Indian Dermatology Online Journal (Jan 2014)

Epidermolysis bullosa pruriginosa: A report of two cases

  • Varadraj Vasant Pai,
  • Tukaram Sori,
  • Kikkeri Narayanshetty Naveen,
  • Sharatchandra Bhimrao Athanikar,
  • Vijetha Rai,
  • Dinesh Udupi Shastry

DOI
https://doi.org/10.4103/2229-5178.126030
Journal volume & issue
Vol. 5, no. 1
pp. 44 – 47

Abstract

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Epidermolysis bullosa (EB) pruriginosa is a very rare pattern of dystrophic EB caused by type VII collagen gene mutation, with distinctive clinico-pathological features. It is characterized by nodular prurigo-like lichenified lesions, nail dystrophy, and variable presence of albopapuloid lesions. We report two such cases.

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