在遗传决定的婴儿肌纤维素瘤中晚期复发. 一个案例报告和简要的重点关注复发情况
Alessio Conte1, Damiana De Padova2, Serena Giglio3
1Department of Neuroscience, Rehabilitation, Ophthalmology, Genetics, Maternal and Child Health, University of Genoa.
Journal of pediatric hematology/oncology
|August 14, 2024
概括
婴儿肌纤维素瘤 (IM) 是一种罕见的瘤疾病. 对PDGFRB变异的基因测试对于管理复发性IM病例和指导个性化治疗至关重要.
科学领域:
- 在瘤学瘤学.
- 遗传学 是一个遗传学.
- 儿科 儿科 儿科
背景情况:
- 婴儿肌纤维素瘤 (IM) 是一种罕见的良性瘤疾病,影响皮肤,皮下组织,肌肉,有时是内脏.
- 遗传形式的IM与PDGFRB或NOTCH3基因的变异有关.
- 目前的治疗方法包括保守的管理,手术和联合治疗方案,用于传播疾病.
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