ABD Dermatopathology flashcards
ABD Dermatopathology · 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.
- Spongiotic dermatitis
- Microscopic pattern with intercellular edema in the epidermis; eosinophils favor allergic contact or drug reaction, while neutrophils in the stratum corneum suggest impetiginization.
- Lichen planus histology
- Interface dermatitis with wedge-shaped hyperkeratosis, saw-tooth rete ridges, and a bandlike lymphocytic infiltrate obscuring the dermoepidermal junction; PAS highlights basement membrane thickening.
- Pemphigus vulgaris DIF
- Direct immunofluorescence shows intercellular IgG and C3 in the epidermis, producing a chicken-wire pattern; serum antibodies target desmoglein 3.
- Bullous pemphigoid DIF
- Direct immunofluorescence reveals linear IgG and C3 along the basement membrane zone; salt-split skin shows epidermal roof staining, distinguishing it from epidermolysis bullosa acquisita.
- Dermatitis herpetiformis DIF
- Direct immunofluorescence shows granular IgA deposits in dermal papillae; associated with gluten-sensitive enteropathy and celiac disease.
- Leukocytoclastic vasculitis
- Small-vessel vasculitis with fibrinoid necrosis, neutrophilic dust, and extravasated red cells; direct immunofluorescence may show granular IgA in Henoch-Schonlein purpura.
- Sarcoidal granuloma
- Naked noncaseating granulomas with sparse lymphocytic rim in the dermis; seen in sarcoidosis, and Schaumann bodies or asteroid bodies may be present.
- Breslow thickness
- Measured in millimeters from the granular layer of the epidermis to the deepest invasive melanoma cell; used for staging and sentinel node decisions.
- Benign nevus maturation
- Nevus cells become smaller and less nested with increasing dermal depth; lack of maturation and deep mitoses favor melanoma.
- Pagetoid scatter
- Atypical melanocytes spread upward through the epidermis, a feature of melanoma; it can also occur in Spitz nevi and sun-damaged skin.
- HMB-45 expression
- Immunostain marks melanocytic cells and typically diminishes with dermal depth in benign nevi; retained deep expression or PRAME positivity favors melanoma.
- Lentigo maligna
- Melanoma in situ on sun-damaged skin with atypical melanocytes along the dermoepidermal junction; it may progress to invasive lentigo maligna melanoma.
- Spitz nevus
- Benign melanocytic lesion with spindle or epithelioid cells, Kamino bodies, and maturation; atypical Spitz tumors require molecular testing for risk assessment.
- Sentinel lymph node biopsy
- Identifies early nodal melanoma metastasis using immunohistochemistry for S100, SOX10, and Melan-A; positivity affects staging and treatment.
- Actinic keratosis
- Atypical keratinocytes confined to the lower epidermis over sun-damaged skin; full-thickness atypia indicates squamous cell carcinoma in situ.
- Basal cell carcinoma
- Nests of basaloid cells with peripheral palisading, clefting, and mucin; Ber-EP4 immunostain is positive, helping distinguish it from squamous cell carcinoma.
- Keratoacanthoma
- Crateriform squamous proliferation with a central keratin plug and glassy cytoplasm; it may regress spontaneously but can show invasive features.
- Pilomatricoma
- Adnexal tumor with basaloid cells and ghost cells, often with calcification; it typically presents as a firm nodule in children.
- Sebaceous adenoma
- Benign sebaceous neoplasm with lobules of sebocytes and mature sebaceous cells; multiple lesions may indicate Muir-Torre syndrome.
- Merkel cell carcinoma
- Neuroendocrine carcinoma with small blue cells, dotlike CK20, and CM2B4 positivity; it is aggressive and often associated with Merkel cell polyomavirus.
- Mycosis fungoides
- Cutaneous T-cell lymphoma with epidermotropic atypical lymphocytes, Pautrier microabscesses, and a CD4-positive T-cell phenotype with loss of CD7.
- Pautrier microabscess
- Intraepidermal cluster of atypical lymphocytes seen in mycosis fungoides; it is a helpful but not entirely specific diagnostic clue.
- Langerhans cell histiocytosis
- Proliferation of Langerhans cells with grooved nuclei, eosinophils, and positivity for S100, CD1a, and langerin; it can affect skin, bone, and other organs.
- Mastocytosis
- Dermal infiltrate of mast cells with tryptase and CD117 positivity; CD25 expression and urticaria pigmentosa are common, and systemic disease needs staging.
- Leukemia cutis
- Leukemic infiltrate in skin, often with a Grenz zone and perivascular or periadnexal distribution; immunohistochemistry helps classify myeloid or lymphoid lineage.
- Rosai-Dorfman disease
- Histiocytic proliferation with emperipolesis, S100 positivity, and CD1a negativity; it often presents with massive lymphadenopathy but can involve skin.
- Dermatofibroma
- Benign fibrous histiocytoma with collagen trapping, epidermal hyperplasia, factor XIIIa positivity, and CD34 negativity; it typically feels firm on palpation.
- Dermatofibrosarcoma protuberans
- Storiform spindle cell tumor with CD34 positivity and COL1A1-PDGFB fusion; it is locally aggressive and requires wide excision.
- Kaposi sarcoma
- Vascular tumor with slit-like spaces, spindle cells, and HHV8 positivity; it is associated with immunosuppression and presents as violaceous plaques or nodules.
- Infantile hemangioma
- Benign vascular tumor with GLUT1 positivity, distinguishing it from vascular malformations; it typically grows after birth and then involutes.
- Schwannoma
- Peripheral nerve sheath tumor with Antoni A and B areas, Verocay bodies, and S100 positivity; it is usually encapsulated and benign.
- Direct immunofluorescence
- Technique using labeled antibodies to detect immune deposits in skin; patterns help diagnose pemphigus, pemphigoid, dermatitis herpetiformis, and lupus.