双绒毛膜双羊膜妊娠中完全性痣与正常胎儿并存:病例报告

Maryanne Mwangi, Mjahid Hassan, Wambugu Justus, Wanyonyi Shikolia
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摘要

背景:完全水样痣与正常妊娠并存是一种非常罕见的情况,据报道其发生率为 22,000-100,000 例妊娠中的 1 例。由于存在母体和胎儿并发症的风险,且最佳处理方法的数据有限,因此处理方法仍存在争议:病例介绍:一名 1+0 段孕妇在妊娠 19 周时来到母体胎儿科。超声波检查显示双胎妊娠,一个胎囊内有一个活胎,另一个胎囊内有多个囊性病变和不典型的雪暴外观,与完全性磨擦妊娠一致。臼齿妊娠的胎盘也呈低位,覆盖宫颈内口。她曾多次出现产前出血,但由于她渴望受孕,因此都得到了积极的处理。25 周时,她出现大量阴道出血和寒战。窥器检查显示有囊泡,超声波检查显示有一个活胎儿,但未观察到完全的双胎妊娠。入院后,患者出现发热和心动过速。为排除羊膜腔内感染,医生对患者进行了羊膜腔穿刺。母体血培养呈 B 群链球菌阳性,胎儿血和羊水培养无菌。胎盘组织病理学显示与急性绒毛膜羊膜炎和外周臼齿妊娠特征一致:本病例凸显了处理此类病例的难度,多次产前出血和随后的产妇败血症就是例证。多学科护理和共同决策仍是管理中不可或缺的一部分。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Complete mole coexisting with a normal fetus in a dichorionic diamniotic pregnancy: A case report
Background: Complete hydatidiform mole with a coexisting normal pregnancy is an exceptionally rareoccurrence with a reported incidence of 1 in 22,000-100,000 pregnancies. Management remainscontroversial due to the risk of maternal and fetal complications and limited data on optimalmanagement.Case presentation: A para 1 + 0 presented to the Maternal Fetal Unit at 19 weeks. Ultrasound revealed atwin pregnancy with a single live fetus in one sac and a second sac with multiple cystic lesions and atypical snow-storm appearance consistent with a complete molar pregnancy. The placenta of the molarpregnancy was also low-lying, covering the internal cervical os. She had several episodes of antepartumhemorrhage, which was managed expectantly because she was keen on conception. At 25 weeks, shepresented with copious vaginal bleeding and chills. Speculum examination revealed vesicles withultrasound revealing a single live fetus, but complete molar pregnancy was not observed. Afteradmission, the patient became febrile with tachycardia. Amniocentesis was performed to rule outintraamniotic infection in viable pregnancy. A decision was made to undertake an emergencyhysterotomy because of deteriorating maternal status, placenta previa, and breech presentation.Maternal blood culture was positive for group B Streptococcus, with fetal blood and amniotic fluid culturesbeing sterile. Histopathology of the placenta revealed features consistent with acute chorioamnionitis andperipheral molar pregnancy.Conclusion: This case highlights the difficulty in the management of such cases, as illustrated bymultiple episodes of antepartum hemorrhage and subsequent maternal sepsis. Multidisciplinary care andshared decision making remain integral to management.
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