2B31.6 Indeterminate cell histiocytosis
International Classification of Diseases for Mortality and Morbidity Statistics, 11th Revision, v2024-01
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.
postcoordination
Add Stem and/or Extension codes to form a cluster code which adds detail to the condition.
Histopathology - only one may be selected
Has manifestation - multiple selections are allowed
synonyms
- Indeterminate cell histiocytosis
- Indeterminate dendritic cell tumour
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