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Epidermolysis bullosa pruriginosa: a rare autosomal dominant variant

Sudip Das1, Alok Kumar Roy, Chinmoy Kar

  • 1Department of Skin, STD and Leprosy, Nilratan Sarkar Medical College and Hospital, Kolkata.

Journal of the Indian Medical Association
|January 9, 2008
PubMed

A 35 years female presented with extremely pruritic, violaceous, small vesiculopapular lesions over both shins since 11/12 years of age. The intensity of pruritus slightly descreased following oozing of fluid. History of similar incidence in her mother and maternal grandfather was present. There was no toe-nail dystrophy. Histopathology report showed the lesions had hyperkeratotic, mild acanthosis, dermal lymphohistiocytic infiltrate and subepidermal cleft. The case was diagnosed to be a case of epidermolysis bullosa pruriginosa.

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