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胆管假性囊肿：胆管囊肿前体产前穿孔的一种罕见并发症。

Biliary Pseudocyst: A Rare Complication of Antenatal Perforation of Forme Fruste Choledochal Cyst.

作者信息

Arora Mrinal, Kaur Jaswinder, Aggarwal Satish Kumar

机构信息

Department of Pediatric Surgery, Sir Ganga Ram Hospital, New Delhi, India.

Department of Pediatrics, Sir Ganga Ram Hospital, New Delhi, India.

出版信息

J Indian Assoc Pediatr Surg. 2019 Oct-Dec;24(4):291-293. doi: 10.4103/jiaps.JIAPS_212_18.

DOI:10.4103/jiaps.JIAPS_212_18
PMID:31571763
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6752079/
Abstract

Spontaneous perforation of choledochal cyst (CDC) is rare with an incidence of 1.8%-7%. Perforation with pseudocyst formation is even rarer, there being only two case reports. We report the first case of antenatal perforation of CDC with biliary pseudocyst formation in a newborn and its management.

摘要

胆总管囊肿（CDC）自发性穿孔较为罕见，发生率为1.8%-7%。伴有假性囊肿形成的穿孔更为罕见，仅有两篇病例报告。我们报告了首例新生儿期发生的伴有胆汁性假性囊肿形成的CDC产前穿孔病例及其处理情况。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/75e2/6752079/362c4635ed12/JIAPS-24-291-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/75e2/6752079/0deee908bc2c/JIAPS-24-291-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/75e2/6752079/362c4635ed12/JIAPS-24-291-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/75e2/6752079/0deee908bc2c/JIAPS-24-291-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/75e2/6752079/362c4635ed12/JIAPS-24-291-g002.jpg

相似文献

1
Biliary Pseudocyst: A Rare Complication of Antenatal Perforation of Forme Fruste Choledochal Cyst.胆管假性囊肿：胆管囊肿前体产前穿孔的一种罕见并发症。
J Indian Assoc Pediatr Surg. 2019 Oct-Dec;24(4):291-293. doi: 10.4103/jiaps.JIAPS_212_18.
2
A very low-birth-weight infant with spontaneous perforation of a choledochal cyst and adjacent pseudocyst formation.极低出生体重儿自发性胆总管囊肿穿孔并邻近假性囊肿形成。
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Choledochal cyst rupture with an intrahepatic pseudocyst mimicking hepatic mesenchymal hamartoma in an infant.婴儿胆总管囊肿破裂伴肝内假性囊肿，类似肝间叶性错构瘤。
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引用本文的文献

1
Value of serum GGT level in the timing of diagnosis of choledochal cyst perforation.血清γ-谷氨酰转移酶水平在胆总管囊肿穿孔诊断时机中的价值
Front Pediatr. 2022 Aug 15;10:921853. doi: 10.3389/fped.2022.921853. eCollection 2022.

本文引用的文献

1
Choledochal cyst rupture with an intrahepatic pseudocyst mimicking hepatic mesenchymal hamartoma in an infant.婴儿胆总管囊肿破裂伴肝内假性囊肿，类似肝间叶性错构瘤。
Clin Imaging. 2015 Sep-Oct;39(5):914-6. doi: 10.1016/j.clinimag.2015.04.016. Epub 2015 May 7.
2
A very low-birth-weight infant with spontaneous perforation of a choledochal cyst and adjacent pseudocyst formation.极低出生体重儿自发性胆总管囊肿穿孔并邻近假性囊肿形成。
J Pediatr Surg. 2012 Jul;47(7):E17-9. doi: 10.1016/j.jpedsurg.2012.03.055.
3
Spontaneous perforation of choledochal cyst: a case with unusual distribution of fluid in the retroperitoneal space.
胆总管囊肿自发性穿孔：一例腹膜后间隙液体分布异常的病例
Pediatr Radiol. 2009 Jun;39(6):629-31. doi: 10.1007/s00247-009-1189-6. Epub 2009 Feb 25.
4
Choledochal cyst disease. A changing pattern of presentation.胆总管囊肿疾病。临床表现的变化模式。
Ann Surg. 1994 Nov;220(5):644-52. doi: 10.1097/00000658-199411000-00007.
5
Choledochal cyst.胆总管囊肿
Curr Probl Surg. 1992 Jun;29(6):361-410. doi: 10.1016/0011-3840(92)90025-x.