Autoimmune pancreatitis (Q43689): Difference between revisions

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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 / endescription / 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.
Property / Canonical URI
 
Property / Canonical URI: https://id.who.int/icd/entity/2057951941 / rank
 
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Property / CURIE
 
CID11:DC33
Property / CURIE: CID11:DC33 / rank
 
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Property / Canary Token
 
dki-india-DC33
Property / Canary Token: dki-india-DC33 / rank
 
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Property / Verification Status
 
Concluído
Property / Verification Status: Concluído / rank
 
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Property / Knowledge Architect
 
Property / Knowledge Architect: https://pauloleads.com.br/cases-publicos/ / rank
 
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Property / Collection date
 
13 August 2026
Timestamp+2026-08-13T00:00:00Z
Timezone+00:00
CalendarGregorian
Precision1 day
Before0
After0
Property / Collection date: 13 August 2026 / rank
 
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Property / Linked ICD 10
 
Property / Linked ICD 10: K86.1 / rank
 
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Latest 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
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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.

      Statements

      CID11:DC33
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      dki-india-DC33
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      Concluído
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      13 August 2026
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