Hereditary hemorrhagic telangiectasia in a sickle cell trait patient: a report of a rare case with use of nuclear medicine and a literature review

Registro completo de metadados
MetadadosDescriçãoIdioma
Autor(es): dc.creatorKang, Hye Chung-
Autor(es): dc.creatorPereira, Miguel Augusto Martins-
Autor(es): dc.creatorSilva, Lucas Natã Lessa-
Autor(es): dc.creatorOliveira, Lucas Caetano-
Autor(es): dc.creatorMárvila, Igor Silva-
Data de aceite: dc.date.accessioned2025-08-21T20:12:48Z-
Data de disponibilização: dc.date.available2025-08-21T20:12:48Z-
Data de envio: dc.date.issued2025-06-05-
Data de envio: dc.date.issued2025-06-05-
Data de envio: dc.date.issued2019-
Fonte completa do material: dc.identifierhttps://app.uff.br/riuff/handle/1/38673-
Fonte: dc.identifier.urihttp://educapes.capes.gov.br/handle/capes/1056757-
Descrição: dc.descriptionSim-
Descrição: dc.descriptionObjective: Rare disease Background: Hereditary hemorrhagic telangiectasia (HHT), also known as Rendu-Osler-Weber syndrome, is a rare autosomal dominant disease. Case Report: Here, we report a case of a 49-year-old Brazilian woman with a history of multiple hospitalizations, sometimes lifehreatening anemia, and uncommon clinical manifestations. Conclusions: We provide a brief literature review regarding the most common signs and symptoms, history, diagnosis, and treatment. Special attention is given to the techniques for identifying hemorrhagic areas, to the presence of angiodysplasia in gastric tissue, and the identification of sickle cell trait, this being an unprecedented hematological condition in the presentation of the disease. Thus, further studies on the relationship between sickle cell trait and the syndrome are needed.-
Formato: dc.formatapplication/pdf-
Idioma: dc.languageen-
Publicador: dc.publisherInternational Scientific Information Incorporation-
Relação: dc.relationTHE AMERICAN JOURNAL OF CASE REPORT. New York: International Scientific Information, 2001-., e-ISSN 1941-5923.-
Direitos: dc.rightsOpen Access-
Direitos: dc.rightsCC-BY-SA-
Palavras-chave: dc.subjectAnemia-
Palavras-chave: dc.subjectAnemia ferropriva-
Palavras-chave: dc.subjectTraço falciforme-
Palavras-chave: dc.subjectTelangiectasia hemorrágica hereditária-
Palavras-chave: dc.subjectAnemia-
Palavras-chave: dc.subjectAnemia, Iron-Deficiency-
Palavras-chave: dc.subjectSickle Cell Trait-
Palavras-chave: dc.subjectTelangiectasia, Hereditary Hemorrhagic-
Título: dc.titleHereditary hemorrhagic telangiectasia in a sickle cell trait patient: a report of a rare case with use of nuclear medicine and a literature review-
Tipo de arquivo: dc.typeArtigo de periódico-
Aparece nas coleções:Repositório Institucional da Universidade Federal Fluminense - RiUFF

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