带有新型MN1::TAF3融合的螺旋细胞瘤:一个幼儿的罕见病例
Jesse White1, Kerri Becktell2, Amanda Hopp3
1Medical College of Wisconsin Affiliated Hospitals.
Journal of pediatric hematology/oncology
|October 8, 2024
概括
儿科轨道脊柱细胞瘤是罕见的. 在一个18个月大的婴儿身上发现了一种新的MN1::TAF3基因融合,这给诊断和治疗带来了挑战.
科学领域:
- 儿科瘤学 儿科瘤学
- 分子病理学分子病理学
- 眼科医生 眼科 眼科
背景情况:
- 脊柱细胞瘤在儿童中很少被记录.
- 儿科患者的轨道瘤需要仔细的诊断和管理.
- 单边死可能是轨道病理的初始迹象.
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