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Information Journal Paper

Title

PRETIBIAL EPIDERMOLYSIS BULLOSA: REPORT OF TWO CASES

Pages

  39-46

Abstract

 Pretibial epidermolysis bullosa is a rare variant of hereditary epidermolysis bullosa characterized by the delayed onset of lesions andtheir 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 iil 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 unusual, poorly recongnized form of dystrophic epidermolysis bullosa with features that resemble a variety of acquired dermatoses.

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    APA: Copy

    YAGHOUBI, R., SINA, N., EMAD MOSTOJI, N., & RAJIEI, R.. (2004). PRETIBIAL EPIDERMOLYSIS BULLOSA: REPORT OF TWO CASES. IRANIAN JOURNAL OF DERMATOLOGY, 8(Supplement 1), 39-46. SID. https://sid.ir/paper/57901/en

    Vancouver: Copy

    YAGHOUBI R., SINA N., EMAD MOSTOJI N., RAJIEI R.. PRETIBIAL EPIDERMOLYSIS BULLOSA: REPORT OF TWO CASES. IRANIAN JOURNAL OF DERMATOLOGY[Internet]. 2004;8(Supplement 1):39-46. Available from: https://sid.ir/paper/57901/en

    IEEE: Copy

    R. YAGHOUBI, N. SINA, N. EMAD MOSTOJI, and R. RAJIEI, “PRETIBIAL EPIDERMOLYSIS BULLOSA: REPORT OF TWO CASES,” IRANIAN JOURNAL OF DERMATOLOGY, vol. 8, no. Supplement 1, pp. 39–46, 2004, [Online]. Available: https://sid.ir/paper/57901/en

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