Congenital candidiasis – a diagnostic challenge
Autor(a) principal: | |
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Data de Publicação: | 2021 |
Outros Autores: | , , , , , |
Tipo de documento: | Artigo |
Idioma: | eng |
Título da fonte: | Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) |
Texto Completo: | http://hdl.handle.net/10400.16/2504 |
Resumo: | Introduction: Congenital candidiasis is a rare intrauterine infection characterized by vesicular and pustular skin lesions appearing in the first six days of life. Clinical case: The authors describe the case of a full-term infant presenting erythematous macules, vesicles and pustules involving the trunk and extremities and cervical burn-like dermatitis at birth. Mycological skin lesion culture was positive for Candida albicans. Blood culture was positive for methicillin-sensitive Staphylococcus aureus. After systemic antifungal and antibiotic therapy was started, the newborn remained asymptomatic with lesion improvement. Discussion/ Conclusion: Herein is reported a case of congenital candidiasis in a full-term infant, with a successful recovery. The rarity of congenital candidiasis can lead to delayed diagnosis and unnecessary treatment. This case shows that fungal infection should be considered in the differential diagnosis of vesiculopustular skin lesions in neonates. Systemic therapy should be initiated if invasive candidiasis is suspected. |
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Congenital candidiasis – a diagnostic challengeCandidíase congénita – um desafio diagnósticocandidiasisinvasive fungal diseasesneonateIntroduction: Congenital candidiasis is a rare intrauterine infection characterized by vesicular and pustular skin lesions appearing in the first six days of life. Clinical case: The authors describe the case of a full-term infant presenting erythematous macules, vesicles and pustules involving the trunk and extremities and cervical burn-like dermatitis at birth. Mycological skin lesion culture was positive for Candida albicans. Blood culture was positive for methicillin-sensitive Staphylococcus aureus. After systemic antifungal and antibiotic therapy was started, the newborn remained asymptomatic with lesion improvement. Discussion/ Conclusion: Herein is reported a case of congenital candidiasis in a full-term infant, with a successful recovery. The rarity of congenital candidiasis can lead to delayed diagnosis and unnecessary treatment. This case shows that fungal infection should be considered in the differential diagnosis of vesiculopustular skin lesions in neonates. Systemic therapy should be initiated if invasive candidiasis is suspected.Centro Hospitalar Universitário do PortoRepositório Científico do Centro Hospitalar Universitário de Santo AntónioRolim, SaraFigueirinha, JoanaMiguel, CristinaLopes, SusanaRocha, FelisbelaMartins, CecíliaCarvalho, Sónia2021-10-04T09:46:49Z2021-032021-03-01T00:00:00Zinfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articleapplication/pdfhttp://hdl.handle.net/10400.16/2504engRolim S, Figueirinha J, Miguel C, Lopes S, Rocha F, Martins C, Carvalho S, Nascer e Crescer - Birth and Growth Medical Journal 2021;30(1): 48-51. doi:10.25753/BirthGrowthMJ.v30.i1.200362183-941710.25753/BirthGrowthMJ.v30.i1.20036info:eu-repo/semantics/openAccessreponame:Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)instname:Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informaçãoinstacron:RCAAP2023-10-20T11:00:56Zoai:repositorio.chporto.pt:10400.16/2504Portal AgregadorONGhttps://www.rcaap.pt/oai/openaireopendoar:71602024-03-19T20:38:43.031474Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) - Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informaçãofalse |
dc.title.none.fl_str_mv |
Congenital candidiasis – a diagnostic challenge Candidíase congénita – um desafio diagnóstico |
title |
Congenital candidiasis – a diagnostic challenge |
spellingShingle |
Congenital candidiasis – a diagnostic challenge Rolim, Sara candidiasis invasive fungal diseases neonate |
title_short |
Congenital candidiasis – a diagnostic challenge |
title_full |
Congenital candidiasis – a diagnostic challenge |
title_fullStr |
Congenital candidiasis – a diagnostic challenge |
title_full_unstemmed |
Congenital candidiasis – a diagnostic challenge |
title_sort |
Congenital candidiasis – a diagnostic challenge |
author |
Rolim, Sara |
author_facet |
Rolim, Sara Figueirinha, Joana Miguel, Cristina Lopes, Susana Rocha, Felisbela Martins, Cecília Carvalho, Sónia |
author_role |
author |
author2 |
Figueirinha, Joana Miguel, Cristina Lopes, Susana Rocha, Felisbela Martins, Cecília Carvalho, Sónia |
author2_role |
author author author author author author |
dc.contributor.none.fl_str_mv |
Repositório Científico do Centro Hospitalar Universitário de Santo António |
dc.contributor.author.fl_str_mv |
Rolim, Sara Figueirinha, Joana Miguel, Cristina Lopes, Susana Rocha, Felisbela Martins, Cecília Carvalho, Sónia |
dc.subject.por.fl_str_mv |
candidiasis invasive fungal diseases neonate |
topic |
candidiasis invasive fungal diseases neonate |
description |
Introduction: Congenital candidiasis is a rare intrauterine infection characterized by vesicular and pustular skin lesions appearing in the first six days of life. Clinical case: The authors describe the case of a full-term infant presenting erythematous macules, vesicles and pustules involving the trunk and extremities and cervical burn-like dermatitis at birth. Mycological skin lesion culture was positive for Candida albicans. Blood culture was positive for methicillin-sensitive Staphylococcus aureus. After systemic antifungal and antibiotic therapy was started, the newborn remained asymptomatic with lesion improvement. Discussion/ Conclusion: Herein is reported a case of congenital candidiasis in a full-term infant, with a successful recovery. The rarity of congenital candidiasis can lead to delayed diagnosis and unnecessary treatment. This case shows that fungal infection should be considered in the differential diagnosis of vesiculopustular skin lesions in neonates. Systemic therapy should be initiated if invasive candidiasis is suspected. |
publishDate |
2021 |
dc.date.none.fl_str_mv |
2021-10-04T09:46:49Z 2021-03 2021-03-01T00:00:00Z |
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://hdl.handle.net/10400.16/2504 |
url |
http://hdl.handle.net/10400.16/2504 |
dc.language.iso.fl_str_mv |
eng |
language |
eng |
dc.relation.none.fl_str_mv |
Rolim S, Figueirinha J, Miguel C, Lopes S, Rocha F, Martins C, Carvalho S, Nascer e Crescer - Birth and Growth Medical Journal 2021;30(1): 48-51. doi:10.25753/BirthGrowthMJ.v30.i1.20036 2183-9417 10.25753/BirthGrowthMJ.v30.i1.20036 |
dc.rights.driver.fl_str_mv |
info:eu-repo/semantics/openAccess |
eu_rights_str_mv |
openAccess |
dc.format.none.fl_str_mv |
application/pdf |
dc.publisher.none.fl_str_mv |
Centro Hospitalar Universitário do Porto |
publisher.none.fl_str_mv |
Centro Hospitalar Universitário do Porto |
dc.source.none.fl_str_mv |
reponame:Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) instname:Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informação instacron:RCAAP |
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Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informação |
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RCAAP |
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RCAAP |
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Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) |
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Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) |
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Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) - Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informação |
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1799133647731687424 |