@article { author = {Yaghoobi, R and Sina, N and Emad Mostofi, N and Rafiei, R}, title = {Pretibial Epidermolysis Bullosa: Report of two cases}, journal = {Iranian Journal of Dermatology}, volume = {8}, number = {suppl}, pages = {39-46}, year = {2004}, publisher = {Iranian Society of Dermatology}, issn = {2717-0721}, eissn = {2717-0721}, doi = {}, abstract = {Pretibial epidermolysis bullosa is a rare variant of hereditary epidermolysis bullosa characterized by the delayed onset of lesions and their localization. We present two cases, a 35-year-old woman and a 21-year-old man. They clinically had pruritus, nodular prurigo-like or lichenified lesions, violaceous scarring, milia, nail dystrophy and in one case albopapuloid lesions on the trunk. Physical signs of disease were first noticed between 3 and 9 years of age. Histologic examination showed a subepidermal blister with milia formation, and a mild mixed inflammatory infiltrate. These patients represent an nusual, poorly recognized form of dystrophic epidermolysis bullosa with features that resemble a variety of acquired dermatoses.}, keywords = {Dystrophic epidermolysis bullosa,Pretibial,Albopapuloid lesions,Anchoring fibrils}, url = {https://www.iranjd.ir/article_98522.html}, eprint = {https://www.iranjd.ir/article_98522_bd0634e2d10256fb97f67e41a0ce3771.pdf} }