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着色性干皮病是一种隐性遗传性皮肤病,属癌前病变之一,易合并皮肤癌,目前尚无有效的治疗方法。我们采用面部换皮法,即面部皮肤切除移植全厚皮片的方法治疗着色性干皮病合并面部多发性皮肤癌,效果满意,报告如下。病例介绍例1.男,4岁。1977年12月2日初诊。主诉:出生后6个月面部出现黑色素斑,逐渐增多并波及全身,以裸露部位为著,日晒后加重。3个月前鼻根部出现一肿物,逐渐增大。病儿之父母非近亲婚配,家庭中无类似病症。体检:全身皮肤发暗,且有大小不等的密集黑斑,皮肤发干粗糙。病损以面、颈及手
Xeroderma pigmentosum is a recessive hereditary skin disease. It is one of the precancerous lesions. It is easy to merge skin cancer. There is no effective treatment. We used the facial skin grafting method, that is, facial skin grafting and full thickness skin grafting for the treatment of xeroderma pigmentosum combined with multiple facial skin cancers. The results were satisfactory. The report is as follows. Case Introduction 1. Male, 4 years old. Newly diagnosed on December 2, 1977. Chief complaint: Facial speckles appeared 6 months after birth, gradually increased and spread throughout the body, and exposed to the exposed parts, which increased after sun exposure. A tumor appeared in the root of the nose 3 months earlier and gradually increased. Parents of sick children are not close relatives, and there are no similar illnesses in the family. Physical examination: The skin of the body is dark, and there are dense dark spots of varying sizes. The skin is dry and rough. Lesions to face, neck and hand