Results 201 to 210 of about 16,531 (215)
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Archives of Dermatology, 1986
To the Editor.— We read with interest the article in the September 1985 issue of theArchivesby Goldberg et al 1 concerning the best substrate for bullous pemphigoid (BP) antibodies. Our group completed a similar study in late 1985 that compared BP antibody titers from various skin sites on a monkey with BP antibody titers achieved on monkey esophagus.
Ernst H. Beutner +3 more
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To the Editor.— We read with interest the article in the September 1985 issue of theArchivesby Goldberg et al 1 concerning the best substrate for bullous pemphigoid (BP) antibodies. Our group completed a similar study in late 1985 that compared BP antibody titers from various skin sites on a monkey with BP antibody titers achieved on monkey esophagus.
Ernst H. Beutner +3 more
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The American Journal of Dermatopathology, 2015
Rare clinical variants of bullous pemphigoid (BP) include vesicular BP, dyshidrosiform BP, pemphigoid nodularis, seborrheic BP, pemphigoid vegetans, localized BP, erythrodermic BP, and juvenile BP. To our knowledge, this is the first report of an unusual case of purpuric BP. We present a case of 85-year-old white man who presented with a 2-week history
Laila El Shabrawi-Caelen, Maruska Marovt
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Rare clinical variants of bullous pemphigoid (BP) include vesicular BP, dyshidrosiform BP, pemphigoid nodularis, seborrheic BP, pemphigoid vegetans, localized BP, erythrodermic BP, and juvenile BP. To our knowledge, this is the first report of an unusual case of purpuric BP. We present a case of 85-year-old white man who presented with a 2-week history
Laila El Shabrawi-Caelen, Maruska Marovt
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Archives of Dermatology, 1977
A possible genetic link has been suggested in several dermatologic diseases. An increased incidence of HLA-A10 and HLA-B13 has been reported in pemphigus vulgaris, HLA-B17 and HLA-B13 in psoriasis, and HLA-B5 in Behcet syndrome. 1 HLA-B8 has been reported in 70% to 88% of dermatitis herpetiformis cases and in 90% of adult celiac disease cases, 2 which ...
A. Razzaque Ahmed +3 more
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A possible genetic link has been suggested in several dermatologic diseases. An increased incidence of HLA-A10 and HLA-B13 has been reported in pemphigus vulgaris, HLA-B17 and HLA-B13 in psoriasis, and HLA-B5 in Behcet syndrome. 1 HLA-B8 has been reported in 70% to 88% of dermatitis herpetiformis cases and in 90% of adult celiac disease cases, 2 which ...
A. Razzaque Ahmed +3 more
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International Journal of Dermatology, 2006
AbstractBackground Prodromal bullous pemphigoid (PBP) can be difficult to diagnose. Early recognition in its early stages may decrease the morbidity and progression of the disease. Clinical presentations and current treatments available for PBP will be described.Methods A retrospective review was performed on 53 patients diagnosed with PBP.Results ...
Philina M Lamb +4 more
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AbstractBackground Prodromal bullous pemphigoid (PBP) can be difficult to diagnose. Early recognition in its early stages may decrease the morbidity and progression of the disease. Clinical presentations and current treatments available for PBP will be described.Methods A retrospective review was performed on 53 patients diagnosed with PBP.Results ...
Philina M Lamb +4 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, Detlef Zillikens
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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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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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BULLOUS DERMATITIS AND BULLOUS PEMPHIGOID.
British Journal of Dermatology, 1959openaire +3 more sources