Eugene D W, Joshi K D
Plastic and Burn and Reconstructive Unit, Kathmandu Medical College, Sinamangal, Kathmandu, Nepal.
Kathmandu Univ Med J (KUMJ). 2006 Jan-Mar;4(1):78-81.
Xeroderma pigmentosa is a rare inherited autosomal recessive disease with the inability to repair DNA damage caused by UV light. Recognized in the late 1800 by Maritz Kaposi it has been reported world wide and in all races with an over prevalence of 1-4 per million population. Kunwar et al. Those affected are extremely sensitive to the UV portion of the light and have a 2000-fold increased risk of skin cancer in the sun exposed skin. Basal cell carcinoma is the most commonly associated carcinoma followed by Squamous cell carcinoma and Melanoma. The pigmentation on the face and the rest of the body can be horribly disfiguring. The recurring cancer occurring on the face and repeated surgical treatment for the ulcerations have important social and psychological implications not encountered with other cancers. We report two cases of BCC and melanoma. The first case is of BCC of the face in a teenaged girl coexisting with xeroderma pigmentosa. The second case presented with melanoma of the scalp in a 10 year old female child. The details of these cases are presented and the management.
着色性干皮病是一种罕见的常染色体隐性遗传性疾病,无法修复紫外线引起的DNA损伤。19世纪末由马里茨·卡波西首次发现,全世界所有种族均有报道,发病率约为百万分之一至百万分之四。昆瓦尔等人指出,患者对光线中的紫外线极其敏感,在暴露于阳光下的皮肤中患皮肤癌的风险增加2000倍。最常见的相关癌症是基底细胞癌,其次是鳞状细胞癌和黑色素瘤。面部和身体其他部位的色素沉着会严重毁容。面部反复出现的癌症以及针对溃疡的反复手术治疗具有重要的社会和心理影响,这是其他癌症所没有的。我们报告了两例基底细胞癌和黑色素瘤病例。第一例是一名患有着色性干皮病的青少年女孩面部的基底细胞癌。第二例是一名10岁女童头皮的黑色素瘤。本文介绍了这些病例的详细情况及治疗方法。