Epidermolysis Bullosa Puriginosa is a genetic mechanobullous disease characterized by pruritus, lichenified or nodular prurigo-like lesions, occasional trauma-induced blistering, excoriations, milia, nail dystrophy and albopapuloid lesions that appear at birth or later. Scarring and prurigo are most prominent on the shins. Herein, we report a case with a history of blisters since childhood followed by intensely pruritic lesions predominantly on the shins and dystrophy of the toenails, milia, excoriations and diffuse post-lesional hyper and hypopigmentation.
Simin Shamsi,M. , Shahriar,D. and Hamidreza,S. (2010). Epidermolysis Bullosa Puriginosa: Report of a Case. Iranian Journal of Dermatology, 13(1), 20-23.
MLA
Simin Shamsi,M. , , Shahriar,D. , and Hamidreza,S. . "Epidermolysis Bullosa Puriginosa: Report of a Case", Iranian Journal of Dermatology, 13, 1, 2010, 20-23.
HARVARD
Simin Shamsi M., Shahriar D., Hamidreza S. (2010). 'Epidermolysis Bullosa Puriginosa: Report of a Case', Iranian Journal of Dermatology, 13(1), pp. 20-23.
CHICAGO
M. Simin Shamsi, D. Shahriar and S. Hamidreza, "Epidermolysis Bullosa Puriginosa: Report of a Case," Iranian Journal of Dermatology, 13 1 (2010): 20-23,
VANCOUVER
Simin Shamsi M., Shahriar D., Hamidreza S. Epidermolysis Bullosa Puriginosa: Report of a Case. Iran J Dermatol, 2010; 13(1): 20-23.
