Pancreatitis autoinmune: a propósito de un caso / Autoimmune pancreatitis: a case report
An. sist. sanit. Navar
; 39(1): 149-152, ene.-abr. 2016.
Article
in Es
| IBECS
| ID: ibc-152697
Responsible library:
ES1.1
Localization: BNCS
RESUMEN
La pancreatitis autoinmune (PAI) es una patología poco frecuente, aunque con una creciente incidencia en países orientales, si bien esto podría deberse a una mayor tasa de detección. Puede asociarse a otras patologías autoinmunes, y se ha descrito su asociación con la enfermedad sistémica por IgG4. La clínica es variada y el tratamiento habitualmente es médico, mediante corticoides. Se describe un caso clínico diagnosticado (AU)
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 (AU)
Full text:
1
Collection:
06-national
/
ES
Database:
IBECS
Main subject:
Pancreatitis
/
Immunoglobulin G
/
Autoimmunity
/
CD4 Immunoadhesins
/
Adrenal Cortex Hormones
Limits:
Adult
/
Humans
/
Male
Language:
Es
Journal:
An. sist. sanit. Navar
Year:
2016
Document type:
Article