Bifulco G, Mandato V D, Giampaolino P, Nappi C, De Cecio R, Insabato L, Tarsitano F, Mignogna C
Department of Gynecology and Obstetrics, University of Naples Federico II, Naples, Italy.
Anticancer Res. 2008 Jul-Aug;28(4C):2309-15.
Primary retroperitoneal mucinous cystadenoma is a rare tumor only 48 cases have been reported in international literature. Patients affected by primary retroperitoneal mucinous cystadenoma/cystadenocarcinoma ranged in age from 17 to 86 years (median, 42.3 years) and the size of the cystis ranged from 5 to 35 cm (median, 16.1 cm). There is no unanimous opinion on the genesis of these tumors and, due to their extreme rarity, its histogenesis, biological behavior and the optimal management strategy remain at a speculative level.
We report the case of a huge borderline primary retroperitoneal mucinous cystadenoma (24 x 25 cm) in a 35-year-old woman and the strategies adopted for the diagnosis and surgical management.
Primary mucinous cystic tumor of the retroperitoneum was correctly diagnosed only at the time of surgery. As well as in the majority of cases reported in the literature, preoperative investigations were not able to give information about the tumor site. In spite of the short follow-up (two years), the patient's favorable course supports the hypothesis that primary retroperitoneal mucinous cystadenoma may be treated in the same manner as a primary ovarian tumor of the same grade and comparable stage.
原发性腹膜后黏液性囊腺瘤是一种罕见肿瘤,国际文献仅报道了48例。原发性腹膜后黏液性囊腺瘤/囊腺癌患者的年龄在17至86岁之间(中位数为42.3岁),囊肿大小在5至35厘米之间(中位数为16.1厘米)。对于这些肿瘤的起源尚无一致意见,由于其极为罕见,其组织发生、生物学行为及最佳治疗策略仍处于推测阶段。
我们报告一例35岁女性巨大的临界性原发性腹膜后黏液性囊腺瘤(24×25厘米)病例以及所采用的诊断和手术治疗策略。
原发性腹膜后黏液性肿瘤仅在手术时得以正确诊断。与文献报道的大多数病例一样,术前检查无法提供有关肿瘤部位的信息。尽管随访时间较短(两年),但患者的良好病程支持以下假说:原发性腹膜后黏液性囊腺瘤的治疗方式可与相同分级和相似分期的原发性卵巢肿瘤相同。