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Dermatofibrosarcoma protuberans in a young patient with epidermolysis bullosa: a case report

机译:Dermatofibrosarcoma protuberans在一名年轻患者有表皮术博览会的患者:案例报告

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Epidermolysis bullosa is a group of rare inherited skin diseases characterized by blister formation following mechanical skin trauma. Epidermolysis bullosa is associated with increased skin cancer rates, predominantly squamous cell carcinomas, yet to our best knowledge, there is no reported case of dermatofibrosarcoma protuberans in a patient with Epidermolysis bullosa. Here, we present a 26-year-old man with junctional epidermolysis bullosa, who developed a DFSP on the neck. Initial, the skin alteration was mistakenly not considered malignant, which resulted in inadequate safety margins. The complete resection required a local flap to close the defect, which is not unproblematic because of the chronic inflammation and impaired healing potential of the skin due to Epidermolysis bullosa. To our best knowledge, this is the first reported case of a skin-associated sarcoma in a patient with EB; however, further investigation is required to verify a correlation.
机译:结果表皮溶解Bullosa是一种稀有的遗传性皮肤病,其特征在于机械皮肤创伤后泡罩形成。 结果表皮溶解性患者癌症率增加,主要是鳞状细胞癌,尚未达到我们最佳知识,患有表皮神经分解Bullosa的患者中没有报告的皮肤病病例。 在这里,我们展示了一名26岁的男子,伴随着颈颈部的交叉表皮溶解Bullosa。 首先,皮肤改变被误认为是恶性的恶性,这导致安全利润率不足。 完全切除需要局部襟翼以关闭缺陷,这不是由于表皮细胞表皮细胞引起的慢性炎症和皮肤的愈合潜力受损的缺陷。 为了我们的最佳知识,这是第一个据报道的患者在eB的患者中举报的案例; 但是,需要进一步调查来验证相关性。

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