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母体I型阿诺德-奇亚里畸形与脊髓空洞症:分娩管理困境

Maternal Arnold-Chiari type I malformation and syringomyelia: a labor management dilemma.

作者信息

Parker Jason D, Broberg Jeffrey C, Napolitano Peter G

机构信息

Division of Maternal-Fetal Medicine, Madigan Army Medical Center, Tacoma, Washington, USA.

出版信息

Am J Perinatol. 2002 Nov;19(8):445-50. doi: 10.1055/s-2002-36841.

Abstract

Arnold-Chiari type I malformations consists of elongation of the cerebellar tonsils with their displacement below the foramen magnum. Syringomyelia is an associated cyst that accumulates cerebrospinal fluid in the cord that can impinge on local nerve fibers. Pregnant women with either of these disorders are of special concern due to the potential risk of brain stem herniation and or spinal column compression from physiological changes that occur during labor. We present two cases. The first case is a patient with syringomyelia who was admitted in labor with worsening peripheral neurological symptoms. Epidural anesthesia was placed and she underwent an uncomplicated cesarean delivery with resolution of her symptoms postpartum. The second case is a patient with an Arnold-Chiari type I malformation and syringomyelia who presented in labor. The patient had an epidural placed and was allowed to progress to complete dilation and effacement at +2 station. She underwent a successful operative vaginal delivery without voluntary maternal expulsive efforts. Both patients had uncomplicated postpartum courses. Although these are rare disorders with significant potential morbidity, labor can be managed by either mode of delivery with careful patient selection. We caution that this review has insufficient numbers of patients to address the safety and efficacy of either delivery mode but rather focuses on alternatives for delivery. This report is the first to document a case of a patient with an Arnold-Chiari malformation and syringomyelia successfully managed in labor with a vaginal delivery.

摘要

阿诺德-奇阿里I型畸形包括小脑扁桃体延长并向下移位至枕骨大孔以下。脊髓空洞症是一种相关的囊肿,可在脊髓内积聚脑脊液,进而压迫局部神经纤维。患有这两种疾病的孕妇格外令人担忧,因为分娩期间发生的生理变化可能导致脑干疝和/或脊柱受压。我们报告两例病例。第一例是一名脊髓空洞症患者,分娩时入院,周围神经症状加重。实施了硬膜外麻醉,她顺利接受了剖宫产,产后症状得到缓解。第二例是一名患有阿诺德-奇阿里I型畸形和脊髓空洞症的患者,分娩时前来就诊。为该患者实施了硬膜外麻醉,使其宫口开全并在胎头+2时完全消退。她在没有产妇自主用力的情况下成功接受了产钳助产。两名患者产后过程均顺利。尽管这些是具有显著潜在发病率的罕见疾病,但通过仔细选择患者,两种分娩方式均可处理分娩过程。我们提醒,本综述的患者数量不足以说明任何一种分娩方式的安全性和有效性,而是侧重于分娩的替代方案。本报告首次记录了一例患有阿诺德-奇阿里畸形和脊髓空洞症的患者在分娩时成功通过阴道分娩处理的病例。

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