Results 191 to 200 of about 12,561 (235)
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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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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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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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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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Bullous pemphigoid in an infant
Australasian Journal of Dermatology, 1995SUMMARYAn acral blistering eruption in a 10 week old baby was found on histology and direct immunofluorescence to be bullous pemphigoid. Circulating auto‐antibodies were not detected. He responded quickly to oral prednisolone and there have been no sequelae.
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[Physiopathology of bullous pemphigoid].
Annales de dermatologie et de venereologie, 2009International ...
Doffoel-Hantz, V. +5 more
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The immunopathology of bullous pemphigoid
Clinics in Dermatology, 1987Abstract The immunopathology of bullous pemphigoid features basement membrane zone (BMZ) deposition of immunoglobulin and complement and the presence of circulating immunoreactants. 1,2 The demonstration of linear subepidermal deposition of C3 and/or IgG is usually necessary to establish the diagnosis.
M J, Imber, G F, Murphy, R E, Jordon
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Bullous and cicatricial pemphigoid
Journal of Autoimmunity, 1991Bullous pemphigoid (BP) and cicatricial pemphigoid are blistering mucocutaneous diseases characterized by detachment of the overlying epithelium from its stroma. IgG and complement components are deposited in all affected tissue at the level of blister formation--through the lamina lucida of the epithelium. The primary antibody response is of the IgG 4
G J, Anhalt, L H, Morrison
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