Familial keratoacanthoma
ORPHA:493· ICD-10 L85.8
Definition
A rare inherited skin cancer syndrome characterized by the coexistence of features typical of both multiple self-healing squamous epithelioma and generalized eruptive keratoacanthoma, such as multiple small miliary-type lesions, larger self-healing lesions, and nodulo-ulcerative lesions. Lesions do not have a predilection for the mucosal surfaces.
- Prevalence
- Unknown
- Inheritance
- Autosomal dominant
- Age of onset
- All ages