Squamous Cell Carcinoma (SCC)
Info & Pathophysiology

Malignancy (>2cm dia) originating from proliferating keratinocytes in stratum spinosum. Less common, but more likely to metastasize than basal cell carcinoma (BCC).
Risk Factors: chronically damaged skin (e.g. inflammation, burns, ulcers), UV exposure, arsenic ingestion, immunosuppression
Clinical Diagnosis (Cutaneous subtype originating from actinic keratoses): crusty, scaly, raised, erythema around scales
Subtypes/Other Manifestations:
- SCC in situ (Bowen’s): does not invade past basement membrane, limited to epidermis
- Can be firm keratotic papules/plaques/nodules (more differentiated) or granulomas/ulcerative/necrotic tissue (poorly differentiated)
- Cutaneous horn: big wart projection
Pathophysiology: genetic dysregulation and mutation of TP53
Histological Characteristics
Presence of Keratin Pearl in dermis (concentric layers with thickening of epidermis), highly eosinophilic
Acanthosis (epidermal thickening)
Dyskeratotic cells

Treatment
Since higher risk of metastasis, first line treatment for cutaneous SCC is surgery (except SCC in situ)
Low Risk (<2cm, ≤ 6mm invasion beyond subcutaneous fat) treatment: standard surgical excision
- Standard Surgical Excision: vertical slide cuts in elliptical-shaped incision; margin examined post-op
High Risk: Mohs micrographic surgery
- Mohs: oblique excision, horizontal slices of cuts until no cancerous tissue detected; margins examined during surgery
SCC in situ treatment: curettage/excision, photodynamic therapy (use biological activator cream over lesion with light/radiation treatment), topical fluorouracil or imiquimod


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