Grampurohit Vandana U, Dinesh U S, Rao Ravikala
Department of Pathology, SDM College of Medical Sciences and Hospital, Dharwad, Karnataka, India.
J Cancer Res Ther. 2011 Apr-Jun;7(2):205-7. doi: 10.4103/0973-1482.82932.
Xeroderma pigmentosum is a genodermatosis characterized by photosensitivity and the development of cutaneous and internal malignancies at an early age. The basic defect underlying the clinical manifestations is a nucleotide excision repair defect, leading to defective repair of DNA damaged by ultraviolet radiation. These patients exhibit enhanced sensitivity to ionizing radiation. Patients with xeroderma pigmentosum who are younger than 20 years of age have a greater than 1000-fold increased risk of developing skin cancer. Early detection of these malignancies is necessary because they are fast growing, metastasize early and lead to death. Although, early detection and treatment of cutaneous malignancies will reduce the morbidity and mortality, genetic counseling remains the most important measure for preventing xeroderma pigmentosum. We report a case of xeroderma pigmentosum in an 18-year-old male presenting with multiple cutaneous malignancies: squamous cell carcinoma, malignant melanoma and pigmented basal cell carcinoma.
着色性干皮病是一种遗传性皮肤病,其特征为光敏感以及在早年发生皮肤和内脏恶性肿瘤。临床表现背后的基本缺陷是核苷酸切除修复缺陷,导致由紫外线辐射损伤的DNA修复缺陷。这些患者对电离辐射表现出增强的敏感性。年龄小于20岁的着色性干皮病患者患皮肤癌的风险增加超过1000倍。早期发现这些恶性肿瘤很有必要,因为它们生长迅速、早期转移并导致死亡。尽管皮肤恶性肿瘤的早期发现和治疗将降低发病率和死亡率,但遗传咨询仍然是预防着色性干皮病的最重要措施。我们报告一例18岁男性着色性干皮病患者,其患有多种皮肤恶性肿瘤:鳞状细胞癌、恶性黑色素瘤和色素性基底细胞癌。