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Recurrent ovarian granulosa cell tumors: clinical and imaging features
Authors:Sung Eun Rha  Soon Nam Oh  Seung Eun Jung  Young Joon Lee  Ah Won Lee  Jae Young Byun
Affiliation:(1) Department of Radiology, Kangnam St. Mary’s Hospital, College of Medicine, The Catholic University of Korea, 505, Banpo-Dong, Seocho-Ku, Seoul, 137-040, South Korea;(2) Department of Radiology, St. Mary’s Hospital, College of Medicine, The Catholic University of Korea, #62, Youidodong, Youngdeungpo-gu, Seoul, 150-713, South Korea;(3) Department of Pathology, College of Medicine, The Catholic University of Korea, 505, Banpo-Dong, Seocho-Ku, Seoul, 137-040, South Korea
Abstract:Background Granulosa cell tumor of the ovary differs from epithelial ovarian tumors in histologic appearance, clinical course and imaging findings. The purpose of this study was to evaluate clinical and imaging features of recurrent ovarian granulosa cell tumors. Methods We performed retrospective evaluation of the medical, surgicopathologic records and CT or MR images of 11 patients with pathologically proven recurrent ovarian granulosa cell tumor. Results The first recurrence of granulosa cell tumor was diagnosed at between 4 months and 18 years after the initial surgical resection of tumor (mean; 9.7 years). Six patients relapsed after 10 years after initial diagnosis. The recurrent tumors were located in the pelvic cavity alone in three patients, extrapelvic peritoneal cavity alone in two, both pelvic and extrapelvic peritoneal cavity in three, and paraaortic retroperitoneal space in three. The imaging appearances of recurrent masses were variable ranging from solid masses to completely cystic masses. Conclusion Recurrent granulosa cell tumor is characterized by late tumor recurrence manifested as a relatively small number of discrete peritoneal or retroperitoneal masses with variable imaging appearances from solid to cystic masses.
Keywords:Granulosa cell tumor  Ovarian neoplasms  Neoplasm recurrence  Computed tomography  MR imaging
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