Conjunctival lymphangioma: a case report and brief review of the literature

Detalhes bibliográficos
Autor(a) principal: Seca, M.
Data de Publicação: 2012
Outros Autores: Borges, P., Gomes, M., Meireles, A.
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
Texto Completo: http://hdl.handle.net/10400.16/1356
Resumo: Background. Lymphangioma is a rare venolymphatic lesion, characterized by dilation of lymphatic vessels. It may occur as an isolated lesion or, more often, represent the surface component of a deep orbital lymphangioma. Case. We report a case of a conjunctival lymphangioma on a 58-year-old male that had simultaneously an upper respiratory tract infection. Excision and biopsy confirmed the nature of the lesion, and there has been no relapse to date. Conclusion. Conjunctival lymphangioma is a rare condition in which the diagnose, must be kept in mind in patients with a red eye resistance to topical therapy and in association with an upper respiratory tract infection. Finally, it is also necessary to be aware of possible recurrence of the lesion.
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spelling Conjunctival lymphangioma: a case report and brief review of the literatureBackground. Lymphangioma is a rare venolymphatic lesion, characterized by dilation of lymphatic vessels. It may occur as an isolated lesion or, more often, represent the surface component of a deep orbital lymphangioma. Case. We report a case of a conjunctival lymphangioma on a 58-year-old male that had simultaneously an upper respiratory tract infection. Excision and biopsy confirmed the nature of the lesion, and there has been no relapse to date. Conclusion. Conjunctival lymphangioma is a rare condition in which the diagnose, must be kept in mind in patients with a red eye resistance to topical therapy and in association with an upper respiratory tract infection. Finally, it is also necessary to be aware of possible recurrence of the lesion.Hindawi Pub. Corp.Repositório Científico do Centro Hospitalar Universitário de Santo AntónioSeca, M.Borges, P.Gomes, M.Meireles, A.2012-12-26T07:38:15Z20122012-01-01T00:00:00Zinfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articleapplication/pdfhttp://hdl.handle.net/10400.16/1356engCase Rep Ophthalmol Med. 2012;2012:8365732090-6730info: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:RCAAP2023-10-20T10:55:37Zoai:repositorio.chporto.pt:10400.16/1356Portal AgregadorONGhttps://www.rcaap.pt/oai/openaireopendoar:71602024-03-19T20:37:46.724908Repositório 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 Conjunctival lymphangioma: a case report and brief review of the literature
title Conjunctival lymphangioma: a case report and brief review of the literature
spellingShingle Conjunctival lymphangioma: a case report and brief review of the literature
Seca, M.
title_short Conjunctival lymphangioma: a case report and brief review of the literature
title_full Conjunctival lymphangioma: a case report and brief review of the literature
title_fullStr Conjunctival lymphangioma: a case report and brief review of the literature
title_full_unstemmed Conjunctival lymphangioma: a case report and brief review of the literature
title_sort Conjunctival lymphangioma: a case report and brief review of the literature
author Seca, M.
author_facet Seca, M.
Borges, P.
Gomes, M.
Meireles, A.
author_role author
author2 Borges, P.
Gomes, M.
Meireles, A.
author2_role author
author
author
dc.contributor.none.fl_str_mv Repositório Científico do Centro Hospitalar Universitário de Santo António
dc.contributor.author.fl_str_mv Seca, M.
Borges, P.
Gomes, M.
Meireles, A.
description Background. Lymphangioma is a rare venolymphatic lesion, characterized by dilation of lymphatic vessels. It may occur as an isolated lesion or, more often, represent the surface component of a deep orbital lymphangioma. Case. We report a case of a conjunctival lymphangioma on a 58-year-old male that had simultaneously an upper respiratory tract infection. Excision and biopsy confirmed the nature of the lesion, and there has been no relapse to date. Conclusion. Conjunctival lymphangioma is a rare condition in which the diagnose, must be kept in mind in patients with a red eye resistance to topical therapy and in association with an upper respiratory tract infection. Finally, it is also necessary to be aware of possible recurrence of the lesion.
publishDate 2012
dc.date.none.fl_str_mv 2012-12-26T07:38:15Z
2012
2012-01-01T00:00:00Z
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