Fig. 2: The four main types of gallbladder duplication. Top left: Double gallbladder with a Y-shaped cystic duct entering the common bile duct. Top right: Double gallbladder with independent cystic duct entering the common bile duct. Bottom left: The second gallbladder is connected by its own cystic duct in the left hepatic duct. Bottom right: The cystic duct of the duplicated gallbladder enters the right lobe of the liver to connect with the right hepatic duct.
Associated anomalies
Several anomalies have been associated with gallbladder duplication including forgut malformations and aberrant hepatic and mesenteric vessels2,3. Sonographic distinction between types of duplications (i.e. anatomy of cystic ducts) and detection of aberrant vessels has not been reported in the literature.
Prior to ultrasound, gallbladder duplications often were diagnosed only at the time of surgery, but sonography has described several cases in children and adults5.
Differential diagnosis
The differential diagnosis of gallbladder duplication (Table I) from other right upper quadrant cystic lesions is difficult.
Table 1: Differential diagnosis of gallbladder duplication
- Gallbladder folds
- Choledochal cyst
- Gallbladder diverticulum
- Hepatic cyst
- Mesenteric cyst
In adults, the presence of stones and the observation of asymmetric contraction of the gallbladder can aid in differentiation of folds from duplication7. Differentiation in symptomatic patients, with hepatobiliary imaging also has been recommended6. Also, CT evaluation of the gallbladder and associated vascular anomalies is reported to aid in the diagnosis of gallbladder duplication3. In neonates, ultrasound remains the modality of choice.
Congenital hepatic cysts are rare (less than 2% occur in children less than 2 years old), and they usually occur in the anterior segment of the right lobe. Gallbladder folds are commonly transverse and therefore the appearance is different from the longitudinal division observed in this case. Choledochal cysts are not expected to lie along the gallbladder as in this case.
Prognosis
The prognosis for gallbladder duplication is good. Although several authors report increased risk of acute and chronic cholecystitis, cholesterolosis, papilloma, carcinoma, biliary cirrhosis and torsion, other reports did not confirm this increased risk2-8.
Therefore, when gallbladder duplication is discovered in utero, the patient can be reassured as to the benignancy of the finding.
References
1. Boyden E.A. The accessory gallbladder. Am J Anat 1926;38:177-231.
2. Udelsman R. Congenital duplication of gallbladder associated with an anomalous right hepatic artery. Am J Surg 1985;149:812-815.
3. Nichols DM, Superior mesentric vein rotation: a CT sign of mid-gut malrotation. AJR 1983;141:707-8.
4. Ryrberg C.H. Gallbladder duplication. Acta Chir Scand 1960;119:36-44.
5. Granot E. Duplication of gallbladder associated with childhood obstructive biliary disease and biliary cirrhosis. Gastroenterology 1983;85:946-950.
6. McDonald K, Sonographic and Scintigraphic evaluation of gallbladder duplication. Clin Nucl Med 1986;11(10); 692-693.
7. Gioncy, Sonography of gallbladder duplication and differential condiderations. AJR 145;241-3, 1985.
8. Harlaftis N. Multiple gallbladders. Surg Gynecol Obstet 1977;145:928-934.
9. Gross RE. Congential anomalies of the gallbladder: a review of 148 cases with a report of double gallbladder. Arch Surg 32:131, 1936.
10. Jastrow M Jr. The liver as the seat of the soul. lr: Lyon, Moore, eds. Studies in the history of religions. New York, MacMillen 1912:160.
11. Kurzewg FT, Cole PA. Triplication of the gallbladder: review of literature and report of a case. Am Surg 1979;45:410.