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妊娠中的马尾神经:早期管理与结局

Cauda Equina in Pregnancy: Early Management and Outcome.

作者信息

Yildiz Dara, Irwin Shane C, Ozgokce Gul Helin, Ledingham Conor, Hughes Bridget

机构信息

Trauma and Orthopaedics, Mayo University Hospital, Castlebar, IRL.

出版信息

Cureus. 2025 Apr 14;17(4):e82274. doi: 10.7759/cureus.82274. eCollection 2025 Apr.

Abstract

Cauda equina syndrome (CES) is a rare but serious clinical presentation characterised by compression of the lumbosacral nerve roots below the conus medullaris, resulting in lower back pain, bilateral sciatica, motor and sensory deficits, and bladder or bowel dysfunction. Its occurrence in pregnancy is exceptionally rare and poses significant diagnostic and management challenges. We present the case of a 34-year-old woman at 22 weeks' gestation following in vitro fertilization (IVF) who developed acute bilateral leg pain, lower limb weakness, and urinary retention following a three-day history of backache. Neurological examination revealed reduced lower limb power, saddle anaesthesia, and loss of perianal sensation with absent ankle reflexes. MRI demonstrated a large L5/S1 disc extrusion completely filling the spinal canal. Following multidisciplinary assessment, she underwent urgent surgical decompression via left L5/S1 laminotomy within eight hours of symptom onset. A large sequestrated disc fragment was removed, and the nerve root canal decompressed. Post-operatively, the patient reported immediate relief of radicular pain and gradual return of bladder function and motor strength. Her pregnancy continued without complication, and she delivered a healthy baby by elective caesarean section at 38 weeks. At four-month follow-up, she had made a full recovery with complete resolution of neurological symptoms apart from mild residual back pain. This case highlights the importance of prompt recognition and early intervention in CES during pregnancy. A multidisciplinary approach is essential to facilitate timely imaging and surgery while ensuring maternal and fetal safety.

摘要

马尾综合征(CES)是一种罕见但严重的临床表现,其特征为脊髓圆锥以下的腰骶神经根受压,导致下背部疼痛、双侧坐骨神经痛、运动和感觉功能障碍以及膀胱或肠道功能障碍。其在妊娠期的发生极为罕见,给诊断和治疗带来了重大挑战。我们报告一例34岁体外受精(IVF)后妊娠22周的女性病例,该患者在背痛三天后出现急性双侧腿痛、下肢无力和尿潴留。神经系统检查显示下肢肌力减弱、鞍区感觉缺失、肛周感觉丧失且踝反射消失。磁共振成像(MRI)显示一个巨大的L5/S1椎间盘突出,完全占据了椎管。经过多学科评估,她在症状出现后八小时内通过左侧L5/S1椎板切开术接受了紧急手术减压。移除了一个巨大的游离椎间盘碎片,并对神经根通道进行了减压。术后,患者报告神经根性疼痛立即缓解,膀胱功能和肌力逐渐恢复。她的妊娠继续进行且无并发症,在38周时通过择期剖宫产分娩了一个健康的婴儿。在四个月的随访中,除了轻度残留背痛外,她已完全康复,神经症状完全消失。该病例强调了妊娠期及时识别和早期干预CES的重要性。多学科方法对于促进及时成像和手术,同时确保母婴安全至关重要。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/91ce/12078998/8c1ddd2cec89/cureus-0017-00000082274-i01.jpg

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