Mirizzi Syndrome Type IV: A challenging diagnosis

Autores

  • Daniel Navarini Hospital São Vicente de Paulo Universidade de Passo Fundo
  • Carlos Augusto Scussel Madalosso Hospital São Vicente de Paulo
  • Diego Reffatti Hospital São Vicente de Paulo
  • Luma Guareschi Hospital São Vicente de Paulo
  • Ana Paula Schmitt Hospital São Vicente de Paulo
  • Guilherme Marx Hospital São Vicente de Paulo
  • Paula Jaskulski
  • Henrique Ribeiro Universidade de Passo Fundo
  • Thalis Laydner Hospital São Vicente de Paulo

Palavras-chave:

Mirizzi Syndrome, cholangiocarcinoma, jaundice

Resumo

Mirizzi Syndrome type IV is an extremely rare condition, which is confused with the diagnosis of cholangiocarcinoma in many cases. This report describes a case of a forty-three-year old patient, who was forwarded to our department of general surgery with a high suspicion of a choledochal neoplasic lesion. During the hospitalization he was diagnosed with Mirizzi Syndrome type IV. We concisely describe the case and the literature review about this pathology.

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Publicado

2016-05-18

Como Citar

1.
Navarini D, Scussel Madalosso CA, Reffatti D, Guareschi L, Schmitt AP, Marx G, Jaskulski P, Ribeiro H, Laydner T. Mirizzi Syndrome Type IV: A challenging diagnosis. Clin Biomed Res [Internet]. 18º de maio de 2016 [citado 29º de novembro de 2022];36(1). Disponível em: https://www.seer.ufrgs.br/index.php/hcpa/article/view/60939

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