1型神经纤维素瘤 mozaicism 在宪法不匹配修复缺陷的患者
Léa Guerrini-Rousseau1,2, Eric Pasmant3,4, Martine Muleris5,6
1Department of Pediatric and Adolescent Oncology, Gustave Roussy Cancer Campus, Université Paris-Saclay, Villejuif, France lea.guerrini-rousseau@gustaveroussy.fr.
区分构造不匹配修复缺陷 (CMMRD) 和神经纤维素瘤类型1 (NF1) 是至关重要的. 这一案例突出显示CMMRD与马赛克NF1,表明NF1通路参与CMMRD相关的结质瘤和潜在的MEK抑制剂使用.
科学领域:
- 在瘤学瘤学.
- 遗传学 遗传学 是一个
- 儿科瘤学 儿科瘤学
背景情况:
- 由于不同的管理策略,准确诊断构造不匹配修复缺陷 (CMMRD) 和神经纤维素瘤类型1 (NF1) 之间至关重要.
- 两种CMMRD和NF1都是罕见的遗传疾病,可以呈现重叠的临床特征,使差异诊断复杂化.
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