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1.
Pediatr Surg Int ; 40(1): 183, 2024 Jul 11.
Article in English | MEDLINE | ID: mdl-38992296

ABSTRACT

PURPOSE: To describe clinical features of choledochal cyst (CC) patients in terms of demographic data, clinical presentation, investigations, treatment, and outcomes among children and adults. METHODS: The medical records of patients undergoing choledochal cyst (CC) surgery from 2002 to 2021 at a university hospital were retrospectively reviewed. The patients were divided into two groups: children (< 15 years) and adults (≥ 15 years). Descriptive statistics were used. RESULTS: There were 106 cases of CC (Female/male = 88/18, children/adult = 53/53). Abdominal pain was the predominant presenting symptom, followed by jaundice in both groups. Adults were significantly more prone to present with abdominal pain compared to children (86.8% vs. 52.8%; p < 0.001), while children were more likely to experience acholic stool than adults (22.6% vs. 3.8%; p = 0.004). Ultrasound was the preferred investigation screening modality (75.5%). Most patients were presented with type I CC (71.7%). Laparoscopic-assisted approach was performed in 8.5%. CC excision with roux-en-y hepatico-jejunostomy was the main procedure (88.7%). Adults had a higher incidence of post-op complications, including stones, anastomosis stricture, abdominal collection, and cholangitis. Adults were significantly more likely to require intervention after surgery, compared to children (26.4% vs. 5.7%; p = 0.04). CONCLUSIONS: Ultrasound was the most common screening tool for diagnosis. Postoperatively, adults with CC experience more serious post-op complications compared to children. This could be attributed to long-standing cystic inflammation. Therefore, prompt definitive surgery is recommended for CC patients.


Subject(s)
Choledochal Cyst , Choledochal Cyst/diagnostic imaging , Choledochal Cyst/pathology , Choledochal Cyst/surgery , Retrospective Studies , Humans , Male , Child , Adult , Adolescent , Child, Preschool , Postoperative Complications , Treatment Outcome , Ultrasonography
2.
World J Gastroenterol ; 30(9): 1043-1072, 2024 Mar 07.
Article in English | MEDLINE | ID: mdl-38577180

ABSTRACT

Several diseases originate from bile duct pathology. Despite studies on these diseases, certain etiologies of some of them still cannot be concluded. The most common disease of the bile duct in newborns is biliary atresia, whose prognosis varies according to the age of surgical correction. Other diseases such as Alagille syndrome, inspissated bile duct syndrome, and choledochal cysts are also time-sensitive because they can cause severe liver damage due to obstruction. The majority of these diseases present with cholestatic jaundice in the newborn or infant period, which is quite difficult to differentiate regarding clinical acumen and initial investigations. Intraoperative cholangiography is potentially necessary to make an accurate diagnosis, and further treatment will be performed synchronously or planned as findings suggest. This article provides a concise review of bile duct diseases, with interesting cases.


Subject(s)
Bile Duct Diseases , Biliary Atresia , Choledochal Cyst , Infant , Child , Infant, Newborn , Humans , Bile Ducts/diagnostic imaging , Bile Ducts/surgery , Biliary Atresia/diagnosis , Biliary Atresia/surgery , Choledochal Cyst/diagnosis , Choledochal Cyst/diagnostic imaging , Bile Duct Diseases/diagnosis , Bile Duct Diseases/etiology , Bile Duct Diseases/therapy , Cholangiography
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