医学
畸胎瘤
未成熟畸胎瘤
卵巢畸胎瘤
生殖细胞肿瘤
入射(几何)
外科
化疗
光学
物理
作者
Livia Zagamé,Patricia Pautier,Pierre Duvillard,Damienne Castaigne,Catherine Patte,Catherine Lhommé
标识
DOI:10.1097/01.aog.0000231686.94924.41
摘要
In Brief OBJECTIVE: To analyze a series of occurrences of growing teratoma syndrome after ovarian germ cell tumors. METHODS: We analyzed a database containing 103 patients affected by pure or mixed ovarian immature teratoma. RESULTS: We report 12 patients fulfilling growing teratoma syndrome criteria (incidence 12%). The median interval between the diagnosis of ovarian immature teratoma and growing teratoma syndrome was 9 months (range 4–55). Growing teratoma syndrome was revealed by radiological examinations in nine cases (75%). In all cases but one, growing teratoma syndrome occurred in the site involved by the primary tumor. The peritoneum was the first site involved (10 cases, 83%). A complete surgical resection of the growing teratoma syndrome was done in eight cases. The median follow-up was 144 months. Four patients presented a late growing teratoma syndrome recurrence after treatment (second event), more than 5 years after the initial diagnosis, and 14 years later for one patient. All patients but one (lost to follow-up) were still alive at the end of the study. CONCLUSION: The treatment of growing teratoma syndrome consists of the surgical resection of the tumor, as completely as possible. Because of the possibility of very late recurrence of growing teratoma syndrome, a prolonged follow-up of patients treated for ovarian immature teratoma is mandatory. LEVEL OF EVIDENCE: II-3 We report 12 patients fulfilling growing teratoma syndrome criteria out of about 103 patients affected by pure or mixed ovarian immature teratoma (incidence 12%).
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