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一个患有血管埃勒斯-丹洛斯综合征的患者的鱼骨引起小肠穿孔:一个病例报告
Hiroki Nakahara1, Shunsuke Doi1, Satoshi Yasuda1
1Department of Surgery, Nara Medical University 840 Shijo-cho, Kashihara, Nara, Japan.
Journal of surgical case reports
|March 5, 2025
概括
本案例研究突出了一个罕见的胃肠道穿孔病例,该病例发生在一个由鱼骨引起的血管埃勒斯-丹洛斯综合征 (vEDS) 患者身上. 迅速的手术干预对于管理这种危及生命的并发症至关重要.
科学领域:
- 胃肠病学 胃肠病学
- 血管外科 血管外科
- 遗传学 遗传学 是一个
背景情况:
- 胃肠道 (GI) 穿孔在患有血管埃勒斯-丹洛斯综合征 (vEDS) 的患者中带来了重大管理挑战,这是一种与动脉脆弱性相关的遗传连接组织疾病.
- 外体摄入导致胃肠道穿孔是不常见的,并且它在vEDS患者的发生是非常罕见的,需要高度的怀疑指数和量身定制的临床方法.
研究的目的:
- 报告一个独特的细肠穿孔病例,归因于一个被诊断患有血管埃勒斯-丹洛斯综合征的患者的鱼骨.
- 强调对个性化手术策略和精细的术后护理的关键需求,以管理这种罕见的胃肠道并发症.
主要方法:
- 进行了全面的临床评估,包括详细的病史和计算机断层扫描 (CT) 成像,以诊断肠道穿孔的原因和程度.
- 为了进行外科探索和干预,进行了紧急腹腔切除,涉及切除含有鱼骨异物体的受影响小肠段.
主要成果:
- 一个鱼骨被确定为vEDS的男性患者的阴茎穿孔和介质透的致病原体.
- 患者经历了成功的小肠切除并康复,尽管他经历了手术后的麻性大肠,并在手术后的第27天出院.
结论:
- 在患有血管埃勒斯-丹洛斯综合征的患者中,鱼骨摄入后的胃肠道穿孔是极其罕见的事件.
- 有效的管理取决于仔细的诊断评估,个性化手术规划和优化的术后护理,以减轻严重并发症的风险并确保良好的结果.
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