OMSB Dermatology (OED) flashcards
OMSB Dermatology (OED) · Build recall with a focused review session.
32 cards. Read the term and the definition here. The deck at the top of this page is optional.
- Pemphigus vulgaris
- Autoimmune blistering disease with IgG antibodies against desmoglein 3, causing suprabasal acantholysis; direct immunofluorescence shows intercellular IgG and C3 in the epidermis.
- Bullous pemphigoid
- Subepidermal blistering disease with linear IgG and C3 along the basement membrane zone; targets BP180 and BP230; tense blisters in elderly patients.
- Dermatitis herpetiformis
- Pruritic vesicular disease with granular IgA at dermal papillae tips; associated with celiac disease; treated with dapsone and gluten-free diet.
- Auspitz sign
- Pinpoint bleeding after removal of scale in psoriasis; reflects dilated capillaries in dermal papillae beneath a thinned suprapapillary plate.
- Koebner phenomenon
- Appearance of new lesions at sites of trauma or injury; classically seen in psoriasis, lichen planus, and vitiligo.
- Wickham striae
- Fine white reticular lines on the surface of lichen planus papules; correspond to hypergranulosis on histology.
- Erythema multiforme
- Targetoid lesions often triggered by HSV infection; Stevens-Johnson syndrome and TEN show mucosal involvement and epidermal detachment, with TEN exceeding 30% body surface area.
- Lupus band test
- Direct immunofluorescence of lesional skin showing granular IgG and C3 at the dermoepidermal junction; supports systemic lupus erythematosus.
- Mohs micrographic surgery
- Margin-controlled excision examining 100% of surgical margins; indicated for high-risk basal cell carcinoma, squamous cell carcinoma, and dermatofibrosarcoma protuberans.
- Breslow thickness
- Measured from the granular layer to the deepest melanoma cell; determines prognosis and surgical margins (1 cm for lesions <=1 mm).
- Sentinel lymph node biopsy
- Procedure to identify the first draining lymph node; considered for melanoma >1 mm Breslow thickness or thinner lesions with ulceration.
- Punch biopsy
- 3-4 mm cylindrical biopsy preserving tissue architecture; preferred for inflammatory dermatoses; shave biopsy is inadequate for assessing depth.
- Sclerotherapy
- Injection of sclerosing agents such as sodium tetradecyl sulfate or polidocanol for telangiectasias; risks include hyperpigmentation and ulceration.
- Cryotherapy
- Liquid nitrogen freezing for warts, actinic keratosis, and seborrheic keratosis; freeze time and thaw cycles determine tissue destruction; risk of hypopigmentation.
- Intralesional corticosteroids
- Triamcinolone 2.5-10 mg/mL injected for keloids, hypertrophic scars, and alopecia areata; higher concentrations risk atrophy.
- Pulsed dye laser
- Laser targeting oxyhemoglobin for vascular lesions such as port-wine stains and telangiectasias; Q-switched lasers target pigment instead.
- Spongiosis
- Intercellular edema in the epidermis; hallmark of eczematous dermatitis such as atopic dermatitis and contact dermatitis.
- Acantholysis
- Loss of intercellular cohesion between keratinocytes; seen in pemphigus vulgaris, Hailey-Hailey disease, and Darier disease.
- Interface dermatitis
- Lymphocytic infiltrate obscuring the dermoepidermal junction; causes include lichen planus, lupus erythematosus, and erythema multiforme.
- Pautrier microabscesses
- Intraepidermal collections of atypical lymphocytes; characteristic of mycosis fungoides and other cutaneous T-cell lymphomas.
- Dermatofibroma
- Dermal spindle cell proliferation with collagen trapping at the periphery; positive for factor XIIIa and negative for CD34.
- Horn pseudocysts
- Keratin-filled cysts within seborrheic keratosis; histology shows basaloid cells without atypia; clinical 'stuck-on' appearance.
- Congo red stain
- Stain for amyloid; under polarized light shows apple-green birefringence; used in macular and lichen amyloidosis.
- Leukocytoclastic vasculitis
- Small vessel vasculitis with fibrinoid necrosis, nuclear dust, and extravasated erythrocytes; presents as palpable purpura.
- Kawasaki disease
- Fever >=5 days with conjunctivitis, oral mucositis, rash, extremity changes, and lymphadenopathy; risk of coronary aneurysms; treated with IVIG and aspirin.
- Hemangioma of infancy
- Vascular tumor proliferating in first months and involuting over years; oral propranolol is first-line for problematic lesions.
- Molluscum contagiosum
- Umbilicated papules caused by a poxvirus; often self-resolving; cantharidin or cryotherapy for persistent lesions.
- Koplik spots
- White lesions on the buccal mucosa preceding the measles rash; rash spreads cephalocaudally.
- Tinea capitis
- Scalp dermatophyte infection, commonly Trichophyton tonsurans in the US; requires oral griseofulvin or terbinafine; topical therapy alone is inadequate.
- Diaper dermatitis
- Irritant contact dermatitis most common; Candida superinfection shows satellite pustules; treat with barrier cream and topical antifungal if candidal.
- Neonatal lupus
- Annular erythematous plaques on face and scalp associated with maternal anti-Ro/SSA antibodies; usually resolves as maternal antibodies clear.
- Topical calcineurin inhibitors
- Tacrolimus and pimecrolimus are steroid-sparing agents for atopic dermatitis; avoid in children under 2 years per labeling.