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首页> 外文期刊>European journal of paediatric neurology: EJPN : official journal of the European Paediatric Neurology Society >Spontaneous spinal epidural hematoma in infancy: Review of the literature and the 'seventh' case report
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Spontaneous spinal epidural hematoma in infancy: Review of the literature and the 'seventh' case report

机译:婴儿期自发性脊髓硬膜外血肿:文献复习和“第七例”病例报告

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摘要

Spontaneous spinal epidural hematomas (SSEH) are a rare cause of spinal cord compression in childhood and especially in infancy. We reviewed the literature and describe a case of an 8-month-old boy with a large spontaneous cervico-thoracic epidural hematoma. With this review we want to detail the importance of early investigation, diagnosis and treatment in infants with SSEH. In our case the infant presented with irritability and crying and an ascending paralysis within four days. Magnetic resonance imaging (MRI) of the spine demonstrated an extensive epidural hematoma between C5 and L1, serious medullar compression and secondary cervical and thoracic medullar edema and hydromyelia. An emergency laminectomy was performed with evacuation of a well organized hematoma. There was a partial recuperation of the neurologic symptoms. Based on the scarce literature which only concerns seven case reports, SSEH is a rare cause of spinal compression in infancy. The presentation is often not specific and neurological symptoms are often lacking in the beginning. However early diagnosis with MRI and prompt neurosurgical intervention are importnt to improve outcome.
机译:自发性脊髓硬膜外血肿(SSEH)是儿童(尤其是婴儿期)脊髓受压的罕见原因。我们回顾了文献并描述了一个8个月大的男孩,该男孩患有大型自发性颈胸硬膜外血肿。通过这篇综述,我们想详细说明SSEH婴儿早期调查,诊断和治疗的重要性。在我们的病例中,婴儿在四天内表现出烦躁,哭闹和麻痹性上升。脊柱的磁共振成像(MRI)显示C5和L1之间广泛的硬膜外血肿,严重的髓样压迫以及继发的颈髓和胸髓样水肿和髓鞘积水。进行紧急椎板切除术并排空组织良好的血肿。神经系统症状有所恢复。基于仅涉及七个病例报告的稀有文献,SSEH是婴儿期脊髓受压的罕见原因。表现通常不具体,一开始常常缺乏神经系统症状。然而,MRI的早期诊断和及时的神经外科干预对于改善预后至关重要。

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