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A Clinical Atlas of 101 Common Skin Diseases

Epidermolysis Bullosa

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A constellation of unrelated blistering diseases, many of them determined genetically but some of them not, that involve skin and sometimes mucous membranes, the blisters often developing after trauma and sometimes resulting in scarring and deformity.

A Clinical Atlas of 101 Common Skin Diseases

Epidermolysis Bullosa

A constellation of unrelated blistering diseases, many of them determined genetically but some of them not, that involve skin and sometimes mucous membranes, the blisters often developing after trauma and sometimes resulting in scarring and deformit…

Therapeutic Strategies in Dermatology

Epidermolysis Bullosa Acquisita

A constellation of unrelated blistering diseases, many of them determined genetically but some of them not, that involve skin and sometimes mucous membranes, the blisters often developing after trauma and sometimes resulting in scarring and deformit…

Therapeutic Strategies in Dermatology

Epidermolysis Bullosa

A constellation of unrelated blistering diseases, many of them determined genetically but some of them not, that involve skin and sometimes mucous membranes, the blisters often developing after trauma and sometimes resulting in scarring and deformit…

Therapeutic Strategies in Dermatology

Epidermolysis Bullosa: Overview

…n. Epidermolysis Bullosa, Junctional All forms of junctional epidermolysis bullosa (JEB) are autosomally recessively inherited. Involvement may be mild (generalized atrophic, localized, and inverse types) or severe (Herlitz and gravis types). System…

Therapeutic Strategies in Dermatology

Bullous Pemphigoid: Overview

…ht in all patients so treated. Other bullous diseases such as epidermolysis bullosa acquisita, erythema multiforme, and bullous drug eruptions may clinically resemble pemphigoid and may explain atypical therapeutic responses. Immunosuppression may re…

Therapeutic Strategies in Dermatology

Epidermolysis Bullosa Acquisita: Overview

Overview Epidermolysis bullosa acquisita (EBA) is an autoimmune disorder due to autoantibodies to Type VII collagen. EBA may present as a noninflammatory bullous lesion with acral distribution that heals with atrophic scarring (similar to porphyria…

Resolving Quandaries in Dermatology, Pathology & Dermatopathology

Acquired Epidermolysis Bullosa?

…20;The “typical” or “average” case of epidermolysis bullosa acquisita may not exist or is at least poorly defined due to the small number of cases accepted as authentic epidermolysis bullosa acquisita.” Woodley DT, Gammo…

Histologic Diagnosis of Inflammatory Skin Diseases

Acquired epidermolysis bullosa

…merated are unique to the diseases grouped under the title of epidermolysis bullosa simplex. Not much can be written about changes histopathologic in the Herlitz type of junctional epidermolysis bullosa because findings when viewed by conventional mi…

Histologic Diagnosis of Inflammatory Skin Diseases

Junctional epidermolysis bullosa

…s for a lifetime, the outcome depending on type of junctional epidermolysis bullosa. (see Variations clinical) Variations clinical Atrophicans generalisata gravis (Herlitz): Onset at birth, blisters widespread, large zones of granulation tissue, C-s…

Histologic Diagnosis of Inflammatory Skin Diseases

Dystrophic epidermolysis bullosa

Dystrophic epidermolysis bullosa Presentation stereotypical Age and sex Infancy, both sexes Distribution of lesions Widespread, but variable according to type of dystrophic epidermolysis bullosa (see Variations clinical) Individual lesions Vesicles,…

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