Idiopathic copper-associated cirrhosis (Q43607): Difference between revisions

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description / pt-brdescription / pt-br
 
Cirrose idiopática associada ao cobre é uma rara doença hepática rara por sobrecarga de cobre, caracterizada por uma cirrose rapidamente progressiva desde os primeiros anos de vida levando a insuficiência hepática e abrigando um aspecto patológico específico: fibrose pericelular, infiltração inflamatória, necrose de hepatócitos, ausência de esteatose, regeneração deficiente e coloração histoquímica para cobre.
description / endescription / en
 
Idiopathic copper-associated cirrhosis is a rare copper-overload liver disease characterised by a rapidly progressive liver cirrhosis from the first few years of life leading to hepatic insufficiency and harbouring a specific pathological aspect: pericellular fibrosis, inflammatory infiltration, hepatocyte necrosis, absence of steatosis, poor regeneration and histochemical copper staining.
Property / Canonical URI
 
Property / Canonical URI: https://id.who.int/icd/entity/1692504835 / rank
 
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Property / CURIE
 
CID11:DB93.21
Property / CURIE: CID11:DB93.21 / rank
 
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Property / Canary Token
 
dki-india-DB93.21
Property / Canary Token: dki-india-DB93.21 / 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: K74 / rank
 
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Latest revision as of 10:41, 13 August 2026

Idiopathic copper-associated cirrhosis is a rare copper-overload liver disease characterised by a rapidly progressive liver cirrhosis from the first few years of life leading to hepatic insufficiency and harbouring a specific pathological aspect: pericellular fibrosis, inflammatory infiltration, hepatocyte necrosis, absence of steatosis, poor regeneration and histochemical copper staining.
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DB93.21
    English
    Idiopathic copper-associated cirrhosis
    Idiopathic copper-associated cirrhosis is a rare copper-overload liver disease characterised by a rapidly progressive liver cirrhosis from the first few years of life leading to hepatic insufficiency and harbouring a specific pathological aspect: pericellular fibrosis, inflammatory infiltration, hepatocyte necrosis, absence of steatosis, poor regeneration and histochemical copper staining.

      Statements

      CID11:DB93.21
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      dki-india-DB93.21
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      Concluído
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      13 August 2026
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