Spontaneous keloids: a rare entity
Autor(a) principal: | |
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Data de Publicação: | 2022 |
Tipo de documento: | Dissertação |
Idioma: | eng |
Título da fonte: | Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) |
Texto Completo: | https://hdl.handle.net/10216/141945 |
Resumo: | Purpose: Keloid scars are a benign fibroproliferative disorder resulting from tissue scar inflammation and abnormal collagen accumulation. Spontaneous keloids occur in the absence of an original traumatic condition, with reported cases associated with several genetic syndromes and a positive family history. This review aims to gather these existing cases, organizing them according to their possible etiology and used treatments. Methods: This review was conducted using PubMed and Web of Science, by using the query ("spontaneous keloids" OR "idiopathic keloids"). No type of filter was applied in the search due to the scarcity of published cases and rarity of this scarring disorder. All case reports and studies related to spontaneous keloids were included and all cases associated with trauma were excluded. In addition, two case reports of this type of keloids were also included. Results: It was possible to verify an association between spontaneous keloids and some genetic disorders. However, there were cases where individuals are completely healthy. Regarding the types of treatment used, it was shown that most keloids remain highly refractory to therapy with high rates of recurrence. Conclusion: Idiopathic keloids are an extremely rare condition whose exact etiology is often difficult to determine, although in certain cases it is possible to verify a probable genetic influence on the origin of this type of scar. Despite its refractoriness, nowadays the combination of surgery and postoperative radiotherapy has shown excellent results. |
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Spontaneous keloids: a rare entityMedicina clínicaClinical medicinePurpose: Keloid scars are a benign fibroproliferative disorder resulting from tissue scar inflammation and abnormal collagen accumulation. Spontaneous keloids occur in the absence of an original traumatic condition, with reported cases associated with several genetic syndromes and a positive family history. This review aims to gather these existing cases, organizing them according to their possible etiology and used treatments. Methods: This review was conducted using PubMed and Web of Science, by using the query ("spontaneous keloids" OR "idiopathic keloids"). No type of filter was applied in the search due to the scarcity of published cases and rarity of this scarring disorder. All case reports and studies related to spontaneous keloids were included and all cases associated with trauma were excluded. In addition, two case reports of this type of keloids were also included. Results: It was possible to verify an association between spontaneous keloids and some genetic disorders. However, there were cases where individuals are completely healthy. Regarding the types of treatment used, it was shown that most keloids remain highly refractory to therapy with high rates of recurrence. Conclusion: Idiopathic keloids are an extremely rare condition whose exact etiology is often difficult to determine, although in certain cases it is possible to verify a probable genetic influence on the origin of this type of scar. Despite its refractoriness, nowadays the combination of surgery and postoperative radiotherapy has shown excellent results.2022-06-032022-06-03T00:00:00Zinfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/masterThesisapplication/pdfhttps://hdl.handle.net/10216/141945TID:203176839engBeatriz Vieira Cabralinfo: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:RCAAP2023-11-29T13:31:50Zoai:repositorio-aberto.up.pt:10216/141945Portal AgregadorONGhttps://www.rcaap.pt/oai/openaireopendoar:71602024-03-19T23:42:01.610106Repositório 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 |
Spontaneous keloids: a rare entity |
title |
Spontaneous keloids: a rare entity |
spellingShingle |
Spontaneous keloids: a rare entity Beatriz Vieira Cabral Medicina clínica Clinical medicine |
title_short |
Spontaneous keloids: a rare entity |
title_full |
Spontaneous keloids: a rare entity |
title_fullStr |
Spontaneous keloids: a rare entity |
title_full_unstemmed |
Spontaneous keloids: a rare entity |
title_sort |
Spontaneous keloids: a rare entity |
author |
Beatriz Vieira Cabral |
author_facet |
Beatriz Vieira Cabral |
author_role |
author |
dc.contributor.author.fl_str_mv |
Beatriz Vieira Cabral |
dc.subject.por.fl_str_mv |
Medicina clínica Clinical medicine |
topic |
Medicina clínica Clinical medicine |
description |
Purpose: Keloid scars are a benign fibroproliferative disorder resulting from tissue scar inflammation and abnormal collagen accumulation. Spontaneous keloids occur in the absence of an original traumatic condition, with reported cases associated with several genetic syndromes and a positive family history. This review aims to gather these existing cases, organizing them according to their possible etiology and used treatments. Methods: This review was conducted using PubMed and Web of Science, by using the query ("spontaneous keloids" OR "idiopathic keloids"). No type of filter was applied in the search due to the scarcity of published cases and rarity of this scarring disorder. All case reports and studies related to spontaneous keloids were included and all cases associated with trauma were excluded. In addition, two case reports of this type of keloids were also included. Results: It was possible to verify an association between spontaneous keloids and some genetic disorders. However, there were cases where individuals are completely healthy. Regarding the types of treatment used, it was shown that most keloids remain highly refractory to therapy with high rates of recurrence. Conclusion: Idiopathic keloids are an extremely rare condition whose exact etiology is often difficult to determine, although in certain cases it is possible to verify a probable genetic influence on the origin of this type of scar. Despite its refractoriness, nowadays the combination of surgery and postoperative radiotherapy has shown excellent results. |
publishDate |
2022 |
dc.date.none.fl_str_mv |
2022-06-03 2022-06-03T00:00:00Z |
dc.type.status.fl_str_mv |
info:eu-repo/semantics/publishedVersion |
dc.type.driver.fl_str_mv |
info:eu-repo/semantics/masterThesis |
format |
masterThesis |
status_str |
publishedVersion |
dc.identifier.uri.fl_str_mv |
https://hdl.handle.net/10216/141945 TID:203176839 |
url |
https://hdl.handle.net/10216/141945 |
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TID:203176839 |
dc.language.iso.fl_str_mv |
eng |
language |
eng |
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info:eu-repo/semantics/openAccess |
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openAccess |
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application/pdf |
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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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