Head and Neck Cutaneous Squamous Cell Carcinoma Differential Diagnoses
- Author: Marcus Monroe, MD; Chief Editor: Arlen D Meyers, MD, MBA more...
Diagnostic Considerations
The key diagnostic consideration is that early detection and treatment by multiple modalities is important for better prognosis in head and neck cancer. A complete head and neck examination with indirect nasopharyngeal and laryngopharyngeal mirror examination is mandatory.
Keep in mind that although the typical patient with squamous cell carcinoma (SCC) is of northern European descent and presents with a family history of skin cancer, a personal history of previous skin cancer, and/or an extensive history of sun exposure, a detailed history and physical examination is crucial (see Clinical Presentation),and the clinician should be aware of the risk factors for high-risk disease (see Prognosis).Cutaneous SCCs can be experimentally produced with ultraviolet (UV) light exposure, almost to the exclusion of other types of cancer. Marjolin ulcer appears as a new area of induration, elevation, or ulceration at the site of a preexisting scar or ulcer. The diagnosis of Marjolin ulcer should be considered in any ulcer that fails to heal with standard therapy.
Pseudoepitheliomatous hyperplasia (PEH) is a histologic finding found in keratoacanthoma and SCC and in certain other reactions such as tattoo reactions; this is important to remember when presented with the diagnosis of an SCC arising in a tattoo. That is, the clinician must ensure that the PEH is associated with cancer. PEH can also be present in lesions of hypertropic lupus. When lesions with PEH are found in patients with a history of lupus, the clinician must differentiate between lesions that are definitely SCC and lesions of hypertropic lupus that are mimicking SCC or keratoacanthoma.
Other Conditions to Be Considered
The following conditions should also be considered when evaluating a patient with suspected SCC:
- Cancerous lesions - Sebaceous cell carcinoma and rhabdomyosarcoma
- Congenital tumors - Dermoids, dermolipomas, and episcleral osseous choristoma
- Conjunctival degeneration - Pinguecula and amyloidosis
- Hereditary lesions - Benign hereditary intraepithelial dyskeratosis
- Lymphoid tumors - Lymphoid neoplasia, benign reactive lymphoid hyperplasia, and leukemic infiltrates
- Neuroectodermal tumors - Nevus, primary acquired melanosis, and melanoma
- Papillomas – Human papillomavirus (HPV)-induced papillomas
- Pseudocancerous lesions - Pseudoepitheliomatous hyperplasia and keratoacanthoma
- Vascular lesions - Angioma, lymphangioma, Kaposi sarcoma, and pyogenic granuloma
- Xanthomatous lesions -Juvenile xanthogranuloma and fibrous xanthoma
Differential Diagnoses
- Actinic Keratosis
- Atopic Dermatitis
- Atypical Fibroxanthoma
- Basal Cell Carcinoma
- Benign Skin Lesions
- Bowenoid Papulosis
- Chemical Burns
- Contact Dermatitis
- Limbal Dermoid
- Pyoderma Gangrenosum
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- Table 1. Estimated Number of New Cancer Cases and Deaths in Both Sexes in the United States in 2004
- Table 2. TNM Stage Grouping
- Table 3. Histologic and Clinical Features of Squamous Cell Carcinoma (SCC) Variants
- Table 4. Summary of Characteristics of Papillary Epithelial Lesions and Verrucous Carcinoma
| Cancer | New Cases | Deaths |
| Oral cavity and pharynx | 28,260 | 7230 |
| Tongue | 7320 | 1700 |
| Mouth | 10,080 | 1890 |
| Pharynx | 8250 | 2070 |
| Other oral cavity | 2160 | 1570 |
| Larynx | 10,270 | 3830 |
| Source: American Cancer Society, 2004.[46] Note: The US Census Bureau estimated that the US population was approximately 282,000,000. | ||
| Stage | Primary Tumor | Regional Lymph Nodes | Distant Metastasis |
| Stage 0 | Tis | N0 | M0 |
| Stage I | T1 | N0 | M0 |
| Stage II | T2 | N0 | M0 |
| Stage III | T3 | N0 | M0 |
| T1, T2, T3 | N1 | M0 | |
| Stage IV | T4 | N0, N1 | M0 |
| Any T | N2, N3 | M0 | |
| Any T | Any N | M1 |
| Tumor | Histologic Characteristics | Clinical Characteristics |
| Keratoacanthoma | Keratin-filled crater Well-differentiated (mild atypia) Neutrophil microabscesses Eosinophils in dermal infiltrate Elastic tissue trapping Lack of acantholysis | Solitary nodule Central craterlike depression Rapid growth May spontaneously involute |
| Spindle cell carcinoma | Atypical spindle cells Foci of squamous differentiation May resemble other spindle cell tumors (eg, atypical fibroxanthoma) | Resembles typical SCC May be clinically aggressive |
| Acantholytic (adenoid) SCC | Glandlike differentiation Acantholysis May resemble adenocarcinoma or sweat gland carcinoma | Arises on sun-damaged skin Elderly patients Resembles typical SCC Clinically aggressive |
| Verrucous carcinoma | Well-differentiated (glassy atypia) Surface resembles verruca Bulbous downward proliferation "Bulldozing" invasion | Oral, genital, or plantar foot Indolent growth Locally destructive Rarely metastasizes |
| Sarcomatoid SCC | Poorly differentiated cells resembling sarcoma | Clinical appearance may be that of typical SCC or may have more nodular appearance with less surface change Elevated risk of local recurrence and metastasis |
| Tumor | Epithelium | Invasion and Inflammation |
| Benign squamous papilloma | Minimal to no epithelial atypia without any stromal invasion | No inflammation in stroma; no epithelial cells, nests, or broad fronts in stroma |
| Papillary SCCIS | Full-thickness epithelial atypia without invasion | No invasive epithelial component in stroma; minimal inflammatory reaction |
| Papillary SCC, invasive | Epithelial atypia, which may or may not be full thickness, overlying stromal invasion; invasion occurs by means of elongated, stabbing fronts, small nests or individual cells | Pointed, narrow epithelium extending into stroma, with epithelial nests and/or individual cells surrounded by inflammatory cells, which may be eosinophils, neutrophils, macrophages, plasma cells, and/or lymphocytes in any combination |
| Verrucous carcinoma | Bland, highly keratinized, squamous epithelium, with invasion in broad, rounded, pushing fronts | No individual cells or squamous nests in stroma; advanced portion of the epithelial pushing front surrounded by tightly hugging infiltrate of mononuclear inflammatory cells |

