Dermatoscopy of facial actinic keratosis, intraepidermal carcinoma, and invasive squamous cell carcinoma: a progression model

J Am Acad Dermatol. 2012 Apr;66(4):589-97. doi: 10.1016/j.jaad.2011.02.011. Epub 2011 Aug 11.

Abstract

Background: Little is known about the dermoscopic features of keratinocyte skin cancer.

Objective: We sought to determine the dermoscopic features of facial actinic keratosis (AK), intraepidermal carcinoma (IEC), moderately to poorly differentiated invasive squamous cell carcinoma (SCC), and well-differentiated SCC of the keratoacanthoma type.

Methods: This was a retrospective analysis of dermoscopic images of histopathologically diagnosed keratinocyte skin cancer.

Results: A total of 243 (70 AK, 71 IEC, 78 SCC, and 24 keratoacanthomas) tumors of the face from 243 patients (mean age: 71.1 years; range: 44-94 years) were analyzed. The majority of patients had a fair skin type, history of melanoma or nonmelanoma skin cancer, and multiple AK. A red pseudonetwork was significantly associated with AK (P < .001), whereas dotted/glomerular vessels, diffuse yellow opaque scales, and microerosions were significantly more prevalent among IEC (P < .001). Hairpin vessels, linear-irregular vessels, targetoid hair follicles, white structureless areas, a central mass of keratin, and ulceration were significantly associated with invasive SCC (P < .001 for all criteria). Similar patterns as in SCC were observed among keratoacanthomas.

Limitations: The retrospective design of our study and the lack of assessment of sensitivity and specificity of the dermoscopic criteria are limitations.

Conclusions: Based on our findings we propose a progression model of facial AK developing into IEC and invasive SCC.

MeSH terms

  • Adult
  • Aged
  • Aged, 80 and over
  • Carcinoma, Squamous Cell / pathology*
  • Dermoscopy*
  • Disease Progression
  • Facial Dermatoses / pathology*
  • Female
  • Humans
  • Keratoacanthoma / pathology*
  • Keratosis, Actinic / pathology*
  • Male
  • Middle Aged
  • Models, Biological
  • Neoplasm Invasiveness
  • Retrospective Studies
  • Skin Neoplasms / pathology*