Doença de Buerger
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Resumo
Objetivo: Identificar, na literatura, informações sobre fisiopatologia, manifestações clínicas e intervenções na Doença de Buerger (DE). Métodos: Trata-se de uma revisão integrativa, realizada por meio dos operadores booleanos “(buerger) AND (vascular) AND (physiopathology OR symptoms OR treatment)” e utilizando as plataformas PubMed, Scielo e Lilacs. Os critérios de inclusão foram: artigos completos e disponíveis gratuitamente; artigos em inglês e português; publicados entre 2020-2023. Adotou-se, como critério de exclusão, artigos que não trouxeram conhecimento para o objetivo proposto. Foram utilizados 30 artigos para este estudo. Resultados: A DE, também conhecida como Tromboangeíte Obliterante (TO), exibe um forte componente imunológico (reações endoteliais e radicais livres). As manifestações clínicas incluem dor, palidez, ulcerações, claudicação intermitente e progressão para amputação. A intervenção baseia-se na cessação do cigarro, porém medicamentos podem ser usados, como antiplaquetários e bloqueadores dos canais de cálcio. Intervenções endovasculares percutâneas apresentam boas chances de melhora, entretanto, a revascularização cirúrgica pode não ser viável, a depender do grau de acometimento vascular. Conclusão: A TO é uma vasculite primária de etiologia desconhecida, cuja sintomatologia é secundária ao dano causado pelo estado inflamatório na parede vascular. O tratamento é complexo, amplo, e deve ser individualizado.
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