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Primary Retroperitoneal Mucinous Cystadenoma
Seok Youn Lee1, Weon Cheol Han2
1Department of Surgery, Wonkwang University Sanbon Hospital, Wonkwang University School of Medicine, Iksan, Korea.
Annals of Coloproctology
|March 11, 2016
Summary
Primary retroperitoneal mucinous cystic tumors are rare but can be diagnosed and treated. This case highlights successful laparoscopic resection of a benign mucinous cystadenoma.
Area of Science:
- Gastroenterology
- Surgical Oncology
- Pathology
Background:
- Mucinous cystadenomas and cystadenocarcinomas are common ovarian tumors.
- Primary retroperitoneal mucinous cystic tumors are exceptionally rare with uncertain histogenesis.
- Preoperative diagnosis is challenging, and delayed treatment can lead to fatal complications.
Purpose of the Study:
- To report a rare case of primary retroperitoneal mucinous cystadenoma.
- To emphasize the diagnostic challenges and successful laparoscopic management.
- To contribute to the understanding of retroperitoneal cystic neoplasms.
Main Methods:
- Case presentation of a 31-year-old woman with abdominal symptoms.
- Computed tomography (CT) scan for retroperitoneal mass identification.
- Laparoscopic resection of the cystic mass.
- Histopathological examination for definitive diagnosis.
Main Results:
- CT revealed a significant retroperitoneal cystic mass.
- Laparoscopic surgery was performed successfully.
- Histopathology confirmed a primary retroperitoneal mucinous cystadenoma.
- The patient experienced an uneventful recovery and was discharged on postoperative day 5.
Conclusions:
- Primary retroperitoneal mucinous cystadenoma is a rare entity requiring accurate diagnosis.
- Laparoscopic resection is a viable and effective treatment option.
- Early diagnosis and surgical intervention are crucial for favorable patient outcomes.