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圣囊多症:一个病例报告和文献综述
Shiyas Mohammedali1,2, Saif Badran3, Sohail J Quazi2
1Department of Pediatric Plastic Surgery, Sidra Medicine Hospital, Doha, Qatar.
JPRAS open
|March 9, 2026
概括
这份病例报告详细介绍了一种罕见的先天性疾病 - - 婴儿多肢症. 手术切除是成功的,强调多学科的护理,以获得最佳的结果.
科学领域:
- 医学遗传学 医学遗传学
- 儿科手术 儿科手术
- 发展生物学 发展生物学
背景情况:
- 多肢症是一种罕见的先天性异常,涉及超数的四肢.
- 它于1877年首次被描述,其病理生理学尚未完全理解.
- 圣囊细胞多重症带来了独特的外科手术挑战.
研究的目的:
- 在婴儿中报告一个神经囊多叶病例.
- 审查有关多菌病理生理学,表现和管理的文献.
- 强调多学科护理在手术治疗中的作用.
主要方法:
- 一个2个月大的婴儿患上神经囊多重症的案例介绍.
- 综合的文献综述关于多.
- 手术切除辅助肢体,同时保留周围的解剖结构.
主要成果:
- 成功的手术切除了辅助肢体.
- 良好的术后伤口愈合和美容结果.
- 精确的外科手术技术的可行性已被证明.
结论:
- 多学科的护理对于管理多重症至关重要.
- 仔细的手术前评估和精确的手术技术导致了有利的结果.
- 这个案例有助于理解和管理罕见的先天性四肢异常.
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