UVL,particularly the ultraviolet B spectrum (290–320 nm) that induces mutations in tumor suppressor genes. UVB radiation damages DNA and affects the immune system resulting in a progressive genetic alterations and neoplasms. Nodular Basal Cell Carcinoma Papule or nodule, translucent or “pearly.” Skin- colored or reddish, smooth surface with telangiectasia.Portions of nodular BCC may have erosions or stipples of melanin pigmentation Ulcerating Basal Cell Carcinoma Ulcer (often covered with a crust) with a rolled border (rodent ulcer), which again is translucent, pearly, smooth with telangiectasia. Sclerosing Basal Cell Carcinoma Appears as a small patch of morphea or a superficial scar, often ill defined, skin-colored, whitish but also with peppery pigmentation. Superficial Basal Cell Carcinoma Appear as thin plaques .Pink or red characteristic fine thread like border and telangiectasia can be seen with the aid of a hand lens.This can also give rise to nodular and ulcerating BCC. BCC often bleeds with minimal excoriation. Solar keratosis, in comparison, does not bleed but is painful with excoriation. Pigmented Basal Cell Carcinoma May be brown to blue or black. Smooth, glistening surface hard, firm may be indistinguishable from superficial spreading or nodular melanoma but is usually harder. Cystic lesions may occur: round, oval shape, depressed center (“umbilicated”). Stippled pigmentation can be seen in any of BCC types. Cystic Basal Cell Carcinoma These dome shaped, blue – gray cystic nodules, are clinically similar to eccrine and apocrine hidrocystomas. Diagnosis of BCC Diagnosis of BCC is accomplished by accurate interpretation of the skin biopsy results. The preferred biopsy methods are shave biopsy, which is often sufficient, and punch biopsy Histopathology The malignant basal cells have large nuclei and relatively little cytoplasm. Although the nuclei are large, they may not appear atypical. Usually, mitotic figures are absent. Frequently, slit-like retraction of stroma from tumor islands is present, creating peritumoral lacunae that are helpful in histopathologic diagnosis. Differential Diagnosis Of BCC Squamous Cell Carcinoma Squamous cell carcinomas (SCCs) are malignant neoplasms derived from suprabasal epidermal keratinocytes. A firm, flesh- colored or erythematous, keratotic papule or plaque is most common, but SCCs may also be pigmented. Other presentations include as an ulcer, a smooth nodule , or a thick cutaneous horn. SCC may also be verrucous or present as an abscess. Nodular Melanoma Nodular melanoma (NM) is the second most common melanoma. It is more common for NM to begin de novo than to arise in a preexisting nevus. NM typically appears as a uniformly dark blue-black or bluish-red raised lesion, but 5% are amelanotic. Early lesions often lack asymmetry, have regular borders, and are a uniform color Bowen’s Disease (BD) Bowen disease (BD) is SCC in situ, it affects both skin and mucous membranes and has the potential to progress to invasive SCC. BD typically presents as a discrete, slowly enlarging, pink to erythematous thin plaque with well-demarcated, irregular borders and overlying scale or crust resembling a psoriatic plaque. Morphea Morphea is a chronic autoimmune disease characterized by sclerosis of the skin. Erythematous patch or thin plaque, Central sclerosis and violaceous, hyperpigmented border, Atrophy dermal, subcutaneous, or muscle Prognosis With appropriate treatment, the prognosis for most patients with BCC is excellent. Control rates as high as 99% have been achieved by MMS. For the rare patient with metastatic disease, prognosis is poor, with a mean survival of 8–10 months from the time of diagnosis.