Double Myelomeningocele Repair by Fetal Surgery with a Single Micro-Hysterotomy.

IF 0.9 4区 医学 Q4 CLINICAL NEUROLOGY Pediatric Neurosurgery Pub Date : 2024-01-01 Epub Date: 2024-02-09 DOI:10.1159/000537723
Felipe Chavelas-Ochoa, Ma de la Luz Bermúdez-Rojas, Virginia Medina-Jiménez, Antonio Helue-Mena, Savino Gil-Pugliese, Ivan Gutiérrez-Gómez, Miguel Martínez-Rodríguez, Carmen Julia Gaona-Tapia, Rosa Villalobos-Gómez, Karla Aguilar-Vidales, Rogelio Cruz-Martínez
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Abstract

Introduction: Open spina bifida (OSB) is the most common congenital anomaly of the central nervous system. It is associated with severe neurodevelopmental delay, motor impairment, hydrocephalus, and bowel and bladder dysfunction. In selected cases, intrauterine spina bifida repair has been shown to improve neonatal outcomes. Rarely, the spine can have a double defect compromising two different segments and there is a lack of evidence on the feasibility and benefits of intrauterine repair in these cases.

Case presentation: We present a case with both cervicothoracic and lumbosacral myelomeningocele, Arnold-Chiari malformation type II and bilateral ventriculomegaly, that was treated successfully at 25 weeks with open micro-neurosurgery. Double myelomeningocele was successfully treated through a single 2-cm micro-hysterotomy, by performing external versions to sequentially expose and repair both defects. Weekly postoperative follow-up showed no progression of ventriculomegaly or complications attributable to the procedure. Preterm rupture of membranes prompted a conventional cesarean delivery at 32 weeks of gestation. Neurodevelopmental outcome at 20 months was within normal ranges, having achieved ambulation without orthopedic support and with no need for ventriculoperitoneal shunting.

Conclusion: This report demonstrates for the first time the feasibility of double OSB repair through a single 2-cm micro-hysterotomy, suggesting that selected isolated cases of double myelomeningocele could be candidates for fetal intervention. Further prospective studies should be carried out to assess the potential benefit of double OSB intrauterine open repair.

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通过胎儿手术进行双脊髓脊膜膨出修补术,只需进行一次微切口。
简介开放性脊柱裂(OSB)是中枢神经系统最常见的先天性畸形。它与严重的神经发育迟缓、运动障碍、脑积水、肠道和膀胱功能障碍有关。在某些情况下,宫内脊柱裂修复术可改善新生儿预后。罕见的是,脊柱可能有双重缺陷,损害两个不同的节段,对于这些病例,宫内修复的可行性和益处尚缺乏证据:我们介绍了一例同时患有颈胸椎和腰骶部脊髓膜膨出、阿诺德-卡氏畸形II型和双侧脑室肥大的病例,该病例在25周时成功接受了开放式显微神经外科手术治疗。通过一次2厘米的显微子宫切除术,成功治疗了双侧脊髓脑膜膨出,术中进行了外翻,依次暴露并修复了两个缺损。术后每周随访显示,脑室肿大没有恶化,也没有出现手术并发症。胎膜早破促使她在妊娠32周时进行了常规剖宫产。20个月时,患者的神经发育结果在正常范围内,无需矫形器支持即可行走,也无需进行脑室腹腔分流:本报告首次证明了通过单个 2 厘米微切口进行双侧 OSB 修补术的可行性,表明经过选择的双侧脊髓膜膨出孤立病例可作为胎儿干预的候选病例。应进一步开展前瞻性研究,以评估双OSB宫内开放修补术的潜在益处。
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来源期刊
Pediatric Neurosurgery
Pediatric Neurosurgery 医学-临床神经学
CiteScore
1.30
自引率
0.00%
发文量
45
审稿时长
>12 weeks
期刊介绍: Articles in ''Pediatric Neurosurgery'' strives to publish new information and observations in pediatric neurosurgery and the allied fields of neurology, neuroradiology and neuropathology as they relate to the etiology of neurologic diseases and the operative care of affected patients. In addition to experimental and clinical studies, the journal presents critical reviews which provide the reader with an update on selected topics as well as case histories and reports on advances in methodology and technique. This thought-provoking focus encourages dissemination of information from neurosurgeons and neuroscientists around the world that will be of interest to clinicians and researchers concerned with pediatric, congenital, and developmental diseases of the nervous system.
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