Results 61 to 70 of about 23,997 (201)
American Journal of Pathology, 2021 The u-serrated immunodeposition pattern in direct immunofluorescence (DIF) microscopy is a recognizable feature and confirmative for diagnosis of epidermolysis bullosa acquisita (EBA).
Chenyu Shi +5 more
semanticscholar +1 more source
Epidermolysis Bullosa Acquisita: Ultrastructural and Immunological Studies [PDF]
, 1981 Four patients with epidermolysis bullosa acquisita were investigated using immunofluorescence, routine electron microscopic and immunoelectron microscopic techniques. Immunofluorescence studies demonstrated linear immunoglobulin and complement deposition
Katz, Stephen +8 more
core +1 more source
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
doaj +1 more source
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
doaj +1 more source
Phospholipase Cγ2 is essential for experimental models of epidermolysis bullosa acquisita.
Journal of Investigative Dermatology, 2021 Phospholipase Cγ2 (PLCγ2) mediates tyrosine kinase-coupled receptor signaling in various hematopoietic lineages. Although PLCγ2 has been implicated in certain human and mouse inflammatory disorders, its contribution to autoimmune and inflammatory skin ...
K. Szilveszter +5 more
semanticscholar +1 more source
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
doaj +1 more source
Pemphigoid diseases in infancy and childhood. A review of the literature
Przegląd Dermatologiczny, 2023 Bullous pemphigoid is an autoimmune blistering disease that very rarely affects children. Clinical differences in locations of skin lesions led to the distinction of infantile versus childhood pemphigoid. Mucous membranes can be affected.
Magdalena Jałowska +2 more
doaj +1 more source
Acta Dermato-Venereologica, 2018 Circulating anti-type VII collagen autoantibodies are frequently detected in patients with recessive dystrophic epidermolysis bullosa (RDEB). However, evidence supporting their pathogenic role in inducing epidermolysis bullosa acquisita (EBA) has been ...
Liliana Guerra +6 more
doaj +1 more source
Anais Brasileiros de Dermatologia, 2009 Apresenta-se caso de epidermólise bolhosa adquirida inflamatória. Paciente do sexo masculino, 53 anos, há seis meses com erupção vesicobolhosa pruriginosa sobre base eritematosa no tronco, axilas e membros.
Marcelo D'Ambrosio Fernandes +4 more
doaj +1 more source