AOBD Dermatology flashcards
AOBD Dermatology · Build recall with a focused review session.
33 cards. Read the term and the definition here. The deck at the top of this page is optional.
- Auspitz sign
- Pinpoint bleeding that occurs when scale is removed from a psoriasis plaque, reflecting thinned suprapapillary epidermis over dilated dermal capillaries.
- Nikolsky sign
- Separation of the epidermis with gentle lateral pressure, indicating intraepidermal cleavage; positive in pemphigus vulgaris and staphylococcal scalded skin syndrome.
- Pemphigus vulgaris DIF
- Direct immunofluorescence shows intercellular IgG deposits in a net-like pattern within the epidermis, consistent with desmoglein autoantibodies.
- Bullous pemphigoid DIF
- Direct immunofluorescence demonstrates linear deposits of IgG and C3 along the basement membrane zone, indicating autoantibodies against hemidesmosomal proteins.
- Dermatitis herpetiformis DIF
- Granular IgA deposits in dermal papillae are characteristic; associated with gluten-sensitive enteropathy and treated with dapsone or gluten-free diet.
- Basal cell carcinoma features
- Pearly papule with telangiectasia and rolled border; nodular, superficial, and morpheaform subtypes exist; locally invasive but rarely metastasizes.
- Melanoma ABCDE criteria
- Asymmetry, Border irregularity, Color variation, Diameter greater than 6 mm, and Evolving lesion guide clinical recognition of melanoma.
- Miliaria crystallina
- Obstruction of eccrine ducts at the stratum corneum produces clear superficial vesicles without inflammation, often in neonates.
- Miliaria rubra
- Deeper eccrine duct obstruction in the epidermis causes erythematous papulovesicles, commonly in skin folds and occluded areas.
- Erythema toxicum neonatorum
- Blotchy erythema with pustules containing eosinophils appearing in the first days of life; self-limited and requires no treatment.
- Transient neonatal pustular melanosis
- Pustules present at birth that rupture to leave hyperpigmented macules with collarette scale; benign and self-resolving without therapy.
- Kawasaki disease criteria
- Fever for at least 5 days plus 4 of 5 features: rash, conjunctivitis, oral changes, extremity changes, cervical lymphadenopathy; risk of coronary aneurysms.
- Staphylococcal scalded skin syndrome
- Exfoliative toxin causes superficial epidermal cleavage with Nikolsky-positive desquamation; treated with antibiotics, typically in children.
- Hemangioma of infancy
- Vascular tumor appearing shortly after birth that proliferates then involutes; complications include ulceration and airway obstruction.
- Tinea capitis in children
- Scalp dermatophyte infection, often Trichophyton tonsurans, presenting with scaling, alopecia, or kerion; requires oral antifungal therapy.
- Mohs surgery indication
- Used for basal cell and squamous cell carcinoma in high-risk sites or with aggressive histology, recurrent tumors, and ill-defined borders.
- Mohs margin examination
- Frozen sections examine 100 percent of peripheral and deep margins by mapping and en face sectioning of excised tissue.
- Mohs stages
- Each stage involves excision, mapping, orientation with inks, freezing, sectioning, and microscopic examination, repeated until margins are clear.
- Mohs tissue mapping
- A grid with marks correlates the clinical defect with histologic sections, allowing precise localization of residual tumor.
- Mohs contraindications
- Tumors with extensive subclinical spread or those requiring reconstruction beyond Mohs capability are generally not suitable for Mohs surgery.
- Mohs for melanoma
- May be used with immunohistochemistry such as MART-1 and specialized training to assess margins in melanoma.
- Lichen planus histology
- Hyperkeratosis, wedge-shaped hypergranulosis, saw-tooth rete ridges, and band-like lymphocytic infiltrate at the dermoepidermal junction.
- Psoriasis histology
- Regular acanthosis, thinned suprapapillary plates, parakeratosis, and Munro microabscesses of neutrophils in the stratum corneum.
- Pemphigus histology
- Suprabasal acantholysis with tombstoning of basal cells; direct immunofluorescence shows intercellular IgG deposits.
- Dermatitis herpetiformis histology
- Subepidermal blisters with neutrophilic microabscesses in dermal papillae; direct immunofluorescence shows granular IgA.
- Mycosis fungoides histology
- Epidermotropism of atypical lymphocytes with cerebriform nuclei and Pautrier microabscesses within the epidermis.
- Seborrheic keratosis histology
- Horn cysts, pseudohorn cysts, basaloid cells, and melanin pigment characterize this benign epidermal proliferation.
- Actinic keratosis histology
- Atypical keratinocytes in the lower epidermis with parakeratosis and solar elastosis in the dermis, reflecting chronic sun damage.
- Direct immunofluorescence role
- Essential for autoimmune blistering diseases; the location and pattern (intercellular, linear, or granular) guide the specific diagnosis.
- Psoriasis Koebner phenomenon
- New psoriatic lesions develop at sites of skin trauma, a feature shared with lichen planus and vitiligo.
- Scabies diagnosis
- Mineral oil scraping of burrows in web spaces shows mites, eggs, or scybala; nocturnal pruritus is characteristic and contacts require treatment.
- Kerion
- Boggy inflammatory scalp mass due to dermatophyte infection, often with alopecia; requires oral antifungal therapy to prevent scarring.
- Munro microabscess
- Collection of neutrophils within the stratum corneum, a histologic hallmark of psoriasis seen alongside parakeratosis and acanthosis.