classified as “secondary”, developing from a previous systemic disease, or, on the contrary, “primary”, resulting from transcutaneous inoculation of the agent. It can also be classified as “disseminated cutaneous cryptococcosis”, when there is an associated systemic disease, or “localized”, when it is restricted to the skin. This article uses the term “primary cutaneous cryptococcosis” because it is the most widely used and already established in the literature. Historically, the first report of a possible case of primary cutaneous cryptococcosis (PCC) occurred in 1950 by Gancy WM and was published in the Archives of Dermatology and Syphilology. Subsequently, the rare and sporadic reports in the following decades were reviewed and reported in the 1985 publication by Baes & van Cutsen. However, the unequivocal acceptance of the existence of PCC as a distinct disease only occurred in 2003 with the publication by Neville S et al. of the French Cryptococcosis Study Group. The fundamental criterion established to consider it as PCC was the proven absence of systemic disease, whether pulmonary, in the CNS or other location at the time of diagnosis of the cutaneous condition, characterized by a single lesion and, mostly, in an exposed area. These and other clinical criteria, diagnostic confirmation, and therapeutic choice are discussed in detail in the full text.Department of Infectology Dermatology Diagnostic Imaging and Radiotherapy Faculty of Medicine Universidade Estadual Paulista, SPDepartment of Infectology Dermatology Diagnostic Imaging and Radiotherapy Faculty of Medicine Universidade Estadual Paulista, SPUniversidade Estadual Paulista (UNESP)Marques, Sílvio Alencar [UNESP]Camargo, Rosangela Maria Pires de [UNESP]2025-04-29T19:29:35Z2025-01-01info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/article12-21http://dx.doi.org/10.1016/j.abd.2024.07.004Anais Brasileiros de Dermatologia, v. 100, n. 1, p. 12-21, 2025.1806-48410365-0596https://hdl.handle.net/11449/30343910.1016/j.abd.2024.07.0042-s2.0-85209083445Scopusreponame:Repositório Institucional da UNESPinstname:Universidade Estadual Paulista (UNESP)instacron:UNESPengAnais Brasileiros de Dermatologiainfo:eu-repo/semantics/openAccess2025-04-30T14:08:58Zoai:repositorio.unesp.br:11449/303439Repositório InstitucionalPUBhttp://repositorio.unesp.br/oai/requestrepositoriounesp@unesp.bropendoar:29462025-04-30T14:08:58Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP)false
dc.title.none.fl_str_mv Primary cutaneous cryptococcosis – History, concepts, clinical and therapeutic update
title Primary cutaneous cryptococcosis – History, concepts, clinical and therapeutic update
spellingShingle Primary cutaneous cryptococcosis – History, concepts, clinical and therapeutic update
Marques, Sílvio Alencar [UNESP]
Clinical medicine
Cryptococcosis
Cryptococcosis/diagnosis
Cryptococcosis/therapy
Mycology
title_short Primary cutaneous cryptococcosis – History, concepts, clinical and therapeutic update
title_full Primary cutaneous cryptococcosis – History, concepts, clinical and therapeutic update
title_fullStr Primary cutaneous cryptococcosis – History, concepts, clinical and therapeutic update
title_full_unstemmed Primary cutaneous cryptococcosis – History, concepts, clinical and therapeutic update
title_sort Primary cutaneous cryptococcosis – History, concepts, clinical and therapeutic update
author Marques, Sílvio Alencar [UNESP]
author_facet Marques, Sílvio Alencar [UNESP]
Camargo, Rosangela Maria Pires de [UNESP]
author_role author
author2 Camargo, Rosangela Maria Pires de [UNESP]
author2_role author
dc.contributor.none.fl_str_mv Universidade Estadual Paulista (UNESP)
dc.contributor.author.fl_str_mv Marques, Sílvio Alencar [UNESP]
Camargo, Rosangela Maria Pires de [UNESP]
dc.subject.por.fl_str_mv Clinical medicine
Cryptococcosis
Cryptococcosis/diagnosis
Cryptococcosis/therapy
Mycology
topic Clinical medicine
Cryptococcosis
Cryptococcosis/diagnosis
Cryptococcosis/therapy
Mycology
description Cryptococcosis is a disease caused by fungi of the genus Cryptococcus, with the species Cryptococcus neoformans and Cryptococcus gattii being recognized as pathogenic. Cutaneous cryptococcosis can be classified as “secondary”, developing from a previous systemic disease, or, on the contrary, “primary”, resulting from transcutaneous inoculation of the agent. It can also be classified as “disseminated cutaneous cryptococcosis”, when there is an associated systemic disease, or “localized”, when it is restricted to the skin. This article uses the term “primary cutaneous cryptococcosis” because it is the most widely used and already established in the literature. Historically, the first report of a possible case of primary cutaneous cryptococcosis (PCC) occurred in 1950 by Gancy WM and was published in the Archives of Dermatology and Syphilology. Subsequently, the rare and sporadic reports in the following decades were reviewed and reported in the 1985 publication by Baes & van Cutsen. However, the unequivocal acceptance of the existence of PCC as a distinct disease only occurred in 2003 with the publication by Neville S et al. of the French Cryptococcosis Study Group. The fundamental criterion established to consider it as PCC was the proven absence of systemic disease, whether pulmonary, in the CNS or other location at the time of diagnosis of the cutaneous condition, characterized by a single lesion and, mostly, in an exposed area. These and other clinical criteria, diagnostic confirmation, and therapeutic choice are discussed in detail in the full text.
publishDate 2025
dc.date.none.fl_str_mv 2025-04-29T19:29:35Z
2025-01-01
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
dc.type.driver.fl_str_mv info:eu-repo/semantics/article
format article
status_str publishedVersion
dc.identifier.uri.fl_str_mv http://dx.doi.org/10.1016/j.abd.2024.07.004
Anais Brasileiros de Dermatologia, v. 100, n. 1, p. 12-21, 2025.
1806-4841
0365-0596
https://hdl.handle.net/11449/303439
10.1016/j.abd.2024.07.004
2-s2.0-85209083445
url http://dx.doi.org/10.1016/j.abd.2024.07.004
https://hdl.handle.net/11449/303439
identifier_str_mv Anais Brasileiros de Dermatologia, v. 100, n. 1, p. 12-21, 2025.
1806-4841
0365-0596
10.1016/j.abd.2024.07.004
2-s2.0-85209083445
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv Anais Brasileiros de Dermatologia
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv 12-21
dc.source.none.fl_str_mv Scopus
reponame:Repositório Institucional da UNESP
instname:Universidade Estadual Paulista (UNESP)
instacron:UNESP
instname_str Universidade Estadual Paulista (UNESP)
instacron_str UNESP
institution UNESP
reponame_str Repositório Institucional da UNESP
collection Repositório Institucional da UNESP
repository.name.fl_str_mv Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP)
repository.mail.fl_str_mv repositoriounesp@unesp.br
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