hepatobiliary cystadenoma
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2021 ◽  
Vol 8 ◽  
Author(s):  
Yan Tang ◽  
Chenyu Wang ◽  
Shunjun Fu ◽  
Ting Li ◽  
Guolin He

Background: Biliary cystadenomas are rare cystic tumors of the bile duct system that are mostly benign but also have the possibility of malignant transformation. Biliary cystadenomas mostly occur in the intrahepatic bile ducts and are more common in middle-aged women. Due to non-specific radiology, preoperative diagnosis is difficult and is usually performed by postoperative pathology. Complete resection is the best treatment option, and the postoperative prognosis is good.Case Description: This study reports a case of a patient with biliary cystadenoma who was diagnosed with simultaneous chronic hepatitis B and colon (hepatic flexure) adenomatous polyps. The patient presented to the doctor because of abdominal pain, and a blood test showed hepatitis B. Computed tomography revealed both right liver and colonic lesions. Colonoscopy revealed polyps, and the postoperative pathological diagnosis was adenomatous polyps. Laparoscopic resection of the right liver tumor was performed, and it was diagnosed as hepatobiliary cystadenoma by postoperative pathological analysis combined with immunohistochemistry.Conclusion: In patients with chronic hepatitis, the shape of biliary cystadenoma may not be very typical, and it is necessary to combine this with immunohistochemistry for diagnosis. When multiple lesions are detected in the painful area, the diagnosis of each lesion and its treatment sequence are worthy of consideration. Under normal circumstances, the prognosis of biliary cystadenoma is good; however, in patients with chronic hepatitis B, more cases need to be observed for verification.


2020 ◽  
Vol 4 (2) ◽  
Author(s):  
Sunil Vitthalrao Jagtap

Hepatobiliary cystadenoma is a rare benign cystic tumor of the liver. These are predominantly located in right hepatic lobe. A 45 year old female presented with abdominal pain, epigastric discomfort, fever and vomiting. On radiological evaluation USG showed large multiloculated cystic mass in right lobe of liver. Contrast Enhanced CT examination exhibited exophytically growing multiloculated cytic lesion with differential content and peripheral capsular and central enhancement with imaging diagnosis of hydatid cyst was given. The surgical excision of hepatic cyst was done. On histopathology reported as mucinous cystadenoma of liver with mesenchymal stroma. We are presenting this case for its rarity, clinical, radiological and histopathological findings.


2018 ◽  
Vol 110 ◽  
pp. 598-598
Author(s):  
Héctor-Enrique Lozano-Ramírez ◽  
Pablo Ramírez-Mendoza ◽  
José Luis Beristain-Hernández

Author(s):  
Brian Quigley ◽  
Michelle D. Reid ◽  
Burcin Pehlivanoglu ◽  
Malcolm H. Squires ◽  
Shishir Maithel ◽  
...  

2016 ◽  
Vol 111 ◽  
pp. S528
Author(s):  
Moaz Sial ◽  
Nitin Sardana ◽  
Tadahiro Uemura ◽  
Abhijit Kulkarni

Medicine ◽  
2015 ◽  
Vol 94 (3) ◽  
pp. e400 ◽  
Author(s):  
En-Liang Li ◽  
Shi-Dai Shi ◽  
Yong Huang ◽  
Lin-Quan Wu

Pathology ◽  
2014 ◽  
Vol 46 ◽  
pp. S67
Author(s):  
Melissa Holmes ◽  
John Ciciulla

2013 ◽  
Vol 95 (7) ◽  
pp. 507-510 ◽  
Author(s):  
JML Williamson ◽  
JR Rees ◽  
I Pope ◽  
A Strickland

Introduction Hepatobiliary cystadenomas are rare cystic tumours that can arise from any portion of the biliary tract but most commonly develop intrahepatically. They typically cause non-specific symptoms and are often detected incidentally. Cystadenomas can be mistaken for simple hepatic cysts on radiological imaging, which leads to inadequate treatment. Hepatobiliary cystadenomas have a malignant predisposition and a high recurrence rate. Complete excision including hepatic resection is therefore generally recommended. Methods Three cases of hepatobiliary cystadenoma were identified at one unit over a six-month period. Their clinical details and management are reported. Results Three female patients are described aged 25, 37 and 73 years. One patient presented because of recurrent infection, one presented because of pressure related symptoms and one lesion was identified incidentally. All patients were investigated by ultrasonography and computed tomography (CT), two additionally had magnetic resonance imaging (MRI) and one had a liver biopsy. The tumours were 4–16cm in size and all lesions were excised by non-anatomical, parenchyma sparing resections. Histology revealed mixed epithelium with underlying ovarian-like stroma. Conclusions The management of hepatic cystadenomas as well as operative and pathological findings are discussed. Preoperative ultrasonography, CT and MRI is recommended, and early referral for specialist hepatobiliary review is advised. Operative resection is also recommended and complete excision was achieved in these cases. This strategy is supported by the current literature and recurrence has been shown to be unlikely.


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