胎儿大管状食管重复囊肿:病例报告

Q3 Medicine
Călina Maier, Radu Vlădăreanu, Raluca Tocariu, Marcela Șerban, Maria Olincă, Elvira Brătilă
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引用次数: 0

摘要

导言 食管重复囊肿(EDC)是一种罕见的先天性畸形,仅次于神经元肿瘤,是导致儿童后部肿块的第二大常见原因,发病率约为 1/22,500。宫颈囊肿非常罕见,产前检查也相当少见。 方法 我们报告了一例在产前 3 个月诊断出的孤立性纵隔和宫颈管状EDC。 结果 婴儿出生后,由于囊肿增大而出现呼吸困难症状,她接受了肿块切除术。术后情况良好。 结论 我们的目的是提高人们对这种疾病的超声波特征的认识,从而提高产前诊断率,并就预后和出生后进一步采取多学科方法的必要性为父母提供适当的咨询。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Fetal large tubular oesophageal duplication cyst: A case report

Fetal large tubular oesophageal duplication cyst: A case report

Introduction

Oesophageal duplication cyst (EDC) is a rare congenital anomaly representing, after neuronal tumours, the second most common cause of posterior mass in children, with a prevalence of approximately 1/22,500 live births. Cervical cysts are very rare, and their antenatal detection is fairly uncommon.

Methods

We report the case of an isolated large mediastinal and cervical tubular EDC diagnosed prenatally in the third trimester.

Results

After birth, the baby became symptomatic developing respiratory distress due to the enlargement of the cyst and she underwent excision of the mass. The post-operative evolution was very good.

Conclusion

Our purpose was to raise awareness of the ultrasonographic features of this condition, thus improving the rate of prenatal diagnosis and offering the parents a proper counselling regarding the prognosis and the need for a further multidisciplinary approach after birth.

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来源期刊
Australasian Journal of Ultrasound in Medicine
Australasian Journal of Ultrasound in Medicine Medicine-Radiology, Nuclear Medicine and Imaging
CiteScore
1.90
自引率
0.00%
发文量
40
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