Post Nicholas H, Wisoff Jeffrey H, Thorne Charles H, Weiner Howard L
Division of Pediatric Neurosurgery, Department of Neurosurgery, New York University School of Medicine, New York, New York, USA.
Neurosurgery. 2007 Aug;61(2):E426; discussion E426. doi: 10.1227/01.NEU.0000255523.50203.FC.
Transient paraplegia in the immediate postoperative period after lipomyelomeningocele repair is uncommon and is not discussed in the literature. We present the unique case of a patient who developed transient paraplegia 48 hours after lipomyelomeningocele repair attributable to the acute development of a thoracic syrinx.
At birth, the patient was noted to have a large skin-covered mass in the lumbosacral region. On neurological examination, both iliopsoas and quadriceps exhibited 3/5 motor function, and the plantar flexors and dorsiflexors exhibited 1/5 motor function. Urodynamic studies were normal. Magnetic resonance imaging demonstrated the presence of a lipomyelomeningocele associated with tethering of the spinal cord in the lumbosacral region.
At 5 months of age, the patient underwent repair of the lipomyelomeningocele. After surgery, the patient developed progressive paraplegia along with bowel and bladder dysfunction. Given the concern about a postoperative hematoma resulting in cauda equina syndrome, the patient returned to the operating room for a wound exploration. No compressive lesion such as a hematoma was found at surgery. A postoperative magnetic resonance imaging scan obtained afterward, however, demonstrated the presence of a large thoracic syrinx.
Syrinx formation can occur as early as 48 hours after lipomyelomeningocele repair, leading to progressive lower extremity weakness and bowel and bladder incontinence. In the immediate postoperative period, an acute syrinx can mimic cauda equina syndrome, and a magnetic resonance imaging scan is necessary to distinguish between these two entities. In this patient, the syrinx was transient and resolved without a shunting procedure.
脂肪脊髓脊膜膨出修补术后即刻出现短暂性截瘫并不常见,文献中也未对此进行讨论。我们报告了一例独特的病例,该患者在脂肪脊髓脊膜膨出修补术后48小时出现短暂性截瘫,原因是胸段脊髓空洞症急性形成。
出生时,该患者腰骶部有一个大的皮肤覆盖肿物。神经系统检查显示,双侧髂腰肌和股四头肌肌力为3/5,跖屈肌和背屈肌肌力为1/5。尿动力学检查正常。磁共振成像显示腰骶部存在脂肪脊髓脊膜膨出并伴有脊髓拴系。
患者5个月大时接受了脂肪脊髓脊膜膨出修补术。术后,患者出现进行性截瘫以及肠道和膀胱功能障碍。鉴于担心术后血肿导致马尾综合征,患者返回手术室进行伤口探查。手术中未发现血肿等压迫性病变。然而,术后随后进行的磁共振成像扫描显示存在一个大的胸段脊髓空洞症。
脊髓空洞症可在脂肪脊髓脊膜膨出修补术后48小时内出现,导致进行性下肢无力以及肠道和膀胱失禁。在术后即刻,急性脊髓空洞症可类似马尾综合征,需要进行磁共振成像扫描以区分这两种情况。在该患者中,脊髓空洞症是短暂性的,未经分流手术即自行消退。