Results 21 to 30 of about 1,292 (153)
Epidermolysis bullosa acquisita
Dermatology Online Journal, 2007 A 29-year-old woman presented with 8 months of multiple vesicles, erosions, and milia on the dorsa of her hands and feet. Histopathologic examination demonstrated a subepidermal blister, with a paucity of eosinophils and a lack of blood vessel wall thickening or caterpillar bodies.
Stein, Jennifer A, Mikkilineni, Radha
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Epidermolysis bullosa acquisita
Journal of the European Academy of Dermatology and Venereology, 2013 AbstractEpidermolysis bullosa acquisita (EBA) is a chronic autoimmune subepidermal bullous disease with clinical features similar to the genetic form of dystrophic epidermolysis bullosa. EBA is characterized by the presence of autoantibodies against type VII collagen which is a major component of the anchoring fibrils at the dermal‐epidermal junction ...
J H, Kim, S-C, Kim
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Epidermolysis bullosa acquisita
Clinics in Dermatology, 2012 Epidermolysis bullosa acquisita (EBA) is a rare, acquired, chronic subepidermal bullous disease of the skin and mucosa characterized by autoantibodies to type VII collagen (C7) structures, a major component of anchoring fibrils, which attach the epidermis to the dermis.
Rishu, Gupta +2 more
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Epidermolysis bullosa acquisita
Indian Journal of Dermatology, Venereology and Leprology, 2006 A 20 year old male started developing bubae following even minor trauma on the skin as well as the mucous membranes during the preceding 5 years. The bunae healed with atrophic scars. Involvement of the oral mucous membrane and the eyes, scpcially the right eye, was quite extensive and unusual.
Jayanta Kr, Das +2 more
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Epidermolysis bullosa acquisita following skin graft in donor and graft sites: A case report
Burns Open, 2023 Epidermolysis bullosa acquisita is a rare mucocutaneous autoimmune blistering disorder which usually presents in adulthood. The disease is mediated by antibodies against type VII collagen, though the precise inciting factors for autoantibody formation ...
Joyce Xia +6 more
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Dermatologica Sinica, 2011 Antiepiligrin cicatricial pemphigoid (AECP) is a chronic autoimmune subepidermal blistering disease characterized by clinical features of cicatricial pemphigoid and circulating IgG antibasement membrane autoantibodies directed against laminin 332.
Chih-Pin Chen +3 more
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Epidermolysis bullosa acquisita
Der Hautarzt, 2019 Epidermolysis bullosa acquisita (EBA) is a rare acquired subepidermal bullous autoimmune dermatosis, associated with autoantibodies against collagen type VII, the most important component of dermal anchoring fibrils. Blister induction occurs after binding of autoantibodies to collagen type VII, leading to complement activation, recruitment of ...
S C, Hofmann, A, Weidinger
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Diseases presenting with vesicular and erosive lesions of oral mucous membranes
Przegląd Dermatologiczny, 2017 Disorders of the oral mucosa are an area of interdisciplinary cooperation involving physicians from a diverse range of medical specialties.
Kamila Ociepa, Agnieszka Żebrowska
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Generalized erosions, blisters, scarring, and milia in a 65-year-old woman: a diagnostic challenge
Journal of the Egyptian Women’s Dermatologic Society, 2021 Epidermolysis bullosa acquisita (EBA) is a chronic autoimmune subepidermal blistering disease of the skin and mucous membranes. EBA is caused by antibodies targeting type VII collagen, the major component of anchoring fibrils that connects the basement ...
Galal El Enany +8 more
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An 81-Year-Old Woman with Recalcitrant Blisters
Dermatopathology, 2018 Epidermolysis bullosa acquisita (EBA) is a rare mucocutaneous blistering disorder with typical onset in adulthood. Diagnosis and management can be difficult owing to the variability in presentation and clinical manifestation.
Daniel C. Butler
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