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超声产前诊断巨大十二指肠:1 例报告。

Prenatal diagnosis of megaduodenum using ultrasound: a case report.

机构信息

Department of Ultrasound, Shengjing Hospital of China Medical University, No.36 Sanhao St, Shenyang, 110004, Liaoning, China.

Department of Ultrasound, Shenyang Women's and Children's Hospital, Shenyang, Liaoning, China.

出版信息

BMC Pregnancy Childbirth. 2021 May 11;21(1):370. doi: 10.1186/s12884-021-03843-0.

DOI:10.1186/s12884-021-03843-0
PMID:33975544
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8111774/
Abstract

BACKGROUND

Congenital megaduodenum is a rare disorder; however, its prenatal diagnosis has not been reported previously. We report the case of an abdominal cystic mass in a fetus that was later diagnosed as megaduodenum.

CASE PRESENTATION

An abdominal cystic mass was found during ultrasonography of a fetus at 11 weeks of gestation. The mass progressively enlarged with gestation. The amniotic fluid volume decreased and then returned to normal. During the last prenatal ultrasound examination, the mass was observed communicating with the stomach; therefore, duodenal dilation was suspected. Finally, the patient was diagnosed with megaduodenum caused by a developmental defect in the nerve plexus.

CONCLUSIONS

Congenital megaduodenum is a differential diagnosis of massive fetal abdominal cystic masses. Ultrasound examinations of such masses communicating with the stomach may help determine the diagnosis.

摘要

背景

先天性巨十二指肠是一种罕见的疾病,但以前没有报道过其产前诊断。我们报告了一例胎儿腹部囊性肿块的病例,该病例后来被诊断为巨十二指肠。

病例介绍

在胎儿 11 周妊娠的超声检查中发现腹部囊性肿块。肿块随妊娠逐渐增大。羊水体积减少,然后恢复正常。在最后一次产前超声检查中,观察到肿块与胃相通,因此怀疑存在十二指肠扩张。最终,患者被诊断为神经丛发育缺陷引起的先天性巨十二指肠。

结论

先天性巨十二指肠是胎儿腹部巨大囊性肿块的鉴别诊断之一。与胃相通的此类肿块的超声检查有助于确定诊断。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cc80/8111774/3b8e86bbe577/12884_2021_3843_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cc80/8111774/1d269c25daf0/12884_2021_3843_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cc80/8111774/4562952e8ffd/12884_2021_3843_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cc80/8111774/3b8e86bbe577/12884_2021_3843_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cc80/8111774/1d269c25daf0/12884_2021_3843_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cc80/8111774/4562952e8ffd/12884_2021_3843_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cc80/8111774/3b8e86bbe577/12884_2021_3843_Fig3_HTML.jpg

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Ultraschall Med. 2022 Apr;43(2):194-203. doi: 10.1055/a-1194-4363. Epub 2020 Jun 23.
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A rare case of idiopathic congenital megaduodenum in adult misinterpreted during childhood: case report and literature review.一例成人特发性先天性巨十二指肠罕见病例在儿童期被误诊:病例报告及文献综述
Radiol Case Rep. 2019 May 9;14(7):858-863. doi: 10.1016/j.radcr.2019.04.016. eCollection 2019 Jul.
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Megaduodenum in a 59-year-old man: a very late postoperative complication after duodenal atresia.
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BMJ Case Rep. 2018 Jan 18;2018:bcr-2017-221792. doi: 10.1136/bcr-2017-221792.
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A Rare Case of Megaduodenum Associated With a Duodenal Trichobezoar.一例罕见的与十二指肠毛粪石相关的巨十二指肠病例。
J Pediatr Gastroenterol Nutr. 2017 Feb;64(2):e50-e51. doi: 10.1097/MPG.0000000000000583.
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Acta Chir Belg. 2016 Oct;116(5):305-308. doi: 10.1080/00015458.2016.1147263. Epub 2016 Jul 5.
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IMAGES IN CLINICAL MEDICINE. Megaduodenum in Systemic Sclerosis.临床医学影像。系统性硬化症中的巨十二指肠
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