在儿科患者的腹腔内肌肉肉瘤呈现为急性尾炎的儿科患者
M C Moolamannil1, H Khan1, S Karim1
1Bedfordshire Hospitals NHS Foundation Trust, UK.
Annals of the Royal College of Surgeons of England
|July 31, 2024
概括
我们报告了一例罕见的胚胎性狂宫肌肉瘤 (RMS) 病例,该病例发生在患有急性腹部症状的儿童身上. 发现瘤是前腹壁上的出血性死体质量.
科学领域:
- 在瘤学瘤学.
- 儿科病理学 儿科病理学
- 手术病理学手术病理学
背景情况:
- 狂肌肉瘤 (RMS) 是一种软组织肉瘤,其亚型包括胚胎性和膜性.
- 复发性肌痛综合症通常会影响四肢,头部/部或生殖泌尿系统.
- 腹壁RMS很少见,通常由于质量效应而迟迟出现.
研究的目的:
- 在孩子身上呈现一种罕见的胚胎RMS病例.
- 为了突出RMS在前腹壁的不寻常呈现.
- 讨论这种罕见表现的诊断和临床影响.
主要方法:
- 一个儿科病人的病例报告.
- 在手术内发现出血性死体质量.
- 胚胎性拉布多米索尔科马的组织病理学确认.
主要成果:
- 一个孩子出现了急性腹部症状.
- 在手术期间,在前腹壁上发现了出血的死体质量.
- 组织学证实了这种质量是胚胎性狂宫肌肉瘤.
结论:
- 胚胎性狂宫肌肉瘤可以不典型地出现在前腹壁.
- 急性腹部症状可能是罕见RMS位置的迹象.
- 早期诊断和手术干预对于罕见的儿科恶性瘤至关重要.
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