Meymandi Simin Shamsi; Dabiri Shahriar; Shafiei Hamidreza
Volume 13, Issue 1 , 2010, , Pages 20-23
Abstract
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 ...
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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.
S Nasiri; F Mollayi; M Vasheghani Farahani
Volume 3, Issue 4 , 2000, , Pages 34-37
Abstract
Background: Most of patients with bullous pemphigoid are at old age and its differentiation from other bullous diseases is important. There is no report of it in Iran. Objective: This study was done in order to determine clinical and paraclinical features, natural course and response to treatment in ...
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Background: Most of patients with bullous pemphigoid are at old age and its differentiation from other bullous diseases is important. There is no report of it in Iran. Objective: This study was done in order to determine clinical and paraclinical features, natural course and response to treatment in patients with bullous pemphigoid admitted in Loghman Hakim Hospital in 1992-1997. Patients and Methods: This descriptive study was done retrospectively by reviewing the existing files of 17 bullous pemphigoid patients admitted in the skin diseases ward of Loghman Hakim Hospital in Tehran in 1992-1997. The diagnosis was confirmed by histopathological examination in all of the patients. Results: The age range of the patients was 19-80 years; most of them were in the 6th-8th decades. 58.8% of the patients were female. Initial lesions were bullous in 53%, eczematous in 29.4% and erythematous or urticarial in 17.6%. 53% of patients were complaining of pruritus. Mucosal involvement was seen in 47%, all in the oral mucosa; only in one of the patients genital area was also involved. No malignancy was seen. 52% of the patients responded to oral prednisolone alone. None of the patients died from the disease. Conclusion: Iranian bullous pemphigoid patients show similar epidemiologic and clinical features to other parts of world.
