Autoimmune pancreatitis: a case report

Authors

  • E. Valdivielso Cortázar Complejo Hospitalario Universitario de A Coruña
  • C. Prieto Martínez Complejo Hospitalario de Navarra
  • I. Fernández-Urién Complejo Hospitalario de Navarra
  • J. J. Vila Costas Complejo Hospitalario de Navarra
  • F. J. Jiménez Pérez
  • A. Guerra Lacunza Complejo Hospitalario de Navarra

DOI:

https://doi.org/10.23938/S1137-6627/2016000100018

Keywords:

"Autoimmune pancreatitis", "IgG4-related disease"

Abstract

Autoimmune pancreatitis (AIP) is an infrequent pathology, although there is a growing incidence in Eastern countries, which might be due to a greater rate of detection. It can be associated with other autoimmune pathologies and its association with IgG4-related systemic disease has been described. Its clinical presentation is varied and the normal treatment is medical, using corticoids.

A diagnosed clinical case is described.

 

Key words. Autoimmune pancreatitis. IgG4.

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Author Biographies

E. Valdivielso Cortázar, Complejo Hospitalario Universitario de A Coruña

Facultativo Especialista de Área en Aparato Digestivo

C. Prieto Martínez, Complejo Hospitalario de Navarra

Facultativo Especialista de Área

I. Fernández-Urién, Complejo Hospitalario de Navarra

Facultativo Especialista de Área

J. J. Vila Costas, Complejo Hospitalario de Navarra

Facultativo Especialista de Área

A. Guerra Lacunza, Complejo Hospitalario de Navarra

Jefe de Servicio de Aparato Digestivo

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Published

2016-04-29

How to Cite

1.
Valdivielso Cortázar E, Prieto Martínez C, Fernández-Urién I, Vila Costas JJ, Jiménez Pérez FJ, Guerra Lacunza A. Autoimmune pancreatitis: a case report. An Sist Sanit Navar [Internet]. 2016 Apr. 29 [cited 2026 Feb. 21];39(1):149-52. Available from: https://recyt.fecyt.es/index.php/ASSN/article/view/38899

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Section

Clinical notes

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