Fetal Intervention for Giant Chorangioma with Prenatal Ductus Arteriosus Closure: A Case Report.

IF 1.7 3区 医学 Q3 OBSTETRICS & GYNECOLOGY
Fetal Diagnosis and Therapy Pub Date : 2026-01-01 Epub Date: 2026-03-05 DOI:10.1159/000551096
Felicia V Lemoine, Natalie Neff, Sami Backley, Salima A Bhimani, Angela Bianco, Joanne Stone, Russell Miller, Anthony Johnson, Jimmy Espinoza, Rodrick C Zvavanjanja, Ramesha Papanna
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引用次数: 0

Abstract

Introduction: We present a case of spontaneous premature ductus arteriosus (DA) closure following modified interstitial laser ablation (ILA) of a giant chorangioma (GC) in a fetus with evidence of hydrops.

Case presentation: A 26-week ultrasound revealed a 10-cm GC in the posteriorly located placenta with signs of fetal hydrops, polyhydramnios, and elevated middle cerebral artery peak systolic velocity (MCA PSV) of 1.9 MoM. Preoperative fetal echocardiogram showed elevated combined cardiac output (753 mL/kg/min) without structural abnormalities. Modified ILA targeting the branches of the feeder artery with an extended-pulse technique (30 s at 40 Watts) followed by intrauterine fetal transfusion was performed without complications. On postoperative day (POD) 1, new onset of ductus venosus flow reversal was noted, which was attributed to post-procedural hemodynamics. Fetal echocardiography on POD 5 suggested constriction of DA; follow-up confirmed complete DA closure and secondary right heart dysfunction. The pregnancy was managed expectantly with at least weekly echocardiograms. Digoxin and hyperoxygenation for fetal heart failure did not change DA caliber. Acetaminophen and fluoxetine were discontinued without improvement. After an uncomplicated term cesarean delivery (indication: breech), the female neonate was discharged home on day of life 3. Currently, the child is 6 months old and healthy.

Conclusion: Modified ILA for GC followed by expectant management of associated DA closure yielded a term delivery with a favorable outcome.

胎儿介入产前动脉导管关闭治疗巨大脉管瘤1例报告。
我们报告一例自发性过早动脉导管(DA)关闭后,改进间质激光消融(ILA)的巨大脉管瘤(GC)的胎儿有证据表明积液。孕26周超声显示胎盘后部10cm GC,伴有胎儿积水、羊水过多、大脑中动脉收缩速度峰值(MCA PSV)升高1.9 MoM。术前胎儿超声心动图显示合并心输出量升高(753 ml/kg/min),无结构性异常。采用延长脉冲技术(30秒,40瓦)对喂动脉分支进行改良ILA,随后进行宫内胎儿输血,无并发症。在术后第1天(POD),注意到新的静脉导管血流逆转,这是由于手术后的血流动力学。胎儿超声心动图显示POD 5提示DA缩窄;随访证实DA完全闭合和继发性右心功能障碍。通过至少每周一次的超声心动图对妊娠进行了预期管理。地高辛和高氧治疗胎儿心力衰竭没有改变DA口径。停用对乙酰氨基酚和氟西汀无改善。在一次无并发症的足月剖宫产(指征:臀位)后,女婴在出生第3天出院回家。目前,孩子6个月大,身体健康。结论改良的腹腔内瘘治疗GC,并辅以相关DA闭合的预期治疗,可获得良好的预后。
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来源期刊
Fetal Diagnosis and Therapy
Fetal Diagnosis and Therapy 医学-妇产科学
CiteScore
4.70
自引率
9.10%
发文量
48
审稿时长
6-12 weeks
期刊介绍: The first journal to focus on the fetus as a patient, ''Fetal Diagnosis and Therapy'' provides a wide range of biomedical specialists with a single source of reports encompassing the common discipline of fetal medicine.
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