“…Although the majority of patients with cSCC present an excellent prognosis after adequate surgical resection, a subset of patients carry an increased risk of lymph node metastasis, local recurrence, and disease-specific death [ 7 , 9 , 14 ]. High-risk features include tumor diameter ≥ 2 cm, tumor thickness ≥ 2 mm, anatomic tumor site (face, ear, pre/post auricular area, genitalia, hands, and feet), poor histological differentiation, certain histological subtypes, evidence of perineural invasion, immunosuppression, and the presence of parotid metastases [ 3 , 7 , 16 ].…”