Treatment of complex complications after choledochal cyst resection by multiple minimal invasive therapies: A case report

Nguyen, Hoa Viet; Hai, Dang; Nguyen, Hung Van; Vu, Tuan Hong; Hong, Quan Quy; Vo, Chung Ta; Dang, Trang Huyen Thi; Nguyen, Ngoc Bich; Le, Dung Tien; Tran, Phuong Ha Lien; Nguyen, Lan Thi Ngoc

doi:10.1016/j.ijscr.2020.06.104

Cited by 5 publications

(2 citation statements)

References 16 publications

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“…Especially when recurrent cholangitis or hepatolithiasis occurs after CM surgery, a biliary-enteric anastomotic stricture should be ruled out with magnetic resonance cholangiopancreatography (MRCP). A verified anastomotic stricture is primarily managed with endoscopic or transhepatic balloon dilation with a high success rate, while reoperation on is considered as a secondary option 131 . Tsuchida et al 132 described variant types of intrahepatic bile duct (IHD) anatomy associated with postoperative intrahepatic cholelithiasis.…”

Section: Hepatobiliarymentioning

confidence: 99%

Major surgical conditions of childhood and their lifelong implications: comprehensive review

Cullis,

Fouad,

Goldstein

et al. 2024

BJS Open

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Background In recent decades, the survival of children with congenital anomalies and paediatric cancer has improved dramatically such that there has been a steady shift towards understanding their lifelong health outcomes. Paediatric surgeons will actively manage such conditions in childhood and adolescence, however, adult surgeons must later care for these ‘grown-ups’ in adulthood. This article aims to highlight some of those rare disorders encountered by paediatric surgeons requiring long-term follow-up, their management in childhood and their survivorship impact, in order that the adult specialist may be better equipped with skills and knowledge to manage these patients into adulthood. Methods A comprehensive literature review was performed to identify relevant publications. Research studies, review articles and guidelines were sought, focusing on the paediatric management and long-term outcomes of surgical conditions of childhood. The article has been written for adult surgeon readership. Results This article describes the aforementioned conditions, their management in childhood and their lifelong implications, including: oesophageal atresia, tracheo-oesophageal fistula, malrotation, short bowel syndrome, duodenal atresia, gastroschisis, exomphalos, choledochal malformations, biliary atresia, Hirschsprung disease, anorectal malformations, congenital diaphragmatic hernia, congenital lung lesions and paediatric cancer. Conclusion The increasing survivorship of children affected by surgical conditions will translate into a growing population of adults with lifelong conditions and specialist healthcare needs. The importance of transition from childhood to adulthood is becoming realized. It is hoped that this timely review will enthuse the readership to offer care for such vulnerable patients, and to collaborate with paediatric surgeons in providing successful and seamless transitional care.

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Section: Hepatobiliarymentioning

confidence: 99%

Major surgical conditions of childhood and their lifelong implications: comprehensive review

Cullis,

Fouad,

Goldstein

et al. 2024

BJS Open

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“…The advancement of surgical treatment to include cyst excision has resulted in minimal morbidity and mortality and reduced the number of late complications, compared with past operative treatment of cystenterostomy. The most common short-term outcome in hepaticoenterostomy is anastomotic leakage and as a late complication continues to be anastomotic stricture (2.5-17%) and cholangitis (23-40%) [68][69][70][71].…”

Section: Outcome and Complicationsmentioning

confidence: 99%

Choledochal Cyst: Clinical Features, Diagnosis and Treatment Perspectives

Torres¹,

Becerra²,

Calderón³

et al. 2023

Biliary Tract - Review and Recent Progress

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Choledochal cyst is a congenital or acquired anomaly affecting the biliary tree in which exists a dilatation of the bile duct, not only the choledochus is affected but also the intrahepatic and extrahepatic ducts might be affected. The clinical presentation is not specific, even the classic triad with abdominal pain, mass, and jaundice is not common as suspected, found only in 10% of cases. Clinicians must rely on imaging studies for diagnosis and classification. The treatment is cyst excision with hepaticoenterostomy in most of the cases, but in some others, a liver transplant would be necessary. These patients require lifelong follow-up due to its rate of recurrence compared with general population.

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Diagnosis and Treatment of Choledochal Cysts: A Comprehensive Review with a Focus on Choledochocele

Ciccioli,

Mazza,

Sorge

et al. 2024

Dig Dis Sci

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Treatment of complex complications after choledochal cyst resection by multiple minimal invasive therapies: A case report

Cited by 5 publications

References 16 publications

Major surgical conditions of childhood and their lifelong implications: comprehensive review

Major surgical conditions of childhood and their lifelong implications: comprehensive review

Choledochal Cyst: Clinical Features, Diagnosis and Treatment Perspectives

Diagnosis and Treatment of Choledochal Cysts: A Comprehensive Review with a Focus on Choledochocele

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