WeBSurg, the e-surgical reference of Laparoscopic surgery
Clinical Case
HEPATIC CYSTPr D Mutter, Dr F Jamali, Hôpitaux Universitaires de Strasbourg, Strasbourg, France 1. DescriptionLiver cysts are common, congenital, benign entities. The workup and management of large non-parasitic liver cysts including the laparoscopic approach are illustrated in this case. 2. KeywordsHepatic cyst, benign cyst, laparoscopic fenestration 3. PatientMale, 45-year-old 4. Past medical historyKnown polycystic liver disease 5. History of present illnessThe patient presents with a sensation of fullness in the upper abdomen associated with early satiety. She denies abdominal pain, fever or weight loss. There is no nausea or vomiting. The fullness sensation is aggravated in the supine position and the patient can palpate a distinct epigastric mass. 6. Physical examinationConfirms the presence of a firm movable mass in the epigastrium with no suspicious adenopathy. The remainder of the exam is normal. 7. Laboratory valuesScreening laboratory values including liver function tests are within normal limits. 8. CT scanMultiple cysts in both lobes of the liver, with a dominant large cyst occupying segment II and III, measuring 10 x 7 x 11 cm. 9. ProcedureThe patient undergoes a laparoscopic cyst fenestration. This brief video illustrates the procedure. ![]() Video 9 10. DiscussionLiver cysts are common, congenital, benign entities that occur more frequently in the right lobe. They are for the most part small in size and occur four times as frequently in females as in males. The most common presenting symptoms of large cysts are increased abdominal girth, vague pain, occasional bleeding or infection and rarely obstructive jaundice. Small asymptomatic cysts generally require no treatment. The preferred treatment of large cysts from which clear fluid is aspirated is excision. However, in cases of proximity of major vascular or ductal structures, unroofing and external drainage are also used. If the cyst contains biliary contents, a communication to the bile duct system should be presumed and excision or Roux-en-Y cystojejunostomy becomes the treatment of choice. Polycystic liver disease often accompanies polycystic kidney disease. The number of cysts varies and rarely results in liver function compromise. Rupture, hemorrhage, and infection are rare. Simple aspiration of these multiple cysts is rarely effective. The surgical procedure of choice for a symptomatic dominant cyst in polycystic disease is the fenestration operation, in which the symptomatic cyst is made to communicate with the peritoneal cavity. The laparoscopic approach to the management of non-parasitic cystic disease of the liver has been popularized lately. Several publications attest to its safety and feasibility. The recurrence rate after laparoscopic fenestration is highly variable but ranges from 11-40% in the various series. Transposition of an omental flap into the remaining cyst cavity has been described to minimize recurrences but its effectiveness remains unproven. Factors predicting failure include previous surgical treatment, deep-seated cysts, incomplete unroofing, location in the right posterior segments of the liver, and a diffuse form of PLD with small cysts. 11. References
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