Results 191 to 200 of about 12,613 (240)
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Journal of the European Academy of Dermatology and Venereology, 2019
AbstractBackgroundBullous pemphigoid (BP) is the most common subepidermal autoimmune blistering disease. Patients occasionally present with a clinical picture of pruritus/urticaria alone for months and do not even develop blisters over time. Only few studies have investigated this subgroup of non‐bullous pemphigoid (NBP).ObjectiveTo evaluate the ...
Y, Ben Mordehai +5 more
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AbstractBackgroundBullous pemphigoid (BP) is the most common subepidermal autoimmune blistering disease. Patients occasionally present with a clinical picture of pruritus/urticaria alone for months and do not even develop blisters over time. Only few studies have investigated this subgroup of non‐bullous pemphigoid (NBP).ObjectiveTo evaluate the ...
Y, Ben Mordehai +5 more
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Erythrodermic bullous pemphigoid is a clinical variant of bullous pemphigoid
British Journal of Dermatology, 1995Bullous pemphigoid (BP) is an autoimmune blistering disease of the skin. Several variants of BP have been described but until recently the relationship of these variants to generalized BP was unclear. Several studies have shown that pemphigoid nodularis, pemphigoid vegetans, localized BP and vesicular pemphigoid are true variants of BP as the ...
N J, Korman, S G, Woods
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The Prodrome of Bullous Pemphigoid
International Journal of Dermatology, 1988ABSTRACT: Bullous pemphigoid is an autoimmune bullous dermatosis that can be preceded by a prodromal phase, usually lasting weeks to months, during which the cutaneous changes are dermatitic rather than bullous. Two cases of unusually long prodromal periods, 18 months and 6 years, are reported.
D A, Amato, J, Silverstein, J, Zitelli
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Dermatologic Clinics, 1987
Bullous pemphigoid is an acquired subepidermal blistering disease of the elderly characterized by tense blisters. Patients with bullous pemphigoid have circulating and tissue-bound antibodies that are directed against a normal component of the epidermal basement membrane.
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Bullous pemphigoid is an acquired subepidermal blistering disease of the elderly characterized by tense blisters. Patients with bullous pemphigoid have circulating and tissue-bound antibodies that are directed against a normal component of the epidermal basement membrane.
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International Journal of Dermatology, 1992
AbstractThree patients had a rare form of bullous pemphigoid, clinically similar to the erythematous type of bullous pemphigoid without vesiculobullous lesions. All the patients displayed immunofluorescence features of bullous pemphigoid. This form of the disease presents a substantial diagnostic problem because it lacks the principal morphologic ...
R, Wolf, J, Ophir, E, Dechner
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AbstractThree patients had a rare form of bullous pemphigoid, clinically similar to the erythematous type of bullous pemphigoid without vesiculobullous lesions. All the patients displayed immunofluorescence features of bullous pemphigoid. This form of the disease presents a substantial diagnostic problem because it lacks the principal morphologic ...
R, Wolf, J, Ophir, E, Dechner
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Interventions for bullous pemphigoid
Cochrane Database of Systematic Reviews, 2023Bullous pemphigoid (BP) is the most common autoimmune blistering disease. Oral steroids are the standard treatment. We have updated this review, which was first published in 2002, because several new treatments have since been tried.To assess the effects of treatments for bullous pemphigoid.We updated searches of the following databases to November ...
Sanjay, Singh +6 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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Bullous pemphigoid in adolescence
Pediatric Dermatology, 2018AbstractBullous pemphigoid (BP) is the most common autoimmune blistering disease affecting the elderly but is quite rare in childhood. The majority of pediatric cases have been reported during early childhood. Adolescence is divided into three phases: early (10‐13 years), middle (14‐17), and late (18‐21).
Aikaterini Patsatsi +2 more
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Eosinophils in bullous pemphigoid
Panminerva Medica, 2021Bullous pemphigoid (BP) is an autoimmune blistering disorder with substantial morbidity and mortality. BP is regarded as a disorder driven by IgG due to BP180 and BP230 IgG autoantibodies, yet, new advances highlight the function of eosinophils and IgE autoantibodies in BP.
Virginia A, Jones +2 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
Maruska, Marovt +1 more
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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
Maruska, Marovt +1 more
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