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The nosological boundaries between EBA and bullous systemic lupus erythematosus see this term remain under debate.

epidermólisis ampollar – English Translation – Word Magic Spanish-English Dictionary

Health care resources for this disease Expert centres Diagnostic tests 6 Patient organisations 8 Orphan drug s 1. Although further trials are necessary, encouraging results have been obtained with other approaches such as intravenous immunoglobulin therapy, extracorporeal photochemotherapy and, more recently, rituximab therapy. Involvement of the mucosae in particular the ocular and ORL mucosal membranes is associated with more severe disease, which may lead to a poorer functional, or even vital, prognosis.

Immunosuppresive therapy such as treatment with cyclosporine may by required in severe cases. Diagnostic methods Diagnosis relies on the results of histological analysis, indirect or ammpollar immunofluorescence studies, immunoblotting and immune electron microscopy.

Other search option s Alphabetical list. Lesions are usually triggered by minor trauma and are mainly localised to sites that are easily injured.

Only comments written in English can be processed. As in dystrophic HEB caused by mutations in the gene encoding collagen VII, the deposition of antibodies on collagen VII leads to cleavage between the epidermis and dermis below the lamina densa.

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Diagnosis relies on the results of histological analysis, indirect or direct immunofluorescence studies, immunoblotting and immune electron microscopy. Additional information Further information on this disease Classification s 1 Gene epidermllisis 0 Clinical signs and symptoms Other website s 4. Disease definition Epidermolysis bullosa acquisita EBA is a subepidermal bullous dermatosis of autoimmune origin that was named as a result of its resemblance to hereditary forms of epidermolysis bullosa HEBmost notably dystrophic HEB.

During the disease course, the inflammatory forms may evolve to resemble the classical form and patients with the classical present with bursts of inflammatory disease. Etiology EBA is caused by the production of antibodies against the skin basement membrane collagen VII, the major component of the anchoring fibrils located in the dermal-epidermal junction, under the lamina densa.

Differential diagnosis The differential diagnosis should include other subepidermal, autoimmune bullous diseases. Summary Epidemiology The prevalence is unknown but the incidence is estimated at 1 in 96, new cases per year. The disease manifests during childhood. Clinical description The disease manifests in two clinical forms: Epidermolysis bullosa acquisita EBA is a subepidermal bullous dermatosis of autoimmune origin that was named as a result of its resemblance to hereditary forms of epidermolysis bullosa HEBmost notably dystrophic HEB.

The material is in no way intended to replace professional medical care by a qualified specialist and should not be used as a basis for diagnosis or treatment. The first line treatment revolves around administration of dapsone or sulfasalazine. For all other comments, please send your remarks via contact us. The disease manifests in two clinical forms: Management and treatment The first line treatment revolves around administration of dapsone or sulfasalazine.

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Summary and related texts. EBA is caused by the production of antibodies against the skin basement membrane collagen VII, the major component of the anchoring fibrils located in the dermal-epidermal junction, under the lamina densa. Only comments seeking to improve the quality and accuracy of information on the Orphanet website are accepted. Check this box if you wish to receive a copy of your message.

Involvement of the mucous membranes, hair and nails is frequent. Epidermolysis bullosa acquisita Prevalence: Specialised Social Services Eurordis directory. In the classical form, onset occurs in adulthood and the bullae may be soft, tense or haemorrhagic, located on otherwise healthy epidermoliisis.

EBA is a chronic disease that resolves slowly and leads to dystrophic scarring and milia.

The inflammatory form was recognised more recently and resembles bullous pemphigoid epideemolisis this term with bullae developing on erythematous skin lesions, plaques without bullous eruptions and diffuse lesions that are not limited to trauma-prone sites. Prognosis EBA is a chronic disease that resolves slowly and leads to dystrophic scarring and milia.