Familial keratoacanthoma

Multiple familial keratoacanthoma (KA) of Witten and Zak is a rare a rare inherited skin cancer syndrome and is characterized by the coexistence of features characteristic of both multiple KA, Ferguson Smith type 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. Transmission is autosomal dominant.

Also known as: hereditary keratoacanthoma, multiple keratoacanthoma

1437 clinical trials for this condition and its sub-types, 0 tagged with Familial keratoacanthoma itself.