Features of diagnosis and treatment of a child with choledochal cyst IС type

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Abstract

Choledochal cysts are congenital cystic dilatations of the extrahepatic and/or intrahepatic bile ducts. Diagnosis and choice of treatment tactics for this pathology often cause difficulties. A case report of a choledochal cyst in a 2-year-old patient with symptoms of recurrent jaundice, cholangitis, and pancreatitis, which required laparoscopic cholecystostomy and cholangiography during preparation for radical surgery, was retrospectively analyzed. The child was re-admitted to the pediatric surgical department with complaints of hyperthermia up to 39°C, resumption of periodic abdominal pain, nausea, and increased icterus of the sclera and skin. Laboratory and ultrasound examination indicated biliary and pancreatic hypertension. Choledochal cyst, cholestasis syndrome, acute cholecystopancreatitis was diagnosed. Owing to the existing clinical symptoms and laboratory and ultrasound data, laparoscopic cholecystostomy was urgently performed. Against the background of conservative therapy, within 2 days after laparoscopic cholecystostomy, clinically, laboratory and according to control ultrasound examination, biliary and pancreatic hypertension were stopped. The child underwent cholangiography through a cholecystostomy without additional anesthesia, which revealed a fusiform dilatation of the common hepatic and bile ducts. After 2 weeks of drug treatment against the background of laparoscopic cholecystostomy, the child underwent excision of the common bile duct cyst, and cholecystectomy with hepatic enteroanastomosis on a Roux-en-Y loop. The postoperative period was smooth. No other complaints or complications were noted within 24 months. In the reported case, recurrent obstructive jaundice was caused by a choledochal cyst. Laparoscopic cholecystostomy enabled the quick and successful relief of biliary hypertension, preparation of the patient for radical surgical treatment, and safe informative cholangiography through cholecystostomy. Hepatic enteroanastomosis with a disconnected loop according to Roux-en-Y was an effective surgical treatment method for choledochal cyst.

 

About the authors

Aleksey G. Sinitsyn

Volgograd State Medical University; Clinical Emergency Hospital No. 7

Email: all-sur04@mail.ru
ORCID iD: 0000-0002-8308-8364
SPIN-code: 3223-7231

MD, Cand. Sci. (Medicine)

Russian Federation, Volgograd; Volgograd

Andrei I. Perepelkin

Volgograd State Medical University; Clinical Emergency Hospital No. 7

Author for correspondence.
Email: similipol@mail.ru
ORCID iD: 0000-0001-5964-3033
SPIN-code: 5545-8353

MD, Dr. Sci. (Medicine), Professor

Russian Federation, Volgograd; Volgograd

Gleb A. Kopan

Volgograd State Medical University; Clinical Emergency Hospital No. 7

Email: gleb.kopan@yandex.ru
ORCID iD: 0000-0002-6627-1028
SPIN-code: 1465-6360

MD, Cand. Sci. (Medicine)

Russian Federation, Volgograd; Volgograd

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Supplementary files

Supplementary Files
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1. JATS XML
2. Fig. 1. Ultrasound at admission with signs of biliary hypertension: a — enlargement of the common bile duct up to 8–9 mm, in the terminal section up to 6 mm; b — enlargement of the right hepatic duct up to 4–5 mm; c — enlargement of the left hepatic duct up to 3 mm, segmental bile ducts up to 1.5 mm

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3. Fig. 2. Ultrasound control after relief of signs of biliary hypertension: a — common bile duct in the upper third — 7 mm (marked with an asterisk), in the middle third — 13 mm, in the lower third — 9 mm; b — cholecystostoma (indicated by arrow)

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4. Fig. 3. Cholecystocholangiography through cholecystostomy. Type IC choledochal cyst

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