Bullous Dermatoses and Drug Eruptions Flashcards
Bullous pemphigoid definition
Autoimmune disorder with autoantibodies against hemidesmosomes (BP230 and BP150)
Bullous pemphigoid symptoms
Acute pruritic tense bullae filled with clear fluid on normal to erythematous skin, bullae do not rupture and heal without scarring
Bullous pemphigoid locations
Inner thigh, flexor forearms, axilla, groin, lower abdomen
Bullous pemphigoid histology
Subepidermal blister with eosinophils
Pemphigus vulgaris definition
Secondary to autoantibodies to components of desmosomes (desmogleins 1 and 3)
Pemphigus vulgaris symptoms
Flaccid bullae with erosion, oral involvement positive Nikolsky’s sign (red skin, fluid collects underneath, skin rubs off, leaves raw red base)
Pemphigus vulgaris histology
Basal cells not attached to each other but still to dermis (tombstone appearance), suprabasal (intraepidermal) blister
Pemphigus vulgaris vs bullous pemphigoid age affected
P. vulgaris - younger, B. pemphigoid - elderly
Pemphigus vulgaris vs bullous pemphigoid oral involvement
P. vulgaris - yes, B. pemphigoid - no
Pemphigus vulgaris vs bullous pemphigoid antibodies
P. vulgaris - against desmoglein 3 (desmosomes), B. pemphigoid - hemidesmosomes
Pemphigus vulgaris vs bullous pemphigoid blister characteristics
P. vulgaris - intraepidermal (superficial), flaccid, rupture easily, B. pemphigoid - subepidermal (deep), tense and firm
Pemphigus vulgaris vs bullous pemphigoid Nikolsky’s sign
P. vulgaris - positive, B. pemphigoid - negative
Pemphigus vulgaris vs bullous pemphigoid immunofluorescence
P. vulgaris - net like IgG, B. pemphigoid - linear IgG
Pemphigus vulgaris vs bullous pemphigoid prognosis
P. vulgaris - pt dies without treatment, B. pemphigoid - most pts do well
Pemphigus vulgaris vs bullous pemphigoid histology
P. vulgaris - tombstone appearance, B. pemphigoid - eosinophilic infiltrations
Urticarial eruptions definition
“Hives”, pruritic eruption, transient, following drug exposure
Urticarial eruptions possible associated symptoms
Angioedema, respiratory symptoms, anaphylaxis
Urticarial eruptions histology
Superficial dermal edema, dilated blood vessels with perivascular inflammatory cells, normal epidermis
Morbilliform eruptions definition
Truly maculopapular, monomorphic, measles-like eruptions following drug exposure
Urticarial eruptions timing
7-10 days after drug exposure, earlier if repeat exposure
Morbilliform eruptions associated symptoms
Systemic symptoms, fever, malaise
Morbilliform eruptions timing
7-10 days after drug exposure (typically antibiotics)
Morbilliform eruptions histology
Indistinguishable from a viral exanthema
Erythema multiforme definition
Self-limited hypersensitivity usually induced by HSV1
Erythema multiforme symptoms
Mouth swelling, painful sores, targetoid, circinate bullae on palms
Erythema multiforme age
Kids and young adults
Erythema multiforme associated symptoms
Rare systemic symptoms, common oral lesions
Erythema multiforme histology
Light lichenoid infiltrate, apoptosis keratinocyte (Colloid body), extensive vacuolar damage at the basement membrane
Urticaria vs erythema multiforme central zones
Urticaria - normal skin, EM - damaged skin (dusky, bullous or crusted)
Urticaria vs erythema multiforme lesion duration
Urticaria - transiet, lasting several hours, EM - fixed for at least 7 days
Urticaria vs erythema multiforme lesion appearance
Urticaria - new lesions appear daily, EM - all lesions appear in first 72 hours
Urticaria vs erythema multiforme edema
Urticaria - swelling of hands and feet (angioedema), EM - no edema
Stevens-Johnson syndrome/toxic epidermal necrosis definition
Hypersensitivity disorder secondary to viral illness, Mycoplasma, medication, or other
Stevens-Johnson syndrome/toxic epidermal necrosis associated symptoms
Fever, systemic symptoms, mucosal erosions, epidermal detachment
Stevens-Johnson syndrome/toxic epidermal necrosis difference
Erosions + epidermal detachment <10% SJS, 10-30% overlap, >30% TEN, SJS more common in kids than TEN
Stevens-Johnson syndrome/toxic epidermal necrosis presenting signs
Fever, malaise, mucosal pain/swelling, photophobia, erythematous macular eruption
Stevens-Johnson syndrome/toxic epidermal necrosis common meds
Anti-epileptics, sulfonamides, PCNs, allopurinol, NSAIDs
Stevens-Johnson syndrome/toxic epidermal necrosis management
Rapidly evolves (mortality is almost 30%), needs monitoring in ICU, ophthalmic evaluation, fluid management, dressings, pain control
Stevens-Johnson syndrome/toxic epidermal necrosis treatment
IVIG, cyclosporine, steroids, TNF-alpha inhibitors