Type 1 autoimmune pancreatitis: case scenario and review of the disease

Autores/as

  • Jean A. Donet Division of Gastroenterology, University of Miami Leonard Miller School of Medicine, Miami, FL, USA.
  • Frank Czul Division of Gastroenterology, University of Miami Leonard Miller School of Medicine, Miami, FL, USA.
  • Nathalie A. Peña Department of Medicine, University of Miami Leonard Miller School of Medicine, Miami, FL, USA.
  • Jamie S. Barkin Division of Gastroenterology, University of Miami Leonard Miller School of Medicine, Miami, FL, USA.

DOI:

https://doi.org/10.47892/rgp.2016.363.43

Palabras clave:

Pancreatitis, Exocrine pancreatic insufficiency, Cholangitis, sclerosing

Resumen

Autoimmune pancreatitis (AIP) is an uncommon disease that represents a diagnostic challenge unless it is considered as a cause of acute pancreatitis, pancreatic exocrine insufficiency and a pancreatic mass. This entity is under diagnosed and successful medical therapy is available. In this paper, we will describe a case of a 59 year-old, Hispanic woman diagnosed with autoimmune pancreatitis, a disease previously believed to affect typically older men. We will review the definition, types, clinical manifestations, radiological features, serology, histopathological findings, treatment strategies and diagnostic criteria of autoimmune pancreatitis.

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Publicado

03.11.2016

Cómo citar

1.
Donet JA, Czul F, Peña NA, Barkin JS. Type 1 autoimmune pancreatitis: case scenario and review of the disease. Rev Gastroenterol Peru [nternet]. 3 de noviembre de 2016 [citado 25 de abril de 2025];36(3):252-5. isponible en: https://revistagastroperu.com/index.php/rgp/article/view/43

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