拉布多米索尔科马的螺旋细胞变体:口腔腔腔的侵略性临床病例
Mayadevi Poojari1, Irappa Madabhavi2,3,4
1Department of Radiation Oncology, Oncolife Cancer Centre, Talegaon Dabhade, Pune, Maharashtra, India.
South Asian journal of cancer
|December 31, 2025
概括
螺旋细胞/硬化性狂宫肌肉瘤 (S-ScRMS) 是一个独特的实体. 这一案例凸显了它在儿童中的侵略性,对化疗和辐射有抗性,需要支持性护理.
科学领域:
- 在瘤学瘤学.
- 儿科瘤学 儿科瘤学
- 软组织肉瘤 (软组织肉瘤)
背景情况:
- 狂肌肉瘤 (RMS) 是一种恶性软组织瘤.
- 状细胞/硬化RMS (S-ScRMS) 在2013年被认定为一个独立的实体.
- S-ScRMS可能呈现出积极的临床过程,特别是在头部和部区域,局部复发率高,存活率降低.
研究的目的:
- 为了突出S-ScRMS的攻击性临床过程.
- 介绍一个患有S-ScRMS的儿科患者的案例研究.
主要方法:
- 一个患有S-ScRMS的7岁男孩的案例介绍.
- 审查患者的临床表现,诊断和治疗反应.
主要成果:
- 患者在15-20天的病史中出现左脸胀和疼痛.
- 诊断结果被证实为S-ScRMS.
- 尽管接受了化疗和放射治疗,但该疾病呈现出积极的进展,使其无法进行手术.
结论:
- 在儿科患者中,S-ScRMS可以表现出高度侵略性的临床行为.
- 在S-ScRMS中,治疗耐药性带来了重大挑战.
- 支持性护理可能是先进的,不可操作的S-ScRMS的唯一选择.
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