双边宫肋形成伪关节炎,第一个肋骨与异常的右下关节动脉同时发生
Bartosz Kołodziejczyk1,2, Izabela Zamojska3, Joanna Jaworek-Troć3
1Department of Anatomy, Jagiellonian University Medical College, Cracow, Poland. bartosz.kolodziejczyk@uj.edu.pl.
Folia morphologica
|March 4, 2026
概括
本案例报告强调了双边完整的椎肋骨和异常的右下关节动脉的罕见同时出现. 它们的联合存在可能表明它们具有共同的遗传起源,并影响血管程序.
科学领域:
- 人体解剖学 解剖学 解剖学
- 血管外科 血管外科
- 遗传学 遗传学 是一个
背景情况:
- 大动脉弧分支和胸发育的解剖学变异是常见的.
- 宫肋骨和异常下关节动脉 (arteria lusoria) 的共存报告不足.
- 这些异常可能是由细分发育中断引起的.
研究的目的:
- 报告一个同时存在的双边完整的椎肋骨和门动脉的病例.
- 讨论潜在的共同遗传机制.
- 突出其对血管通透性和外科手术程序的影响.
主要方法:
- 一个70岁的波兰妇女的病例报告.
- 宫肋骨和异常的右下关节动脉的详细解剖描述.
- 关于患病率和潜在遗传联系的文献综述.
主要成果:
- 这位患者出现了双边完整的宫肋骨,与第一个肋骨形成了伪关节炎.
- 一个逆食道异常右下关节动脉 (arteria lusoria) 被确定.
- 异常的组合可能对动脉产生协同效应.
结论:
- 这些异常的同时发生可能比预期的更频繁.
- 血管和骨发育障碍的共同遗传基础是可信的.
- 这种组合对右下关节动脉通透性构成风险,并使血管内干预复杂化.
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