Ch. 9 - Blistering diseases Flashcards
What are the subcorneal vesiculbullous disorders?
Pemphigus foliaceus
Subcorneeal pustular dermatosis
Acute generalized exanthematous pustulosis
Pemphigus foliaceus
(cause?)
Subcorneal split with some acantholysis and dyskeratosis. Net-like IgG/C3 in upper epidermis.
(IgG directed at desmoglein 1)
Subcorneal pustular dermatosis (Sneddon-Wilkinson disease)
Subcorneal pustule “sitting” upon epidermis. No dyskeratosis. No immunofluorescence.
Acute generalized exanthematous pustulosis
(cause?)
Subcorneal epidermal pustules with mild spongiosis and occasional eosinophils. No immunofluorescence.
(reaction to antibiotics)
What are the intraepidermal vesiculbullous disorders?
Pemphigus vulgaris
Familial benign chronic pemphigus (Hailey-Hailey disease)
Keratosis follicularis (Darier’s disease)
Transient acantholytic dermatosis (Grover’s disease)
Paraneoplastic pemphigus
Pemphigus vulgaris
(cause?)
Basal layer split with follicular extension. Eosinophils. DIF with IgG/C3 between keratinocytes in lower epidermis.
(IgG against desmoglein 3)
Familial benign chronic pemphigus (Hailey-Hailey disease)
(cause?)
Acanthotic and acantholytic lesion. Red dyskeratotic rim around nucleus. No immunofluorescence.
(inherited mutation in ATP2C1)
Keratosis follicularis (Darier’s disease)
(cause?)
Acantholytic lesion with more dyskeratosis than Hailey-Hailey disease. Grains, corps ronds, blue/clear perinuclear rim, and no immunofluorescence.
(inherited mutation in ATP2A2)
Transient acantholytic dermatosis (Grover’s disease)
Many patterns, including Darier’s, Hailey-Hailey’s, Pemphigus, and Spongiotic. May or may not be transient. Not inherited.
Paraneoplastic pemphigus
(cause?)
Variable intraepidermal acantholysis with lichenoid infiltration. DIF with IgG/C3 linear deposition at junction.
(many possible antibodies)
What are the pauci-inflammatory subepidermal vesiculbullous disorders?
Porphyria cutanea tarda
Epidermolysis bullosa acquisita
TEN/SJS
Porphyria cutanea tarda
Subepidermal vesiculation with solar elastosis, festooning of dermal papillae into vesicle, and caterpillar bodies in the epidermis. DIF with IgM/C3 in vessels.
Epidermolysis bullosa acquisita
(cause?)
Subepidermal vesiculation with fibrin deposition in floor and inflammatory infiltrate. DIF with IgG/C3 at junction, sometimes IgA.
(antibody to type VII collagen)
TEN/SJS
Subepidermal vesiculation and sloughing with confluent epidermal necrosis. Some inflammatory infiltrate. No immunofluorescence.
What are the inflammatory subepidermal vesiculbullous diseases?
Bullous pemphigoid
Cicatricial pemphigoid
Dermatitis herpetiformis
Linear IgA bullous dermatosis
Bullous lupus erythematosis
Friction blister