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Hereditary progressive mucinous histiocytosis

ORPHA:158025· ICD-10 D76.3

Definition

Hereditary progressive mucinous histiocytosis is a rare, benign, non-Langerhans cell histiocytosis characterized by childhood or adolescence onset of multiple, small, asymptomatic, slowly progressing, skin-colored to red-brown papules with predilection for the face, dorsal hands, forearms and legs, without associated mucosal or visceral involvement. Histologically, papules are well-circumscribed, unencapsulated, nodular aggregates of histiocytes with abundant mucin in the upper and middermis.

Prevalence
<1 / 1 000 000
Inheritance
Autosomal dominant
Age of onset
Childhood