Pregnancy, Triplet

怀孕,三元组
  • 文章类型: Journal Article
    背景:临床实践中多胎妊娠率的增加与辅助生殖技术(ART)有关。鉴于二胎羊膜三胎(DCTA)三胎妊娠的高风险,将DCTA三胎妊娠减少为双胎或单胎妊娠通常是有益的。
    方法:本文报道了两例由两次胚泡移植导致的DCTA三胎妊娠。鉴于单绒毛膜双胎(MCDA)双胎妊娠双胎输血综合征(TTTS)等并发症的高风险,患者有强烈的愿望,以保持二氧化羊膜(DCDA)双胞胎。在两种情况下都进行了多胎妊娠减少(MFPR),以通过减少一个MCDA双胞胎来继续DCDA双胞胎的妊娠。这份报告中的两位孕妇最终在37周时生下了健康的双胞胎。
    结论:对于多胎妊娠但强烈希望保留DCDA双胞胎的不育夫妇,我们的报告提示,根据临床可操作性和手术难度评估,将DCTA三胞胎减少至DCDA双胎妊娠可能是一种选择.
    BACKGROUND: The increase in the rate of multiple pregnancies in clinical practice is associated with assisted reproductive technology (ART). Given the high risk of dichorionic triamniotic (DCTA) triplet pregnancies, reducing DCTA triplet pregnancies to twin or singleton pregnancies is often beneficial.
    METHODS: This article reports on two cases of DCTA triplet pregnancies resulting from two blastocyst transfers. Given the high risk of complications such as twin-to-twin transfusion syndrome (TTTS) in monochorionic diamniotic (MCDA) twin pregnancies, patients have a strong desire to preserve the dichorionic diamniotic (DCDA) twins. Multifetal pregnancy reduction (MFPR) was performed in both cases to continue the pregnancy with DCDA twins by reducing one of the MCDA twins. Both of the pregnant women in this report eventually gave birth to healthy twins at 37 weeks.
    CONCLUSIONS: For infertile couples with multiple pregnancies but with a strong desire to remain the DCDA twins, our report suggests that reducing DCTA triplets to DCDA twin pregnancies may be an option based on clinical operability and assessment of surgical difficulty.
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  • 文章类型: Case Reports
    目的:人工生殖技术后的单绒毛膜羊膜(MCTA)三胎妊娠并不常见。我们报告了一个案例,其中两个转移的胚胎之一分化为MCTA三联体。本研究旨在探讨MCTA三胎妊娠的潜在因素。
    方法:一名39岁的女性接受了第二次冷冻胚胎移植,并带有孵化的囊胚,这导致在超声检查中检测到MCTA三联。她在妊娠32周时剖腹产,导致三个活生生的男婴出生。回顾了她的病史和体外受精治疗,以确定潜在的原因。
    结论:MCTA三胎妊娠的病因仍然是多因素的。在本案中,延长体外培养至胚泡期和内细胞团分裂是潜在的促成因素。需要进一步的研究来充分了解MCTA三胎妊娠的复杂性。
    OBJECTIVE: Monochorionic-triamniotic (MCTA) triplet pregnancies following artificial reproductive technologies are uncommon. We report a case in which one of two transferred embryos differentiated into an MCTA triplet. This study aimed to investigate the potential factors contributing to MCTA triplet pregnancy.
    METHODS: A 39-year-old woman underwent her second frozen embryo transfer with hatching blastocysts, which resulted in the detection of an MCTA triplet on ultrasonography. She delivered by cesarean section at 32 weeks of gestation, resulting in the birth of three live male infants. Her medical history and in vitro fertilization treatment were reviewed to identify potential causes.
    CONCLUSIONS: The etiology of MCTA triplet pregnancy remains multifactorial. In the presented case, prolonged in vitro culture to the blastocyst stage and inner cell mass splitting were potential contributing factors. Further research is needed to fully understand the complexity of MCTA triplet pregnancy.
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  • 文章类型: Case Reports
    多胎妊娠与重要的产妇有关,胎儿,和新生儿风险,包括早产,低出生体重,先兆子痫,贫血,产后出血,宫内生长受限,新生儿发病率,新生儿和婴儿死亡率上升。辅助生殖技术(ART)治疗应优先考虑减少此类事件的努力,抵制患者在每次移植时移植多个胚胎的需求,以提高成功率。扩展文化,胚胎选择,单囊胚移植可以降低高阶多胎妊娠的风险。有趣的是,选择性单胚胎移植(eSET)大大减少,但并不能完全消除,多重妊娠的可能性。单卵孪生(MZT)的发生导致同卵双胞胎。与自然受孕相比,在接受体外受精(IVF)的女性中更为普遍。事实上,据报道,体外受精和自然受孕中单卵双胞胎的风险分别为1.7%和0.4%,分别。在IVF中可能增加MZT风险的因素是多胚胎移植,显微操作,和扩展的体外培养。确定绒毛膜和羊膜性对于评估妊娠早期超声检查中的多胎妊娠至关重要。受精后3天内胚胎分裂导致双生子,而单绒毛膜双胞胎发生在受精后4到8天之间分裂时。通过在自然怀孕中进行的观察来建议这些时间。在艺术中,有单胚胎移植(SET)的二胎双胞胎的证据.这里,我们报告了一例在我们中心发生单个胚泡移植后的二胎性羊膜三胞胎。据我们所知,这是迄今为止记录的第一个案例。
    Multiple pregnancies are associated with significant maternal, fetal, and neonatal risks, including prematurity, low birth weight, pre-eclampsia, anemia, postpartum hemorrhage, intrauterine growth restriction, neonatal morbidity, and increased neonatal and infant mortality rates. Assisted reproductive technology (ART) treatments should prioritize efforts to reduce such events, resisting patient demand for the transfer of multiple embryos at each transfer to increase success rates. Extended culture, embryo selection, and single blastocyst transfer can mitigate the risk of high-order multiple pregnancies. Intriguingly, elective single-embryo transfer (eSET) greatly reduces, but does not completely eliminate, the likelihood of multiple gestations. The occurrence of monozygotic twinning (MZT) gives rise to identical twins. It is more prevalent in women undergoing in vitro fertilization (IVF) compared with natural conception. In fact, the reported risks of monozygotic twinning in IVF and natural conception are 1.7 and 0.4%, respectively. The factors suspected to increase the risk of MZT in IVF are multiple embryo transfer, micromanipulation, and extended in vitro culture. Determining chorionicity and amnionicity is crucial in the assessment of multiple pregnancies during the first-trimester ultrasound examination. Dichorionic twins result from embryo splitting within 3 days after fertilization, while monochorionic twins occur when the splitting takes place between 4 and 8 days after fertilization. These timings are suggested by observations carried out in natural pregnancies. In ART, there is evidence of dichorionic twins derived from single embryo transfer (SET). Here, we report a case of dichorionic diamniotic triplets after a single blastocyst transfer occurred in our center. To our knowledge, this is the first case documented so far.
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  • 文章类型: Case Reports
    先天性皮肤发育不全(ACC)是一种罕见的先天性局部皮肤缺损,主要在新生儿或婴儿时期被诊断出来。ACC5型通常累及躯干或四肢,并伴有胎儿纸草质(FP)或胎盘梗塞。这种罕见类型ACC的病因和发病机制尚不清楚。在这种情况下,我们报告了明确病因的ACC5型。
    我们报告了1例ACC5型早产儿,出生时发现弥漫性双侧腿部病变。他是通过体外受精从二胎三胎怀孕中减少的二胎双胞胎的第一个婴儿。与受影响的婴儿胎盘并列发现了胎儿纸莎草质。住院37天后,他的腿部病变在支持治疗下成功上皮化。他定期到皮肤科诊所进行疤痕护理,并显示出正常的发育,没有运动限制。
    这里,我们介绍了患有ACC5型的早产儿,以及受影响的婴儿的人工减少的单绒毛膜共生体的胎盘病理与胎儿纸草质。我们建议在三胞胎中多胎妊娠减少(MFPR)的谨慎决定,将ACC5型作为MFPR的不良结局。
    Aplasia cutis congenita (ACC) is a rare congenital localized skin defect that is mostly diagnosed in the newborn or infant period. ACC type 5 often involves the trunk or extremities accompanied by fetus papyraceous (FP) or placental infarcts. The etiology and pathogenesis of this rare type of ACC are not well known. In this case, we report an ACC type 5 with a definite etiology.
    We report a preterm infant with ACC type 5, with diffuse bilateral leg lesions found at birth. He was the first baby of dichorionic twin after reduction from a dichorionic triplet pregnancy conceived through in vitro fertilization. A fetus papyraceous was found in juxtaposition with the affected baby`s placenta. After 37 days of hospitalization, his leg lesions were successfully epithelized with supportive care. He is regularly visiting the Dermatology clinic for scar care and shows normal development without motor limitation.
    Herein, we present a preterm infant with ACC type 5 and the placental pathology with fetus papyraceous of the artificially reduced monochorionic co-twin of the affected infant. We suggest a precautious decision in multifetal pregnancy reduction (MFPR) in dichorionic triplets, presenting ACC type 5 as an adverse outcome of MFPR.
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  • 文章类型: Case Reports
    暂无摘要。
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  • 文章类型: Case Reports
    BACKGROUND: Monochorionic diamniotic triplet pregnancies are rare. Twin reversed arterial perfusion sequence in monochorionic triplet pregnancies is extremely rare, and it is associated with high perinatal morbidity and mortality rates in the \"pump fetus.\"
    METHODS: We reported a case of monochorionic diamniotic triplet pregnancy with twin reversed arterial perfusion sequence, including two acardiac fetuses sharing a single amniotic sac and a normal fetus in another amniotic sac. Due to rapid growth of the acardiac fetuses, intrafetal laser therapy was performed in both of them under ultrasound guidance at 15 weeks +5 days. Subsequently, regular and careful antenatal care including fetal ultrasonography and doppler and fetal echocardiography was conducted. At 37 weeks +4 days, a healthy female baby weighing 2510 g was delivered. The baby was followed up and now at 11 months old is in good health.
    CONCLUSIONS: Twin reversed arterial perfusion sequence in monochorionic triplet pregnancy should be diagnosed early by ultrasound imaging during pregnancy. Individualized management should be based on clinical conditions to improve the perinatal outcome of the pump twin. Intrafetal laser therapy could be an alternative procedure when intrauterine intervention is required.
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  • 文章类型: Case Reports
    背景:2019年冠状病毒病(COVID-19),在世界各地蔓延的全球流行病,是由严重急性呼吸道综合症冠状病毒2(SARS-CoV-2)引起的。鉴于关于这种病毒对怀孕的表现和潜在影响的科学证据有限,我们决定报告这个案子。
    方法:患者是一名38岁的伊朗妇女,有三胎妊娠和原发性不孕症病史,以及甲状腺功能减退和妊娠期糖尿病。由于肝酶升高,她在胎龄29周零2天时住院,最后,根据妊娠胆汁淤积的可能诊断,她接受了熊去氧胆酸治疗。住院的第一天,进行了超声检查,这表明所有三个胎儿的生物物理评分和羊水都是正常的,两个胎儿的多普勒表现正常,一个胎儿的脐动脉阻力增加(搏动指数[PI]>95%)。住院第4天,她发烧了,咳嗽和肌痛,她的COVID-19检测呈阳性。尽管产妇症状轻微,其中两个胎儿发生胎盘功能不全,导致脐动脉舒张末期血流缺失的快速发展。最后,6天后,患者因胎盘功能不全迅速恶化和其中2例胎儿的生物物理评分下降而接受了剖宫产.鼻咽拭子COVID-19测试对第一个和第三个婴儿呈阴性,对第二个婴儿呈阳性。第一个和第三个婴儿在出生后3天和13天死亡,分别,由于白肺塌陷和败血症。第二个婴儿在良好的情况下出院。产妇在剖宫产术后3天出院。她出院时没有发烧,一般情况也很好。
    结论:这是一个复杂的三胎妊娠,其中,在母亲感染COVID-19后,尽管母亲症状轻微,加剧的胎盘功能不全发生在两个胎儿,第三个胎儿出生后COVID-19检测呈阳性。因此,在妊娠感染COVID-19的情况下,除了管理母亲,医生似乎也应该特别注意急性胎盘功能不全和随后的胎儿缺氧的可能性,以及垂直传播的可能性。
    BACKGROUND: Coronavirus disease 2019 (COVID-19), the global pandemic that has spread throughout the world, is caused by severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2). Given the limited scientific evidence on the manifestations and potential impact of this virus on pregnancy, we decided to report this case.
    METHODS: The patient was a 38 year-old Iranian woman with a triplet pregnancy and a history of primary infertility, as well as hypothyroidism and gestational diabetes. She was hospitalized at 29 weeks and 2 days gestational age due to elevated liver enzymes, and finally, based on a probable diagnosis of gestational cholestasis, she was treated with ursodeoxycholic acid. On the first day of hospitalization, sonography was performed, which showed that biophysical scores and amniotic fluid were normal in all three fetuses, with normal Doppler findings in two fetuses and increased umbilical artery resistance (pulsatility index [PI] > 95%) in one fetus. On day 4 of hospitalization, she developed fever, cough and myalgia, and her COVID-19 test was positive. Despite mild maternal symptoms, exacerbated placental insufficiency occurred in two of the fetuses leading to the rapid development of absent umbilical artery end-diastolic flow. Finally, 6 days later, the patient underwent cesarean section due to rapid exacerbation of placental insufficiency and declining biophysical score in two of the fetuses. Nasopharyngeal swab COVID-19 tests were negative for the first and third babies and positive for the second baby. The first and third babies died 3 and 13 days after birth, respectively, due to collapsed white lung and sepsis. The second baby was discharged in good general condition. The mother was discharged 3 days after cesarean section. She had no fever at the time of discharge and was also in good general condition.
    CONCLUSIONS: This was a complicated triplet pregnancy, in which, after maternal infection with COVID-19, despite mild maternal symptoms, exacerbated placental insufficiency occurred in two of the fetuses, and the third fetus had a positive COVID-19 test after birth. Therefore, in cases of pregnancy with COVID-19 infection, in addition to managing the mother, it seems that physicians would be wise to also give special attention to the possibility of acute placental insufficiency and subsequent fetal hypoxia, and also the probability of vertical transmission.
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  • 文章类型: Case Reports
    背景:连体婴是单绒毛膜妊娠的一种罕见并发症,也是自发性三胞胎妊娠的一种极为罕见的情况。我们报告了一例自发性单绒毛膜三胎妊娠中的连体双胞胎。这对双胞胎可能患有双胎贫血-红细胞增多症,据报道这是极为罕见的。
    方法:一名26岁女性,4年前有浸润性葡萄胎的产科病史。
    方法:我们最初误诊为妊娠10周时患有单绒毛膜三胎羊膜三胎。然而,我们在妊娠12周时确认了合并双胎和单绒毛膜双胎的三胎妊娠,并将其分类为脐眼.
    方法:当女性决定继续怀孕时,进行了定期和仔细的产前护理。
    结果:出乎意料的是,她在3周后死产,在妊娠15周时不得不终止妊娠.流产后,在诱导的胎儿中证实了脐的诊断。此外,这对连体双胞胎的肤色不同:一个是多姿多彩的,另一个脸色苍白。此外,父母同意检查胎儿的染色体,结果正常.
    结论:三胎和单胎三胎妊娠的预后比三胎三胎妊娠差。手术是连体双胞胎的主要治疗方法;然而,三胞胎中的大多数连体双胞胎无法存活,包括omphalopagus双胞胎.连体双胞胎可能患有双胎贫血-红细胞增多症,这可能不能被诊断为子宫内。经阴道探头和三维超声可能有助于明确妊娠早期的诊断。
    BACKGROUND: Conjoined twins are a rare complication of monochorionic pregnancies and an extremely rare condition in spontaneous triplet pregnancies. We report a case of conjoined twins in a spontaneous monochorionic triplet pregnancy. The conjoined twins might have suffered from twin anemia-polycythemia sequence, which was reported to be extremely rare.
    METHODS: A 26-year-old woman conceived spontaneously with an obstetric history of invasive mole 4 years ago.
    METHODS: We initially misdiagnosed her as having monochorionic triamniotic triplets at 10 weeks of gestation. However, we confirmed conjoint twins with the monochorionic diamniotic triplet pregnancy at 12 weeks of gestation and classified them as omphalopagus.
    METHODS: As the woman decided to continue the pregnancy, regular and careful antenatal care was conducted.
    RESULTS: Unexpectedly, she had a stillbirth 3 weeks later and had to terminate the pregnancy at 15 weeks of gestation. After abortion, the diagnosis of omphalopagus was confirmed in the induced fetuses. Moreover, the skin colors of the conjoined twins were different: one was plethoric, and the other was pale. Additionally, the parents agreed to examine the chromosome of the fetuses, and the results were normal.
    CONCLUSIONS: Dichorionic triplet and monochorionic triplet pregnancies have a poorer prognosis than trichorionic triplet pregnancies. Surgery is the main therapy for conjoined twins; however, most conjoined twins in triplet pregnancies cannot survive, including omphalopagus twins. The conjoined twins may have suffered from twin anemia-polycythemia sequence, which could probably not be diagnosed intrauterine. Transvaginal probe and 3-dimensional ultrasound may be helpful for clarifying the diagnosis in early pregnancy.
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  • 文章类型: Case Reports
    Delayed delivery is designed to allow the remaining fetus(es) to develop after premature expulsion of the first twin in the second trimester of pregnancy. This decision is aimed to allow the remaining fetus(es) to reach full fetal growth. We here report a clinical case of delayed delivery in a patient with triple pregnancy in whom the time between the expulsion of the first twin and the birth of the third twin was 10 weeks. The purpose of this study was to highlight the benefit and indications for delayed delivery.
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  • 文章类型: Case Reports
    Ovarian hyperstimulation syndrome (OHSS) is a serious complication of ovarian stimulation. Herein, we report a rare case of strangulated internal hernia in a woman with severe OHSS following ovulation induction. A delay in the diagnosis and management of acute abdominal pain can lead to serious problems. The aim of this case report was to highlight the diagnostic difficulties of abdominal pain in women with OHSS, and emphasize the positive effects of imaging and a timely differential diagnosis in clinical practice.
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