Autoimmune pancreatitis (Q43689): Difference between revisions
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| description / pt-br | description / pt-br | ||
Pancreatite autoimune (PAI) é uma doença pancreática rara caracterizada por pancreatite crônica não alcoólica que se apresenta com dor abdominal, esteatorreia, icterícia obstrutiva, e responde bem a terapia com esteroides e é observada em duas subformas: PAI tipo 1 que acomete homens idosos, envolve outros órgãos e tem níveis aumentados de imunoglobina G4 (IgG4) e PAI tipo 2 que afeta ambos os sexos igualmente, mas se apresenta em uma idade mais jovem e não tem envolvimento de outros órgãos ou níveis aumentados de IgG4. | |||
| description / en | description / en | ||
Autoimmune pancreatitis (AIP) is a rare pancreatic disease characterised by chronic non-alcoholic pancreatitis that presents with abdominal pain, steatorrhoea, obstructive jaundice and responds well to steroid therapy and is seen in two subforms: type 1 AIP which affects elderly males, involves other organs and has increased immunoglobin G4 (IgG4) levels and type 2 AIP which affects both sexes equally but presents at a younger age and has no other organ involvement or increased IgG4 levels. | |||
Revision as of 10:48, 13 August 2026
Autoimmune pancreatitis (AIP) is a rare pancreatic disease characterised by chronic non-alcoholic pancreatitis that presents with abdominal pain, steatorrhoea, obstructive jaundice and responds well to steroid therapy and is seen in two subforms: type 1 AIP which affects elderly males, involves other organs and has increased immunoglobin G4 (IgG4) levels and type 2 AIP which affects both sexes equally but presents at a younger age and has no other organ involvement or increased IgG4 levels.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | DC33 |
||
| English | Autoimmune pancreatitis |
Autoimmune pancreatitis (AIP) is a rare pancreatic disease characterised by chronic non-alcoholic pancreatitis that presents with abdominal pain, steatorrhoea, obstructive jaundice and responds well to steroid therapy and is seen in two subforms: type 1 AIP which affects elderly males, involves other organs and has increased immunoglobin G4 (IgG4) levels and type 2 AIP which affects both sexes equally but presents at a younger age and has no other organ involvement or increased IgG4 levels. |
