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[脐尿管未闭的产前诊断与演变]

[Prenatal diagnosis and evolution of patent urachus].

作者信息

Mazeau P, Curinier S, Kandem-Simo A, Delabaere A, Laurichesse H, Lemery D, Gallot D

机构信息

Pôle gynéco-obstétrique-reproduction humaine, CHU Estaing, 1, place Lucie-Aubrac, 63003 Clermont-Ferrand cedex 1, France.

Service de chirurgie pédiatrique, pôle de pédiatrie, CHU Estaing, 1, place Lucie-Aubrac, 63003 Clermont-Ferrand cedex 1, France.

出版信息

J Gynecol Obstet Biol Reprod (Paris). 2014 May;43(5):393-6. doi: 10.1016/j.jgyn.2013.02.005. Epub 2013 Mar 19.

DOI:10.1016/j.jgyn.2013.02.005
PMID:23523249
Abstract

Prenatal ultrasonographic features of patent urachus consist in anechoic proximal cord cyst communicating with the bladder associated with large umbilicus. Distinction should be made with omphalocele and bladder extrophy. Spontaneous evolution leads to rupture during mid-trimester and bladder protrusion. Karyotyping is not mandatory in isolated typical cases. Early postnatal surgery is usually required.

摘要

脐尿管未闭的产前超声特征表现为近端脐带囊肿呈无回声,与膀胱相通,并伴有脐部增大。应与脐膨出和膀胱外翻相鉴别。自然演变会导致在孕中期破裂及膀胱突出。对于孤立的典型病例,不强制进行染色体核型分析。通常需要在出生后早期进行手术。

相似文献

1
[Prenatal diagnosis and evolution of patent urachus].[脐尿管未闭的产前诊断与演变]
J Gynecol Obstet Biol Reprod (Paris). 2014 May;43(5):393-6. doi: 10.1016/j.jgyn.2013.02.005. Epub 2013 Mar 19.
2
Prenatally Ruptured Patent Urachus: A Case Report and Review of Literature.产前破裂的先天性脐尿管:病例报告及文献复习。
Medicina (Kaunas). 2022 Nov 10;58(11):1621. doi: 10.3390/medicina58111621.
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Prenatal management of an allantoic cyst with patent urachus.脐尿管未闭合并尿囊囊肿的产前管理
Arch Gynecol Obstet. 2009 Aug;280(2):321-3. doi: 10.1007/s00404-008-0909-8. Epub 2009 Jan 6.
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Unusual fate of vesicoallantoic cyst with non-visualization of fetal urinary bladder in a case of patent urachus.脐尿管未闭病例中膀胱脐尿管囊肿的异常转归及胎儿膀胱不可见
Ultrasound Obstet Gynecol. 1997 Jun;9(6):422-4. doi: 10.1046/j.1469-0705.1997.09060422.x.
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Prenatal and Postnatal Clinical Course of an Urachus Identified as an Allantoic Cyst in the Umbilical Cord.产前及产后经诊断为脐带尿囊囊肿的脐尿管临床病程
Eur J Pediatr Surg. 2016 Apr;26(2):200-2. doi: 10.1055/s-0035-1549263. Epub 2016 Mar 16.
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Prenatally diagnosed patent urachus with bladder prolapse.产前诊断为脐尿管未闭合并膀胱脱垂。
J Pediatr Surg. 2007 Dec;42(12):e7-10. doi: 10.1016/j.jpedsurg.2007.07.055.
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Prenatal diagnosis of a patent urachus cyst with the use of 2D, 3D, 4D ultrasound and fetal magnetic resonance imaging.利用二维、三维、四维超声及胎儿磁共振成像对脐尿管囊肿进行产前诊断。
Fetal Diagn Ther. 2008;24(4):444-7. doi: 10.1159/000174572. Epub 2008 Nov 20.
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Prenatally diagnosed ruptured vesico-allantoic cyst presenting as patent urachus at birth.产前诊断为膀胱尿囊囊肿破裂,出生时表现为脐尿管未闭。
J Urol. 2003 Apr;169(4):1478-9. doi: 10.1097/01.ju.0000053927.08111.2d.
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Persistent patent urachus with allantoic cyst: a case report.伴有尿囊囊肿的持续性脐尿管未闭:一例报告
Ultrasound Obstet Gynecol. 1997 Nov;10(5):366-8. doi: 10.1046/j.1469-0705.1997.10050366.x.
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Prenatally diagnosed patent urachus with umbilical cord cyst and early surgical intervention.产前诊断为脐尿管未闭合并脐带囊肿及早期手术干预。
Ceska Gynekol. 2019 Winter;84(6):425-429.

引用本文的文献

1
Omphalocele Secondary to Spontaneous Rupture of Allantoic Cyst in the Third Trimester of Pregnancy.妊娠晚期尿囊囊肿自发性破裂继发脐膨出
Case Rep Obstet Gynecol. 2021 Sep 18;2021:6940685. doi: 10.1155/2021/6940685. eCollection 2021.
2
ALK-negative urachal inflammatory myofibroblastic tumor in an elderly female: A case report.老年女性的ALK阴性脐尿管炎性肌纤维母细胞瘤:一例报告
Medicine (Baltimore). 2018 Dec;97(51):e13619. doi: 10.1097/MD.0000000000013619.