Ad
related to: linear iga bullous dermatosis
Search results
Results From The WOW.Com Content Network
Linear IgA bullous dermatosis is a rare immune-mediated blistering skin disease frequently associated with medication exposure, especially vancomycin, with men and women being equally affected. [ 2 ] : 135 It was first described by Tadeusz Chorzelski in 1979 and may be divided into two types: [ 3 ] : 587
Intraepidermal neutrophilic IgA dermatosis is characterized histologically by intraepidermal bullae with neutrophils, some eosinophils, and acantholysis. [8] The least common and most severe type of pemphigus is paraneoplastic pemphigus (PNP). This disorder is a complication of cancer, usually lymphoma or Castleman's disease. It may precede the ...
Linear IgA bullous dermatosis (linear IgA dermatosis) Photosensitive drug reaction; Red man syndrome; Severe cutaneous adverse reactions (includes DRESS syndrome, Steven Johnson syndrome, Toxic epidermal necrolysis, Stevens-Johnson/toxic epidermal necrolysis overlap syndrome, and Acute generalized exanthematous pustulosis)
Sometimes presence of eosinophils, giving an appearance similar to bullous pemphigoid. [24] The histopathology is unspecific in approximately 35%–40% of the cases, [24] and direct immunofluorescence is needed, showing deposition of IgA in the papillary dermis in a granular or fibrillar pattern. [25] Early linear IgA bullous dermatosis
694 Bullous dermatoses. 694.0 Dermatitis herpetiformis; 694.1 Subcorneal pustular dermatosis; 694.2 Juvenile dermatitis herpetiformis; 694.3 Impetigo herpetiformis; 694.4 Pemphigus; 694.5 Pemphigoid; 694.6 Benign mucous membrane pemphigoid; 694.8 Other specified bullous dermatoses; 694.9 Unspecified bullous dermatoses; 695 Erythematous ...
Antibody isotype(s) and location of antibody deposition in immunofluorescence studies using salt-split skin for autoimmune bullous conditions targeting the basement membrane zone of the human integumentary system Condition Antibody isotype(s) deposited Localization of antibody with use of salt-split skin Antiepilegrin cicatricial pemphigoid ...
Linear IgA disease: Skin Anti-epidermal basement membrane IgA Confirmed Extremely rare [18] Morphea: Skin None specific Probable Not well established [19] Psoriasis: Skin Various, not specific Confirmed 2-3% [20] Pemphigus vulgaris: Skin and mucous membranes Anti-desmoglein 3, Anti-desmoglein 1 Confirmed 1-5 per 100,000 [21] Scleroderma ...
IgA pemphigus is a subtype of pemphigus with two distinct forms: Subcorneal pustular dermatosis (also known as Sneddon–Wilkinson disease and pustulosis subcornealis) [ 1 ] is skin condition that is a rare, chronic, recurrent, pustular eruption characterized histopathologically by subcorneal pustules that contain abundant neutrophils.