Results 201 to 210 of about 12,561 (235)
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Erythrodermic bullous pemphigoid
Journal of the American Academy of Dermatology, 1993REFERENCES L Korman N, Pemphigus. J AM ACAD DERMATOL 1988; 18:1219-38. 2. Barthelemy H, Frappaz A, Cambazard F, et al. Treatment of nine cases of pemphigus vulgaris with cyclosporine. J AM ACAD DERMATOL 1988;18:1262-6, 3. ~evuz J. Plasmapheresis. In: Orfanos CE, Stadler R, GollDIck H, eds. Dermatology in five continents.
A, Saitoh +5 more
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Bullous pemphigoid and penicillamine
Clinical and Experimental Dermatology, 1996We describe a woman who developed bullous pemphigoid in association with penicillamine therapy. While pemphigus is a well-recognized complication of penicillamine, pemphigoid should also be considered in the differential diagnosis of bullous eruptions induced by this drug.
R, Weller, M I, White
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Treatment of Bullous Pemphigoid
The Journal of Dermatology, 2003AbstractBullous pemphigoid (BP) is the most frequent auto‐immune blistering skin disease. Up to recently, it was treated with oral corticosteroids. High dose steroids are poorly tolerated in the elderly and probably contributed to the high mortality rates observed in several cohorts.
Juliette, Fontaine +2 more
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Pathogenesis of Bullous Pemphigoid
Dermatologic Clinics, 2011Bullous pemphigoid, the most common autoimmune blistering disease, is induced by autoantibodies against type XVII collagen. Passive transfer of IgG or IgE antibodies against type XVII collagen into animals has revealed not only the pathogenicity of these antibodies but also the subsequent immune responses, including complement activation, mast cell ...
Hideyuki, Ujiie +2 more
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Erythrodermic bullous pemphigoid
International Journal of Dermatology, 2001Case 1 An 87‐year‐old man, with a 2‐year history of a generalized exfoliative erythroderma involving approximately 90% of the body, presented with an onset of tense blisters symmetrically distributed on most of his body.Clinical examination revealed generalized erythema, edema, moderate lichenification, and scaling, with several tense and grouped ...
L. Amato +5 more
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The Pathophysiology of Bullous Pemphigoid
Clinical Reviews in Allergy & Immunology, 2007Bullous pemphigoid (BP) is a blistering skin disease characterized by an autoimmune response to 2 hemidesmosomal proteins within the dermal-epidermal junction, designated BP180 and BP230. While BP230 localizes intracellularly and associates with the hemidesmosomal plaque, BP180 is a transmembrane glycoprotein with an extracellular domain.
Michael, Kasperkiewicz +1 more
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Clinics in Dermatology, 1987
Abstract Dermatologists, with their critical and orderly minds, are ill at ease with a muddle. The classification of the chronic bullous disorders began to appeal to them only when the great controversies of the past seemed to have been settled. Once pemphigoid had been separated from pemphigus and from dermatitis herpetiformis, the subject looked ...
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Abstract Dermatologists, with their critical and orderly minds, are ill at ease with a muddle. The classification of the chronic bullous disorders began to appeal to them only when the great controversies of the past seemed to have been settled. Once pemphigoid had been separated from pemphigus and from dermatitis herpetiformis, the subject looked ...
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Clinics in Dermatology, 1987
Abstract Bullous pemphigoid is a chronic acquired bullous disorder that usually occurs in elderly individuals. In addition to typical clinical features, bullous pemphigoid is also defined by characteristic histopathologic, immunologic, and electromicroscopic criteria.
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Abstract Bullous pemphigoid is a chronic acquired bullous disorder that usually occurs in elderly individuals. In addition to typical clinical features, bullous pemphigoid is also defined by characteristic histopathologic, immunologic, and electromicroscopic criteria.
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