首页> 外文期刊>Journal of the Siena Academy of Sciences >PARTIAL CONGENITAL BOWEL OBSTRUCTION BY DUODENAL ATRESIA WINDSOCKS TYPE: CASE REPORT
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PARTIAL CONGENITAL BOWEL OBSTRUCTION BY DUODENAL ATRESIA WINDSOCKS TYPE: CASE REPORT

机译:十二指肠闭锁性小弓部分先天性肠梗阻类型:病例报告

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Introduction Duodenal atresia Windsocks type is a rare condition of congenital bowel obstruction. Thanks to recent technological advancements of prenatal diagnosis it is possible to make a diagnosis of duodenal atresia with high degree of certainty through the radiological sign of “double bubble”, but up to date it is not yet possible to identify the type of duodenal atresia. We report the case of a patient with prenatal diagnosis of “double bubble”. The patient had no other concomitant malformations. Case Report The patient came to our attention after prenatal ultrasound that showed a picture of double bubble. At the 27th week of gestation we performed fetal MRI that confirmed the US pattern of double bubble but it did not identify with certainty the type of duodenal atresia. At birth the patient underwent GI rx examination that showed a picture of partial duodenal obstruction compatible with the Windsocks type. On the following day, we performed endoscopy which showed the presence of duodenal membrane, so the patient underwent surgical treatment with a longitudinal duodenal incision in order to treat the wind-sock membrane. After one month a further Upper-GI rx examination showed a regular transit of the contrast. Four months after the first operation the patient underwent new surgical treatment for bowel obstruction by adhesions. The operation was successful and the patient had a complete recover. Conclusions Patients with prenatal diagnosis of “double bubble” require a multidisciplinary approach for proper clinical management. Unfortunately it is not currently possible to identify with certainty by prenatal ultrasound the type of duodenal atresia, but in case of incomplete bowel occlusion , the possibility of an atresia Windsocks type should always be considered, especially for setting the right surgical approach.
机译:简介十二指肠闭锁风向袋型是一种罕见的先天性肠梗阻情况。由于产前诊断的最新技术进步,可以通过“双泡”的放射学征象高度确定性地诊断十二指肠闭锁,但是迄今为止,尚无法确定十二指肠闭锁的类型。我们报告了一名产前诊断为“双泡”的患者。该患者没有其他伴随的畸形。病例报告产前超声检查显示双泡图像后,该患者引起了我们的注意。在妊娠的第27周,我们进行了胎儿MRI检查,证实了美国的双泡型,但不能确定十二指肠闭锁的类型。患者出生时接受了GI rx检查,显示出与Windsocks类型兼容的十二指肠局部梗阻的图像。第二天,我们进行了内窥镜检查,结果显示十二指肠膜的存在,因此该患者接受了纵向十二指肠切口的外科手术治疗,以治疗风向袋膜。一个月后,进一步的Upper-GI rx检查显示了对比剂的定期转移。首次手术四个月后,患者因粘连肠梗阻接受了新的外科治疗。手术成功,患者完全康复。结论产前诊断为“双泡”的患者需要采取多学科的方法来进行适当的临床治疗。不幸的是,目前尚无法通过产前超声确定十二指肠闭锁的类型,但在肠梗阻不完全的情况下,应始终考虑闭锁风向袋类型的可能性,尤其是在确定正确的手术方法时。

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