Indeterminate cell histiocytosis (Q39222): Difference between revisions
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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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