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着色性干皮病变异型(XP-V)中的癌症防护。

Cancer protection in xeroderma pigmentosum variant (XP-V).

作者信息

Somos S, Farkas B, Schneider I

机构信息

Department of Dermatology, Medical University of Pécs, Hungary.

出版信息

Anticancer Res. 1999 May-Jun;19(3B):2195-9.

Abstract

We describe herein a brother and sister diagnosed with xeroderma pigmentosum variant (XP-V) in early adult life, who presented with increased sensitivity to sunlight and with cutaneous carcinomas on sun-damaged skin. The 27-year-old male farmer (Case 1.) was diagnosed with advanced squamous cell carcinoma (SCC) and multiple actinic lesions. Surgical removal of these lesions was performed. Three months later he died of multiple pelvic metastases of SCC. His 29-year-old sister (Case 2.) was operated on for different tumors, histologically SCC-s or basal cell carcinomas (BCC), or praecancerous conditions many times. After a two year interval she was treated with low dose isotretinoin (2 mg/body weight). Diagnosis of XP-V was based on unscheduled DNA analysis (USD) and on clinical symptoms. We observed that during the long lasting isotretinoin treatment the tumor frequency dropped to a quarter. Therefore, the isotretinoin treatment seems to be a good approach for cancer prevention in conditions with high predisposition to skin cancer, such as in XP-V.

摘要

我们在此描述一对兄妹,他们在成年早期被诊断为着色性干皮病变异型(XP-V),表现出对阳光的敏感性增加以及在受阳光损伤的皮肤上出现皮肤癌。这位27岁的男性农民(病例1)被诊断为晚期鳞状细胞癌(SCC)和多处光化性病变。对这些病变进行了手术切除。三个月后,他死于SCC的多处盆腔转移。他29岁的妹妹(病例2)因不同肿瘤多次接受手术,组织学上为SCC或基底细胞癌(BCC),或癌前病变。两年后,她接受了低剂量异维A酸(2mg/体重)治疗。XP-V的诊断基于非计划DNA分析(USD)和临床症状。我们观察到,在长期的异维A酸治疗期间,肿瘤发生率降至四分之一。因此,对于像XP-V这种皮肤癌易感性高的情况,异维A酸治疗似乎是预防癌症的一种好方法。

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