Indeterminate cell histiocytosis (Q39222): Difference between revisions
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| description / pt-br | description / 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 / en | description / 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. | |||
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 |
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| 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. |
