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KERATOACANTHOMA

KERATOACANTHOMAย ย ICD-10: D23.L71

โ€ข KA is a special lesion; formerly considered a pseudocancer, it is now regarded by most as a variant of SCC.
โ€ข A relatively common, rapidly growing epithelial tumor with potential for tissue destruction and (rare) metastasis; however, in most cases there is spontaneous regression.
โ€ข HPV-9, -16, -19, -25, -37 have been identified in KAs; other possible etiologic factors include UVR and chemical carcinogens (pitch, tar).
โ€ข Age of onset over 40 years. Male:female ratio 2:1.
โ€ข A dome-shaped nodule with central keratotic plug (Fig. 11-17). Firm but not hard. Skin-colored, slightly red, brown. Removal of keratotic plaque results in a crater.
โ€ข Predilection for sun-exposed sites.
โ€ข Multiple KAs occur.
โ€ข Spontaneous regression in 6 to 12 months in most cases. However, local or visceral metastases have been detected.
โ€ข Histopathology: Not always possible to rule out highly differentiated SCC.
โ€ข Treatment is by excision.

A B

FIGURE 11-17 โ€ข Keratoacanthoma showing different stages of evolutionโ€‚(A) Initially there is a round domeshaped, very firm nodule, reddish with a central hyperkeratotic plug. This has been partially shed leaving a central crater. (B) Hyperkeratosis has progressed and has now replaced most of the nodule, leaving only a thin rim of tumor tissue in the periphery.