首页> 外文期刊>European journal of gynaecological oncology >Borderline micropapillary serous tumor of the ovary detected during a cesarean section due to a transabdominal cervico-isthmic cerclage in a patient with congenital cervical hypoplasia: a rare case.
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Borderline micropapillary serous tumor of the ovary detected during a cesarean section due to a transabdominal cervico-isthmic cerclage in a patient with congenital cervical hypoplasia: a rare case.

机译:先天性宫颈发育不全的患者经腹子宫颈峡部环扎术在剖宫产时检测到卵巢交界性微乳头浆液性肿瘤:一种罕见的情况。

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摘要

A young woman with polycystic ovary syndrome and congenital cervical hypoplasia conceived with clomifen citrate treatment after placement of a transabdominal cervico-isthmic cerclage. Her pregnancy successfully reached term and cesarean section was performed to preserve the cerclage for the next pregnancy; when the ovaries were explored an irregular structure was detected on the left ovary. A wedge biopsy was done and the pathological assessment of the specimen was borderline micropapillary serous tumor of the ovary. The patient wanted to preserve her fertility, therefore a fertility-sparing staging surgery was performed six months after the cesarean section. There was no residual tumor in the left ovary, but there was a borderline tumor in the right ovarian biopsy specimen (frozen section was negative). Two months after staging surgery the patient conceived with IVF and delivered twins at the 33rd week of pregnancy with cesarean section. At her second cesarean section the right ovary and abdomen appeared normal on inspection, but the cerclage tape was in the endocervical canal and was thus removed. To our knowledge this is the second reported case of transabdominal cerclage tape migration into the endocervical canal. The patient is clinically disease-free 18 months after her second cesarean section. The clinical findings, treatment modalities, management and prognosis are discussed together with a literature review of a patient with a serous borderline ovarian tumor and congenital cervical hypoplasia.
机译:一名患有多囊卵巢综合征和先天性宫颈发育不全的年轻妇女在放置经腹部宫颈缺血性环扎带后,接受了柠檬酸克罗米芬治疗。她的妊娠成功地达到了足月,并进行了剖宫产以保留下一次怀孕的环扎。当探索卵巢时,在左卵巢上发现了不规则的结构。进行楔形活检,标本的病理评估为卵巢微乳头浆液性交界性肿瘤。该患者想保留自己的生育能力,因此在剖宫产后六个月进行了保留生育能力的分期手术。左卵巢中没有残留肿瘤,但右卵巢活检标本中有交界性肿瘤(冰冻切片为阴性)。分期手术后两个月,患者怀了IVF,并在妊娠第33周剖腹产时分娩了双胞胎。在她的第二胎剖腹检查时,右卵巢和腹部看起来正常,但是环扎带在子宫颈管内,因此被去除了。据我们所知,这是第二例经腹腔环扎带迁移到宫颈管内的病例。该患者在第二次剖宫产后18个月无临床疾病。讨论了患有浆液性交界性卵巢肿瘤和先天性宫颈发育不全的患者的临床发现,治疗方式,治疗和预后以及文献复习。

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