Indeterminate cell histiocytosis (Q39222): Difference between revisions

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description / pt-brdescription / pt-br
 
Tumor de células dendríticas bastante raro, composto de células fusiformes a ovoides, com fenótipo semelhante ao de células de Langerhans. Manifesta-se, habitualmente, com pápulas, placas e nódulos cutâneos. Sintomas sistêmicos estão geralmente ausentes. O curso clínico é variável.
description / endescription / en
 
A very rare dendritic cell tumour composed of spindle to ovoid cells with a phenotype that is similar to the Langerhans cells. Patients usually present with cutaneous papules, nodules, and plaques. Systemic symptoms are usually absent. The clinical course is variable.
Property / Canonical URI
 
Property / Canonical URI: https://id.who.int/icd/entity/583219258 / rank
 
Normal rank
Property / CURIE
 
CID11:2B31.6
Property / CURIE: CID11:2B31.6 / rank
 
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Property / Canary Token
 
dki-india-2B31.6
Property / Canary Token: dki-india-2B31.6 / 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: C96.4 / rank
 
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Latest revision as of 04:33, 13 August 2026

A very rare dendritic cell tumour composed of spindle to ovoid cells with a phenotype that is similar to the Langerhans cells. Patients usually present with cutaneous papules, nodules, and plaques. Systemic symptoms are usually absent. The clinical course is variable.
Language Label Description Also known as
default for all languages
2B31.6
    English
    Indeterminate cell histiocytosis
    A very rare dendritic cell tumour composed of spindle to ovoid cells with a phenotype that is similar to the Langerhans cells. Patients usually present with cutaneous papules, nodules, and plaques. Systemic symptoms are usually absent. The clinical course is variable.

      Statements

      CID11:2B31.6
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      dki-india-2B31.6
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      Concluído
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      13 August 2026
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      0 references