Epidermolysis bullosa acquisita

The article describes present-day information on the pathogenesis, clinical picture, treatment and differential diagnostics of epidermolysis bullosa acquisita, an autoimmune skin disease caused by the production of anti-Type VII collagen autoantibodies and manifested mainly by subepidermal blisters...

وصف كامل

التفاصيل البيبلوغرافية
الحاوية / القاعدة:	Vestnik Dermatologii i Venerologii
المؤلفون الرئيسيون:	V. V. Chikin, L. F. Znamenskaya, M. A. Nefedova, V. A. Charikov
التنسيق:	مقال
اللغة:	الإنجليزية
منشور في:	State Scientific Center of Dermatovenereology and Cosmetology 2017-08-01
الموضوعات:	приобретенный буллезный эпидермолиз дифференциальная диагностика непрямая реакция иммунофлюоресценции epidermolysis bullosa acquisita differential diagnostics indirect immunofluorescence
الوصول للمادة أونلاين:	https://www.vestnikdv.ru/jour/article/view/148

مواد مشابهة

Acquired bullous epidermolysis: complexity of diagnostics
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Squamous-cell carcinoma in a female patient suffering from recessive dystrophic epidermolysis bullosa
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Prevalence of hereditary epidermolysis bullosa in the Russian Federation
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Epidermolysis Bullosa Acquisita in Children: Case Series
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Epidermolysis Bullosa Acquisita Occuring In A Patient With Systemic Lupus Erythematosus
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Excellent response to rituximab in a patient with recalcitrant epidermolysis bullosa acquisita: a case report
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Porphyria Cutanea Tarda Masquerading as Epidermolysis Bullosa Acquisita: A Report of Two Cases
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Differentiating antiepiligrin cicatricial pemphigoid from epidermolysis bullosa acquisita by indirect immunofluorescence of skin substrates lacking Type VII collagen or laminin 332: a case report and review of literature
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Kindler syndrome - a rare type of hereditary epidermolysis bullosa
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Inhibition of interferon gamma impairs induction of experimental epidermolysis bullosa acquisita
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IgM-mediated epidermolysis bullosa acquisita
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Case Report: Biological treatment of epidermolysis bullosa acquisita: report on four cases and literature review
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Vesiculobullous Erythema Elevatum Diutinum: A Rare Variant with Epidermolysis Bullosa Acquisita - like Immunofluorescence Findings
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Epidermolysis bullosa acquisita following skin graft in donor and graft sites: A case report
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C-type lectin receptor expression is a hallmark of neutrophils infiltrating the skin in epidermolysis bullosa acquisita
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Therapeutic effects of Fc gamma RIV inhibition are mediated by selectively blocking immune complex-induced neutrophil activation in epidermolysis bullosa acquisita
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Modern methods of the treatment of hereditary epidermolysis bullosa
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Risk factors and sequelae of epidermolysis bullosa acquisita: A propensity-matched global study in 1,344 patients
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Dystrophic epidermolysis bullosa in a child
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“Quality of Life in Epidermolysis Bullosa” and “Epidermolysis Bullosa Burden of Disease”: Italian translation, cultural adaptation, and pilot testing of two disease-specific questionnaires
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Mixed IgM- and IgA-mediated epidermolysis bullosa acquisita associated with IgM-λ paraproteinemia in an 81-year-old woman
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