肺小,挑战大:引导胎儿胸腔积液结局,长期随访和对未来妊娠的影响。

Charu Sharma, Shreya Das, Kalika Dubey, Dolat Singh Shekhawat, Meenakshi Gothwal, Shashank Shekhar, Pratibha Singh, Kuldeep Singh
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引用次数: 0

摘要

摘要胎儿胸腔积液是一种罕见的胎儿胸腔积液。侵入性手术需要排除染色体异常和感染,因为治疗延误会导致严重的胎儿并发症。我们讨论了一个30岁的初产妇在妊娠20周出现胎儿双侧胸腔积液和轻度腹水的病例。妊娠23周行胸穿刺,发现乳糜胸。胸腔积液于28周后自行消退。在36周时,严重的羊水过少促使紧急剖腹产。产后基因检测发现了两种不确定意义的变异。婴儿病情好转并于第六天出院,在3.5年的随访中没有出现并发症。这对夫妇随后的怀孕并不复杂。我们提出了一个循序渐进的治疗方案,强调通过超声和细胞学分析进行早期诊断,然后在严重的病例中进行胸腔穿刺术。定期随访对于监测流体动力学和根据需要调整管理至关重要。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Tiny Lungs, Big Challenges: Navigating Fetal Pleural Effusion Outcomes, Long Term Follow-up and Implications for Future Pregnancies.

Tiny Lungs, Big Challenges: Navigating Fetal Pleural Effusion Outcomes, Long Term Follow-up and Implications for Future Pregnancies.

Tiny Lungs, Big Challenges: Navigating Fetal Pleural Effusion Outcomes, Long Term Follow-up and Implications for Future Pregnancies.

Fetal pleural effusion is a rare condition involving fluid accumulation in the pleural cavity of the fetus. Invasive procedures are required to exclude chromosomal anomalies and infections, as treatment delays can lead to severe fetal complications. We discuss a case where a 30-year-old primigravida presented at 20 weeks gestation with fetal bilateral pleural effusion and mild ascites. At 23 weeks of gestation, thoracocentesis was performed which revealed chylothorax. The pleural effusion resolved spontaneously by 28 weeks. At 36 weeks, severe oligohydramnios prompted an emergency caesarean section. Postnatal genetic testing found two variants of uncertain significance. The baby improved and was discharged on day six, with no complications over 3.5 years of follow-up. The couple's subsequent pregnancy was uncomplicated. We propose a stepwise management protocol emphasising early diagnosis through ultrasound and cytological analysis, followed by thoracocentesis in severe cases. Regular follow-up is essential to monitor fluid dynamics and adjust management as needed.

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