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The prevalence rate of sporadic lesions is 2%8% in Caucasians, with a melanoma relative risk ranging from 1.6 (95% confidence interval [CI] 1.41.8) for subjects with one dysplastic nevus to 10.5 (95% CI 5.121.8) for subjects with five or more dysplastic nevi.(4) Familial-type dysplastic syndrome was classified by Kraemer as: Type B for individuals with a family history of dysplastic nevi

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Serious complications, including allergic reactions or infections if administered incorrectly, are rare

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Computed tomography (CT) demonstrated a large heterogeneous circumscribed mass in the left hepatic lobe and contrast enhancement in the arterial and portal phases (Figure 1A, B, C)

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doi: 10.6065/apem.2016.21.4.193

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