Type II choledochal cyst of the cystic duct in a 3 Month old

DeJesus, Jana E.; Hughes, Byron D.; Geisler, Emily L.; Defilippo, Christine; Gaffey, Jaclyn; Radhakrishnan, Ravi S.

doi:10.1016/j.epsc.2022.102440

Cited by 2 publications

(2 citation statements)

References 19 publications

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“…Table 1 shows the list of 26 Type VI CCs and their evaluation and management with respective reported authors. [ 5 ] So far, only 10 cases of this Type VI CCs are reported in children in the literature. This is the 11 th pediatric case report of Type VI CC.…”

Section: Discussionmentioning

confidence: 99%

Type VI Choledochal Cyst – An Emerging Rare Entity (11th Pediatric Case of Type VI) with a Review of Literature

Sushma,

Redkar,

Sharma

et al. 2023

Journal of Indian Association of Pediatric Surgeons

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A BSTRACT Choledochal cysts (CCs) are abnormal dilatations of the biliary system. Usually, CCs are classified into five types. The sixth type (Type VI) is an emerging and rare type, reported the first case in 1991. We report this rare CC, Type VI seen in our experience for the first time. We have also reviewed the literature; only 26 cases of Type VI were found, including adults and children, ever since the first case has been reported in 1991. To the best of our knowledge, this is the 11 th pediatric case report of a Type VI choledochal cyst.

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Section: Discussionmentioning

confidence: 99%

Type VI Choledochal Cyst – An Emerging Rare Entity (11th Pediatric Case of Type VI) with a Review of Literature

Sushma,

Redkar,

Sharma

et al. 2023

Journal of Indian Association of Pediatric Surgeons

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“…Previous researches have postulated the existence of an alteration in the pancreatobiliary junction with sphincter of Oddi dysfunction, which ends up favoring a reflux of pancreatic enzymes into the biliary system [7][8][9]. Nevertheless, there are other theories involving congenital weakness of the duct wall, mucosal abnormalities, obstruction of the distal biliary system, and even congenital infections [10][11][12].…”

Section: Introductionmentioning

confidence: 99%

Choledochal cyst with prenatal diagnosis and postnatal management: A case report

Torres¹,

Álvarez²

2022

Magna Sci. UCEVA

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Cystic dilatation of the bile duct is part of a wide spectrum of biliary pathology with different etiopathogenic mechanisms. Choledochal cysts are rare malformations of the bile ducts. It is diagnosed in most cases during early childhood, although it can present at any age of life. The clinical presentation is variable and can be manifested by abdominal pain, palpable mass, cholestatic jaundice or by symptoms linked to the development of some of its complications: pancreatitis, cholangitis or rupture. The diagnosis is made through abdominal ultrasound and is completed with a ,magnetic cholangiography the recommended treatment is complete surgical resection that prevents the appearance of complications. A case of ultrasound prenatal diagnosis is presented at 29 weeks of gestation along with its evolution, management and postnatal treatment, it is also the first case in this health center located in Valle del Cauca

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Type II choledochal cyst of the cystic duct in a 3 Month old

Cited by 2 publications

References 19 publications

Type VI Choledochal Cyst – An Emerging Rare Entity (11th Pediatric Case of Type VI) with a Review of Literature

Type VI Choledochal Cyst – An Emerging Rare Entity (11th Pediatric Case of Type VI) with a Review of Literature

Choledochal cyst with prenatal diagnosis and postnatal management: A case report

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