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Genetic study of familial uveal melanoma: association of uveal and cutaneous melanoma with cutaneous and ocular nevi.

机译:家族性葡萄膜黑色素瘤的遗传研究:葡萄膜和皮肤黑色素瘤与皮肤和眼痣的关系。

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PURPOSE: To evaluate a kindred with familial uveal and cutaneous melanoma and to identify potential genetic and environmental factors that may predispose individuals to develop uveal melanoma. DESIGN: Family-based case report with detailed clinical and genetic evaluation. PARTICIPANTS: Ten siblings in a single nuclear family. METHODS: Evaluation of a large sibship via family history, complete eye and skin examinations, environmental risk factor questionnaire, and genetic testing, as well as a MEDLINE search of familial uveal melanoma kindreds. MAIN OUTCOME MEASURES: Cutaneous and ocular nevi, benign and malignant neoplasms of skin and other sites, brief skin cancer risk assessment tool risk classification for cutaneous melanoma, DNA sequencing of p16INK4a and p14ARF genes, and citations on familial uveal melanoma. RESULTS: The proband and his mother had uveal melanoma, 3 cutaneous melanomas occurred among 2 siblings, and 2 other siblings had basal cell carcinomas. No germline mutations were detected inthe melanoma-associated tumor suppressor genes p16INK4a and p14ARF. Seven out of 10 siblings had a history of cutaneous and/or ocular nevi. Of the 3 subjects without nevi, 2 had histories of eye or skin malignancies (1 uveal melanoma, 1 basal cell carcinoma). Three of the 10 siblings had relevant ocular findings (2 choroidal nevi, 1 uveal melanoma). Six were also found to be in the "high-risk" classification for cutaneous malignancies based on scores from a previously validated risk assessment tool. This family, combined with the 91 previously reported familial uveal melanoma kindreds, brings to 92 the total number thus far recorded. CONCLUSIONS: Our results strengthen the association between uveal melanoma, atypical nevi, and cutaneous melanoma. This relationship supports the recommendation that individuals with a personal or family history of uveal melanoma, particularly in combination with atypical nevi, should be regularly screened for uveal and cutaneous melanoma.
机译:目的:评估家族性葡萄膜和皮肤黑色素瘤的亲缘关系,并确定可能导致个体发展葡萄膜黑色素瘤的潜在遗传和环境因素。设计:基于家庭的病例报告,具有详细的临床和遗传评估。参加者:一个核心家庭中有10个兄弟姐妹。方法:通过家族病史,完整的眼睛和皮肤检查,环境危险因素问卷调查表以及基因检测,以及通过MEDLINE搜索家族性葡萄膜黑色素瘤亲属来评估大同胞关系。主要观察指标:皮肤和眼痣,皮肤和其他部位的良性和恶性肿瘤,皮肤黑色素瘤的简要皮肤癌风险评估工具风险分类,p16INK4a和p14ARF基因的DNA测序以及家族性葡萄膜黑色素瘤的引用。结果:先证者和他的母亲患有葡萄膜黑色素瘤,两个兄弟姐妹中发生了3例皮肤黑色素瘤,另外两个兄弟姐妹患有基底细胞癌。在黑素瘤相关的肿瘤抑制基因p16INK4a和p14ARF中未检测到种系突变。 10个兄弟姐妹中有7个有皮肤和/或眼痣病史。在没有痣的3名受试者中,有2名有眼或皮肤恶性肿瘤病史(1例葡萄膜黑色素瘤,1例基底细胞癌)。 10个兄弟姐妹中有3个具有相关的眼部检查结果(2个脉络膜痣,1个葡萄膜黑色素瘤)。根据先前验证的风险评估工具得出的分数,发现皮肤恶性肿瘤的“高风险”分类中也有6个。该家族与先前报道的91个家族性葡萄膜黑色素瘤家族相结合,迄今已记录的总数为92。结论:我们的结果加强了葡萄膜黑色素瘤,非典型痣和皮肤黑色素瘤之间的联系。这种关系支持以下建议:应定期筛查具有葡萄膜黑色素瘤的个人或家族病史的患者,尤其是与非典型痣结合的患者,尤其是葡萄膜黑色素瘤和皮肤黑色素瘤。

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