患有皮肤颜色的儿科患者的瘤性基因皮肤病:一篇综述
Sherwin Fazelpour1, Sandhya C Deverapalli2, Bichchau Nguyen2
1St Joseph's Medical Center, Stockton, CA, USA.
Clinical and experimental dermatology
|August 3, 2024
概括
患有基因皮肤病的儿童患皮肤癌的风险更高. 这项研究强调了皮肤颜色的儿童表现和结果的差异,强调了在儿科瘤学中识别非经典征兆的必要性.
科学领域:
- 儿科皮肤病学 儿科皮肤病学
- 在瘤学瘤学.
- 遗传学 是一个遗传学.
背景情况:
- 皮肤瘤在儿童中很少见,通常与紫外线辐射等环境因素有关.
- 某些基因皮肤病显著增加了儿科恶性瘤的风险,需要保持警的监测.
- 现有的数据主要反映了白人患者,肤色有色人群的代表性不足.
研究的目的:
- 为了阐明皮肤颜色的儿科患者的基因皮肤病的皮肤表现.
- 为了识别和比较皮肤颜色和白人儿童之间基因皮肤病的表现的相对差异.
- 强调识别非古典标志对于公平的患者管理的重要性.
主要方法:
- 从236篇发表的文章中对504名儿科患者 (≤17岁) 的系统文献综述.
- 包括专注于基因皮肤病和皮肤瘤的病例报告.
- 对临床表现的分析,重点关注有色人群皮肤的差异.
主要成果:
- 皮肤有色的患者表现出与基因皮肤病相关的经典发现较少.
- 在皮肤有色的儿科患者中观察到痕和色素失调的更高发病率.
- 在受影响的肤色有色人群中,血缘关系的患病率更高.
结论:
- 在皮肤有色的儿科患者中识别基因皮肤病的非经典症状对于准确诊断至关重要.
- 鉴于这些差异,定制的管理策略可以改善代表性不足的人群的结果.
- 需要进一步的研究,以确保在不同种族的儿科皮肤瘤学中提供公平的护理和结果.
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