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先天性膈疝作为妊娠晚期心肺功能衰竭和内脏梗阻的原因。

Congenital diaphragmatic hernia as a cause of cardiorespiratory failure and visceral obstruction in late pregnancy.

作者信息

Barbetakis Nikolaos, Efstathiou Andreas, Vassiliadis Michalis, Fessatidis Ioannis

机构信息

Cardiothoracic Surgical Department, Geniki Kliniki-Euromedica, Thessaloniki, Greece.

出版信息

J Gastrointestin Liver Dis. 2006 Jun;15(2):185-8.

Abstract

BACKGROUND

Diaphragmatic hernia complicating pregnancy is rare and results in a high mortality rate, particularly if early surgical intervention is not undertaken.

CASE PRESENTATION

A woman at 23 week gestation was admitted with symptoms of respiratory failure and bowel obstruction due to incarceration of viscera through a left posterolateral defect of the diaphragm (Bochdalek's hernia). Surgery (left thoracoabdominal incision) demonstrated compression atelectasis, mediastinal shift, strangulation and gangrene of the herniated viscera which led to segmental resection of the involved portion of large intestine with re-establishment of bowel continuity by end to end anastomosis. The greater omentum was partly necrotic necessitating resection. The diaphragmatic defect was closed with interrupted sutures. Postoperative period was uncomplicated. Pregnancy was allowed to continue until 39 weeks' gestation at which time elective cesarean delivery was performed.

CONCLUSION

Symptomatic maternal diaphragmatic hernia during pregnancy is a surgical emergency and requires a high index of suspicion.

摘要

背景

妊娠合并膈疝较为罕见,死亡率很高,尤其是未进行早期手术干预时。

病例报告

一名妊娠23周的女性因内脏通过左侧后外侧膈肌缺损(博赫dalek疝)嵌顿而出现呼吸衰竭和肠梗阻症状入院。手术(左胸腹联合切口)显示受压性肺不张、纵隔移位、疝入内脏绞窄和坏疽,导致对受累大肠部分进行节段性切除,并通过端端吻合重建肠道连续性。大网膜部分坏死,需要切除。膈肌缺损用间断缝合关闭。术后过程顺利。妊娠持续至39周,此时进行了择期剖宫产。

结论

妊娠期有症状的母体膈疝是外科急症,需要高度怀疑。

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