Search results
Results from the WOW.Com Content Network
Brunsting–Perry cicatricial pemphigoid is a rare variant of mucous membrane pemphigoid involving the scalp and the neck without mucosal involvement. It is proposed by some authors that this be called a variant of epidermolysis bullosa acquisita .
Gestational pemphigoid: IgG1: NC16A terminal of BPAG2 BPAG1: 180 230 Cicatricial pemphigoid: C-terminal of BPAG2: 180 Ocular cicatricial pemphigoid: Integrin beta-4 subunit: 200 Antiepiligrin cicatricial pemphigoid [nb 1] Laminin 5 (Epiligrin, Laminin 332) Linear IgA bullous dermatosis: LAD1 portion of BPAG2 Collagen type VII: 97 290/145 ...
Localized cicatricial pemphigoid (Brunsting–Perry cicatricial pemphigoid) Paraneoplastic pemphigus; Pemphigus erythematosus (Senear–Usher syndrome) Pemphigus foliaceus; Pemphigus herpetiformis (acantholytic herpetiform dermatitis, herpetiform pemphigus, mixed bullous disease, pemphigus controlled by sulfapyridine) Pemphigoid nodularis ...
Mucous membrane pemphigoid (MMP); also called cicatricial pemphigoid Bullous and mucous membrane pemphigoid usually affect persons who are over age 60. [ 4 ] [ 5 ] Gestational pemphigoid occurs during pregnancy, [ 6 ] typically in the second or third trimester, or immediately following pregnancy.
Antiepilegrin cicatricial pemphigoid: IgG: Dermal Bullous lupus erythematosus: Dermal Bullous pemphigoid: IgG: Epidermal Cicatricial pemphigoid: IgG: Epidermal Epidermolysis bullosa acquisita: IgG: Dermal Linear IgA bullous dermatosis: IgA: Epidermal Orf-induced immunobullous disease: IgG: Dermal Pemphigoid gestationis: IgG: Epidermal
The number of target antigens varies on a case by case basis. The variability is likely what accounts for the different presentations of PNP. Through immunoprecipitation, target antigens have been found to include desmoglein-3, desmoglein-1, envoplakin, periplakin, desmoplakin 1, desmoplakin 2, and bullous pemphigoid antigen I. [citation needed]
The bullae are formed by an immune reaction, initiated by the formation of IgG [citation needed] autoantibodies targeting dystonin, also called bullous pemphigoid antigen 1, [6] and/or type XVII collagen, also called bullous pemphigoid antigen 2, [7] which is a component of hemidesmosomes. A different form of dystonin is associated with ...
This category reflects the organization of International Statistical Classification of Diseases and Related Health Problems, 10th Revision. Generally, diseases outlined within the ICD-10 codes L10–L14 within Chapter XII: Diseases of the skin and subcutaneous tissue should be included in this category.