Squamous cell carcinoma in junctional and dystrophic epidermolysis bullosa

Authors

  • Florian Weber
  • Johann W. Bauer
  • Norbert Sepp
  • W. Högler
  • Wolfgang Salmhofer
  • Helmut Hintner
  • Peter Fritsch

DOI:

https://doi.org/10.1080/000155501750376285

Abstract

We report here on three patients suffering from recessive dystrophic epidermolysis bullosa and one suffering from generalized atrophic benign epidermolysis bullosa, all of whom developed cutaneous squamous cell carcinoma. Our observations and a review of the literature suggest that squamous cell carcinoma in generalized atrophic benign epidermolysis bullosa is very infrequent and has a better outcome compared to skin cancer in recessive dystrophic epidermolysis bullosa. These differences could be explained by the distinct pathophysiology and clinical course of each of these variants of epidermolysis bullosa. In contrast to UV-induced skin cancer, the tumours in epidermolysis bullosa develop on distal extremities at sites of chronic wound healing. The cases reported here underline the exceptional importance of early histopathological assessment of suspicious skin lesions in patients with epidermolysis bullosa.

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Published

2001-05-20

How to Cite

Weber, F., Bauer, J. W., Sepp, N., Högler, W., Salmhofer, W., Hintner, H., & Fritsch, P. (2001). Squamous cell carcinoma in junctional and dystrophic epidermolysis bullosa. Acta Dermato-Venereologica, 81(3), 189–192. https://doi.org/10.1080/000155501750376285

Issue

Section

Articles