Acral persistent papular mucinosis (Q101906): Difference between revisions

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Mucinose papulosa acral persistente é uma forma crônica rara de líquen mixedematoso localizado, caracterizada pelo desenvolvimento de múltiplas pápulas mucinosas simétricas da cor da pele, exclusivamente na face extensora de mãos e antebraços distais.
description / endescription / en
 
Acral persistent papular mucinosis is a rare chronic form of localised lichen myxedematosus characterised by the development of multiple symmetrical skin-coloured mucinous papules exclusively on the extensor surface of the hands and distal forearms.
Property / Canonical URI
 
Property / Canonical URI: https://id.who.int/icd/entity/712202928 / rank
 
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Property / CURIE
 
CID11:ID_712202928
Property / CURIE: CID11:ID_712202928 / rank
 
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Property / Canary Token
 
dki-india-ID_712202928
Property / Canary Token: dki-india-ID_712202928 / 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
 
15 August 2026
Timestamp+2026-08-15T00:00:00Z
Timezone+00:00
CalendarGregorian
Precision1 day
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After0
Property / Collection date: 15 August 2026 / rank
 
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Latest revision as of 18:45, 16 August 2026

Acral persistent papular mucinosis is a rare chronic form of localised lichen myxedematosus characterised by the development of multiple symmetrical skin-coloured mucinous papules exclusively on the extensor surface of the hands and distal forearms.
Language Label Description Also known as
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ID_712202928
    English
    Acral persistent papular mucinosis
    Acral persistent papular mucinosis is a rare chronic form of localised lichen myxedematosus characterised by the development of multiple symmetrical skin-coloured mucinous papules exclusively on the extensor surface of the hands and distal forearms.

      Statements

      CID11:ID_712202928
      0 references
      dki-india-ID_712202928
      0 references
      Concluído
      0 references
      15 August 2026
      0 references