Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
8715774 | Journal of Dermatology & Dermatologic Surgery | 2017 | 14 Pages |
Abstract
Epidermolysis bullosa pruriginosa, a rare variant of dominant inheritance pattern, characterized by itchy, papules and/or nodules coalescing to form plaque(s), studded by blisters, is describe in a young man an index case. In all 12 afflicted individuals of the 27 family members was interesting, the diagnosis of which was made by its morphology and inflammatory changes in the epidermis, comprising hyperkeratosis, moderate acanthosis, presence of inflammatory cells, and above all inflammatory cell containing sub-epidermal cleavage or cleft.
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Authors
Manisha Nijhawan, Savita Agarwal, Shivi Nijhawan, Rakesh Jhangra, Pallavi Goel, Virendra N. Sehgal,