Casos Clínicos

Cardiac Amyloidosis, Follow the Trail Not to Miss the Diagnosis

Conteúdo principal do artigo

Silvia Ribeiro
Catarina Vieira
Filipa Cordeiro
João Costa
Palavras-chave:
Amiloidose, Amiloidose de Cadeia Leve de Imunoglobulina, Cardiomiopatias, Neuropatias Amilóides Familiares

Resumo

A amiloidose é uma doença sistémica causada pelo depósito extracelular de fibrilas insolúveis de proteínas de baixo peso molecular, sendo as mais comuns as cadeias leves (amiloidose AL) e a transtirretina (amiloidose ATTR), esta última  sob a forma adquirida (wild type) ou hereditária. Apesar de ser considerada rara, é hoje reconhecido o seu subdiagnóstico, pelo que é fundamental um elevado índice de suspeita no sentido de alterar  a morbilidade e mortalidade dos doentes por ela afetados.


 Os autores descrevem um caso clínico de amiloidose com envolvimento cardíaco.

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Referências

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