内心外巴肺封存:一个案例报告和对独特胚胎变异的系统审查
Margherita Roveri1,2, Giada Pedroni1,2, Alessandra Preziosi1
1Pediatric Surgery, ASST Grande Ospedale Metropolitano Niguarda, 20162 Milan, Italy.
Journal of clinical medicine
|February 13, 2026
概括
心脏内外肺部封存 (ELPS) 是一种罕见的先天性异常. 早期诊断和手术切除对于预防严重并发症至关重要,如心脏坦波纳德.
科学领域:
- 遗传性缺陷 遗传性缺陷是一种先天性缺陷
- 胸部外科手术 胸部外科手术
- 儿童心脏病学 儿童心脏病学
背景情况:
- 心脏内外肺部封存 (ELPS) 是一种极其罕见的先天性形.
- 它的位置可以模仿瘤,呈现诊断和手术困难.
- 本研究提出了一个新的案例和一个系统的文献综述.
研究的目的:
- 为了描述一个心脏内皮层ELPS病例.
- 系统地审查关于心内皮质ELPS的文献.
- 为突出这一罕见疾病的诊断和手术考虑.
主要方法:
- 通过使用PRISMA指南进行了系统的文献审查.
- 搜索的数据库包括 PubMed,Scopus 和 Embase.
- 纳入标准是经组织学证实的腹膜内心ELPS.
主要成果:
- 已经报告了11例心内皮质ELPS病例,包括目前的病例.
- 产前检测发生在54%的病例中;两个病例导致胎儿死于心脏吸管.
- 来自肺动脉的异常动脉供应 (54%) 和向右前庭/上 vena cava (45%) 的静脉排水是常见的发现.
结论:
- 腹腔内心ELPS是一种罕见但可以通过手术治疗的疾病.
- 早期识别和彻底切除对于避免危及生命的并发症至关重要.
- 一致的血管模式表明ELPS是CPAM-分离谱中独特的胚胎变异.
关键词:
生产性肺部形 产生的肺部形这是一种先天性瘤 (congenital teratoma).混合损伤 混合损伤 混合损伤肺内内心外肺部封存 内心外肺部封存腹膜内心病变是心脏内部的病变.儿科胸部手术 儿科胸部手术更多相关视频
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