Malignant epithelial tumor of squamous keratinocytes
Etiology/Pathogenesis
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Most cases are related to UV radiation
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Previous radiation therapy implicated in some cases; usually associated with more aggressive SCC
Clinical Issues
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Often arises in sun-damaged skin of elderly patients (usually head and neck)
Vast majority of cases associated with preexisting actinic keratosis (AK)
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Complete surgical excision is optimal and definitive therapy
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Prognosis usually good in superficial and well-differentiated cases
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Worse prognosis with poorly differentiated, deeply invasive, or aggressive subtypes
Microscopic
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Proliferation of invasive atypical keratinocytes, often with areas of keratinization (keratin pearls) and squamous eddies
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Cells are present in nests, sheets, and cords
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Cytologically, cells show abundant eosinophilic cytoplasm and large nucleus with vesicular chromatin and prominent nucleoli
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Degree of differentiation is variable, ranging from well to moderately to poorly differentiated
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Multiple variants of differing malignant potential described
Top Differential Diagnoses
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Poorly differentiated carcinoma (Including metastatic)
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Pseudoepitheliomatous hyperplasia
TERMINOLOGY
Abbreviations
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Squamous cell carcinoma (SCC)
Synonyms
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Sarcomatoid carcinoma (spindle cell carcinoma/carcinosarcoma/metaplastic carcinoma)
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Acantholytic (adenoid/pseudoglandular) SCC
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Verrucous carcinoma: Well-differentiated variant
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Keratoacanthoma (KA): Very well-differentiated variant, regresses spontaneously
Definitions
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Malignant tumor of squamous keratinocytes
ETIOLOGY/PATHOGENESIS
Environmental Exposure
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Most cases are related to UV radiation
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Some cases are likely related to chronic inflammation (i.e., SCC arising in burns, lupus, lichen planus)
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Previous radiation therapy is implicated in some cases; usually associated with more aggressive SCC
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Chronic wounds and burn scars also can be associated with high-risk SCC
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Human papillomavirus is associated with some cases
Especially verrucous carcinoma (low grade) and SCC in immunosuppressed patients (high grade)
CLINICAL ISSUES
Epidemiology
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Age
Usually in elderly, especially solar-related lesions
However, can present in wide age range (34-95 years)
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Rare cases in children (should prompt genetic studies)
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Sex
Slightly more common in males, overall
Presentation
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Slow-growing papular, nodular, or plaque lesion
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Often arises in sun-damaged skin (head and neck tumors)
Vast majority of cases associated with preexisting actinic keratosis (AK)
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May be ulcerated or bleeding
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Ear canal and middle ear tumors may present with pain, hearing loss, and discharge
Treatment
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Surgical approaches
Complete surgical excision is optimal and definitive therapy
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Mohs surgery has been shown to be highly effective for most tumors
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Drugs
If patients are not surgical candidates, topical chemotherapeutics or immunomodulators may be used
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Radiation
May be used for very advanced cases where surgical therapy is not curative
Prognosis
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Usually excellent in most cases
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Worse prognosis with poorly differentiated, deeply invasive, or rare aggressive subtypes
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Site of tumor important for prognosis
Lip and ear tumors more aggressive, regardless of degree of differentiation
MACROSCOPIC
General Features
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Papular to nodular or plaque-like lesion; can be exophytic
May be ulcerated or hemorrhagic
Size
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Variable; can be small or large lesions
MICROSCOPIC
Histologic Features