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DOI:10.2214/AJR.04.1270
AJR 2005; 185:1211-1213
© American Roentgen Ray Society


Case Report

Fistulous Communication Between a Hepatic Hydatid Cyst and the Gallbladder: Diagnosis with MR Cholangiopancreatography

Ibrahim Adaletli1, Serpil Yilmaz2, Yavuz Cakir2, Resat Kervancioglu2 and Metin Bayram2

1 Department of Radiology, Cerrahpasa Medical Faculty, Istanbul University, Kocamustafapasa, Istanbul 34300, Turkey.
2 Department of Radiology, Medical Faculty, Gaziantep University, Gaziantep, Turkey.

Received August 12, 2004; accepted after revision October 15, 2004.

 
Address correspondence to I. Adaletli.


Introduction
Top
Introduction
Case Report
Discussion
References
 
Communication of a hydatid disease with the biliary tree has been described in up to 90% of hepatic hydatid cysts [1]. This is due to the incorporation of biliary radicles into the pericyst [2]. However, frank rupture into the biliary tree occurs in only 5–15% of cases [1]. Although the communication with the intrahepatic bile ducts is common, its occurrence between a hepatic hydatid cyst and the gallbladder is rare [3].

We present an unusual case of a fistulous communication between a hepatic hydatid cyst and the gallbladder. The MR cholangiopancreatography (MRCP) features have been discussed.


Case Report
Top
Introduction
Case Report
Discussion
References
 
A 46-year-old man with complaints of right upper quadrant pain, fever, icterus associated with clay-colored stools, and itching was admitted with a diagnosis of obstructive cholangitis. Physical examination revealed tenderness in the epigastric region and right upper quadrant of the abdomen. Laboratory investigations showed increased serum total bilirubin (7.3 mg/dL; normal range, 0.3–1.1 mg/dL), direct bilirubin (2.7 mg/dL; normal range, 0–0.3 mg/dL), serum glutamic oxaloacetic transaminase (107 IU; normal range, 49 IU), serum glutamic pyruvic transaminase (175 IU; normal range, 49 IU), and serum alkaline phosphatase (1,264 IU; normal range, 270 IU) levels.

Abdominal sonography examination showed a 5 x 4 cm cystic lesion in the right lobe anterior segment of the liver with a heterogeneous echogenic interior and a ringlike pattern of calcification (Fig. 1A). The gallbladder was considered normal on sonography. There was a slight dilatation (7 mm) in the common bile duct. The intrahepatic bile duct segments were not dilated on sonography.



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Fig. 1A 46-year-old man with complaints of right upper quadrant pain, fever, icterus associated with clay-colored stools, and itching was admitted with diagnosis of obstructive cholangitis. Abdominal sonography image shows 5 x 4 cm cystic mass in right lobe anterior segment of liver with ringlike pattern of calcification (arrows).

 
Abdominal MRI and MRCP were performed for further confirmation of the sonographic diagnosis. Axial T1-weighted (TR/TE, 583/15) and T2-weighted (785/60) images revealed a 5 x 4 cm well-defined heterogeneous cystic lesion (Figs. 1B and 1C). The gallbladder also was normal on the axial T1- and T2-weighted images. The intrahepatic bile duct segments and common bile duct were not dilated on MRI.



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Fig. 1B 46-year-old man with complaints of right upper quadrant pain, fever, icterus associated with clay-colored stools, and itching was admitted with diagnosis of obstructive cholangitis. Axial T1-weighted MR image (TR/TE, 583/15) shows 5x4cm well-defined heterogeneous hypointense cystic lesion in right lobe anterior segment of liver.

 


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Fig. 1C 46-year-old man with complaints of right upper quadrant pain, fever, icterus associated with clay-colored stools, and itching was admitted with diagnosis of obstructive cholangitis. Axial T2-weighted MR image (785/60) shows 5x4cm well-defined heterogeneous hyperintense cystic lesion surrounded by hypointense rim (arrows).

 
MRCP (8,000/800; scan time, 40 sec; slice, 1/5; field of view, 250/1.3; matrix, 256 x 256) showed a cystic lesion in the right lobe anterior segment of the liver and a direct fistulous communication between a cystic lesion and the gallbladder (Fig. 1D). The common bile duct and left main hepatic duct were mildly dilated on MRCP images.



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Fig. 1D 46-year-old man with complaints of right upper quadrant pain, fever, icterus associated with clay-colored stools, and itching was admitted with diagnosis of obstructive cholangitis. MR cholangiopancreatography image (8,000/800; scan time, 40 sec; slice, 1/5; field of view, 250/1.3; matrix, 256 x 256) shows direct fistula between hydatid cyst and gallbladder (arrowheads) and mild dilatation of common bile duct and left main hepatic duct.

 
Subsequent ERCP showed a mildly dilated common bile duct without intrahepatic biliary tree dilatation. The hydatid cyst and the fistulous communication were not visualized on ERCP.

We considered hepatic hydatid cyst rupture into the gallbladder on the basis of the MRCP findings. The findings on MRCP were confirmed at surgery. Surgery also disclosed cholecystitis secondary to rupture of the hydatid cyst into the gallbladder.


Discussion
Top
Introduction
Case Report
Discussion
References
 
Hydatid disease primarily affects the liver and typically shows characteristic imaging findings. However, there are many potential local complications such as intrahepatic complications, exophytic growth, transdiaphragmatic thoracic involvement, perforation into hollow viscera, peritoneal seeding, portal vein involvement, abdominal wall invasion, and frank biliary communication, which has been reported in only 5–15% of cases [1]. It occurs in the right duct in 55–60% of cases, in the left duct in 25–30%, and rarely in the confluence or gallbladder (as in the present case) [3]. When rupture into the biliary tract occurs, the cystic fluid escapes into the biliary tract with daughter cysts discharged into the common bile duct, causing biliary colic, obstructive jaundice, and possibly liver abscess [1, 4, 5]. Our patient presented with right upper quadrant pain, fever, and jaundice.

On imaging studies, a dilated intrahepatic bile duct segment in association with an adjacent cystic lesion and dilatation of the common bile duct are generally the indirect findings of rupture of a hydatid cyst into the biliary tree. Sonography may identify the daughter cysts within the biliary tree. The fistulous communication between the hydatid cyst and biliary tract may sometimes be directly identified on different imaging studies [3]. In the present case, sonography showed a cystic lesion with a heterogeneous echogenic interior and a ringlike pattern of calcification suggestive of hepatic hydatid disease. No apparent intra- or extrahepatic biliary tree dilatation was found on sonography. Moreover, a direct communication between the cyst and gallbladder could not be seen.

MRI and MRCP are used in difficult cases, such as intrabiliary rupture, in which CT and sonography findings may be inconclusive. The MRI finding in ruptured hydatid cyst can be direct or indirect [3]. That is, the only direct sign of rupture into the biliary tree may be the visualization of the cyst wall defect or communication between the cyst and a biliary radicle [1]. In the present case, MRCP successfully identified the communication between the hydatid cyst and the gallbladder.

ERCP is the gold standard with which to confirm biliary tract involvement and may be of therapeutic value in selected cases. On ERCP, a swollen ampulla of Vater may be seen, with hydatid material protruding out. Dilated ducts with debris and daughter cysts may appear as radiolucent filling defects [3]. Although ERCP is the gold standard in the diagnosis of hydatid cyst rupture into the biliary tree, ERCP findings were negative in our patient. We believe that the negative ERCP findings were due to insufficient filling of the gallbladder with contrast medium.

In conclusion, rupture of a hepatic hydatid cyst into the gallbladder is extremely rare. Isolated rupture into the gallbladder may present with signs different from those associated with intrahepatic biliary rupture. Rupture of a cyst into the gallbladder must be included in the differential diagnosis especially in cases in which the cyst is close to the gallbladder and direct and indirect signs of intrahepatic biliary rupture are absent.


References
Top
Introduction
Case Report
Discussion
References
 

  1. Pedrosa I, Saiz A, Arrazola J, Ferreiros J, Pedrosa CS. Hydatid disease: radiologic and pathologic features and complications. RadioGraphics 2000;20 : 795–817[Abstract/Free Full Text]
  2. Lewall DB, McCorkell SJ. Rupture of echinococcal cysts: diagnosis, classification, and clinical implications. AJR1986; 146:391 –394[Abstract/Free Full Text]
  3. Kumar R, Reddy SN, Thulkar S. Intrabiliary rupture of hydatid cyst: diagnosis with MRI and hepatobiliary isotope study. Br J Radiol 2002; 75:271 –274[Abstract/Free Full Text]
  4. Marti-Bonmati L, Menor F, Ballesta A. Hydatid cyst of the liver: rupture into the biliary tree. AJR 1988;150 :1051 –1053[Abstract/Free Full Text]
  5. Kornaros SE, Aboul-Nour TA. Frank intrabiliary rupture of hydatid hepatic cyst: diagnosis and treatment. J Am Coll Surg1996; 183:466 –470[Medline]

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