缬沙坦(或/和亚硝胺)诱导BCC和发育不良痣:当前的见解

G. Tchernev, N. Oliveira, Lorraine Joseph Kandathil, James W Patterson
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引用次数: 3

摘要

导语:治疗高血压的药物(沙坦类药物/血管紧张素受体阻滞剂)在生产过程中被亚硝胺污染,已被证明是一个严重的国际健康问题。造成这一问题的原因是,迄今为止发现的4种亚硝胺与皮肤肿瘤以及其他器官系统的肿瘤的同时或逐渐发展有关。血管紧张素受体在黑色素细胞和角化细胞肿瘤及其转移瘤中的存在增加了试图确定这两种成分(即亚硝胺和血管紧张素受体)在癌变过程中的相对重要性的困难。病例报告:我们报告一名40岁的动脉高血压患者,皮肤症状持续约7个月,临床表现为1)左眼内侧角附近出现一个孤立的肿瘤,组织学证实为基底细胞癌(BCC), 2)后汗沟区域多发,爆发性发育不良痣。患者的全身药物包括:比索洛尔5mg(1-0-1/2)和吲达帕胺1.5mg(1-0- 0),服用1年,用氨氯地平/缬沙坦5mg / 160 mg(1-0-1/2)治疗2年,初始治疗1年,随后减少剂量(1/2-0-0)再治疗1年。结论:我们报告了在使用含有缬沙坦的制剂后基底细胞癌和发育不良痣的同时发展。我们讨论了1)亚硝胺在发育不良痣和BCC发展中的可能主要因素的作用;2)沙坦类药物本身对皮肤血管紧张素受体的可能影响;3)低温免疫治疗药物性BCC的创新方案。关键词亚硝胺;缬沙坦;血管紧张素受体阻滞剂;动脉高血压;黑色素瘤;BCC;Cryoimmunotherapy
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Valsartan (or/and Nitrosamine) Induced BCC and Dysplastic Nevi: Current Insights
Introduction: Contamination of drugs for high blood pressure (sartans/ angiotensin receptor blockers) with nitrosamines occurs during the manufacturing process and has proven to be a serious international health problem. The reason for this problem is that the 4 nitrosamines discovered so far have been associated with the simultaneous or gradual development of cutaneous tumors as well as tumors of other organ systems. The presence of angiotensin receptors in melanocytic and keratinocytic tumors and their metastases adds difficulty when attempting to determine the relative importance of each of these two components (i.e. nitrosamines and angiotensin receptors) in the context of carcinogenesis. Case report: We report a 40-year-old patient with arterial hypertension with a duration of skin complaints of about 7 months, clinically manifested by 1) the appearance of a solitary tumor near the medial corner of the left eye, verified histologically as Basal Cell Carcinoma (BCC), and 2) multiple, eruptive dysplastic nevi in the area of the posterior sweat gutter. The patient’s systemic medications included: bisoprolol 5mg (1-0-1 / 2) and indapamide 1.5mg (1-0- 0), taken for one year, and 2 years of treatment with amlodipine / valsartan - 5 mg / 160 mg (1-0-1/2) for an initial period of 1 year, followed by a reduced dose of (1/2-0-0) for an additional year. Conclusion: We report the simultaneous development of basal cell carcinoma and dysplastic nevi after the use of a preparation containing generic valsartan. We discuss 1) the role of nitrosamines as possible major factors in the development of dysplastic nevi and BCC; 2) the possible effect of sartans themselves on angiotensin receptors in the skin and: 3) a new, innovative scheme for treatment of drug-induced BCC by cryoimmunotherapy. Keywords Nitrosamines; Valsartan; Angiotensin Receptor Blockers; Arterial Hypertension; Melanoma; BCC; Cryoimmunotherapy
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