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

synonyms

• Indeterminate cell histiocytosis
• Indeterminate dendritic cell tumour

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