Iorio Giuseppe Gabriele, Rovetto Marika Ylenia, Conforti Alessandro, Carbone Luigi, Vallone Roberta, Cariati Federica, Bagnulo Francesca, Di Girolamo Raffaella, La Marca Antonio, Alviggi Carlo
Department of Neuroscience, Reproductive Science and Odontostomatology, School of Medicine and Surgery, University of Naples Federico II, Naples, Italy.
Department of Obstetrics and Gynecology, Center for Fetal Care and High-Risk Pregnancy, University of Chieti, Chieti, Italy.
Front Reprod Health. 2021 Jul 6;3:704153. doi: 10.3389/frph.2021.704153. eCollection 2021.
We report a rare case of ovarian hyperstimulation syndrome (OHSS) in a 28-year-old woman with breast cancer and with a history of polycystic ovary syndrome (PCOS) despite treatment with letrozole and gonadotropin-releasing hormone agonist (GnRH-a) triggering in a GnRH antagonist (GnRH-ant) protocol without the administration of any human chorionic gonadotropin (hCG) for luteal-phase support. The patient, who underwent controlled ovarian syndrome (COS)-oocyte cryopreservation before chemotherapy, required hospitalization. Complete recovery was achieved after treatment with volume expanders, human albumin, and cabergoline. Based on our case and literature review, it is possible to establish that estradiol (E) modulation with letrozole and GnRH-a triggering does not eliminate the risk of OHSS. Furthermore, it is advisable to postpone GnRH-a to minimize the risk of OHSS after the suspension of letrozole, following menstruation or at least 7-8 days after triggering. It would be desirable to identify high-risk patients, also on a genetic basis, in order to avoid delays in oncologic treatments that could strongly impact life expectancy.
我们报告了一例罕见的卵巢过度刺激综合征(OHSS)病例,患者为一名28岁的乳腺癌女性,有多囊卵巢综合征(PCOS)病史,尽管在促性腺激素释放激素拮抗剂(GnRH-ant)方案中使用来曲唑和促性腺激素释放激素激动剂(GnRH-a)触发,且未使用任何人类绒毛膜促性腺激素(hCG)进行黄体期支持。该患者在化疗前接受了控制性卵巢刺激(COS)-卵母细胞冷冻保存,随后需要住院治疗。经使用扩容剂、人血白蛋白和卡麦角林治疗后完全康复。基于我们的病例和文献回顾,可以确定使用来曲唑和GnRH-a触发进行雌二醇(E)调节并不能消除OHSS的风险。此外,建议在月经后或触发后至少7-8天,在停用 来曲唑后推迟使用GnRH-a以将OHSS的风险降至最低。为了避免可能严重影响预期寿命的肿瘤治疗延误,还希望在基因基础上识别高危患者。