Abstract
Primary mucinous cystadenomas of the retroperitoneum is extremely rare, and its histogenesis and biological behavior is unclear. Most authors suggested that it develops via mucinous metaplasia in a pre-existing mesothelium-lined cyst. We report here on a case of a 47-year-old Korean woman with primary retroperitoneal mucinous cystadenoma. Although the tumor was detected by ultrasound and computed tomography (CT), a preoperative diagnosis could not be established. The cystic tumor was successfully removed by laparoscopic surgery and microscopic examination revealed a mucinous cystadenoma. It had an ovarian stromal-like aspect and a lining of monolayer cuboidal epithelium; the tumor measured 5.0×5.0×3.5cm in size.
References
1. Min BW, Kim JM, Um JW, Lee ES, Son GS, Kim SJ, et al. The first case of primary retroperitoneal mucinous cystadenoma in Korea: a case report. Korean J Intern Med. 2004. 19:282–284.
2. Williams PP, Gall SA, Prem KA. Ectopic mucinous cystadenoma. A case report. Obstet Gynecol. 1971. 38:831–837.
3. Lauchlan SC. Metaplasias and neoplasias of Mullerian epithelium. Histopathology. 1984. 8:543–557.
4. Banerjee R, Gough J. Cystic mucinous tumours of the mesentery and retroperitoneum: report of three cases. Histopathology. 1988. 12:527–532.
5. Afriat R, Mechet I, Rachedi N, Michenet P, Bardaxoglou E, Grossetti D. Primary retroperitoneal mucinous cystadenoma: a case treated by celioscopic surgery. J Chir (Paris). 1995. 132:67–69.