Sclerodermiform basal cell carcinoma: rare form in a young patient

I. Assenhaji, M. Bennani, J. Ziani, S. Elloudi, H. Baybay, F. Mernissi
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Abstract

We report the cases of one 34-year-old, phototype 3, the delay of consultation was 4 years, and the factors risk was mainly sun exposure, the symptoms leading to consultation were ulceration. The clinical examination found sclerodermiform plaque, poorly limited, and erosion at the forehead. The dermoscopy revealed telangiectasia and vascularization in tree trunks, as well as ulceration. The rest of the somatic examination was normal. The diagnosis of basal cell carcinoma scleroderma was confirmed by histology. Surgical excision with margins was performed (Figure 1 & 2).
硬皮样基底细胞癌:罕见的年轻患者
我们报告1例34岁,3型,延迟问诊4年,危险因素主要为日晒,导致问诊的症状为溃疡。临床检查发现硬皮样斑块,局限性差,额头糜烂。皮肤镜检查显示树干毛细血管扩张和血管化,以及溃疡。其余躯体检查均正常。病理证实为基底细胞癌硬皮病。行带边缘的手术切除(图1和2)。
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