Spontaneous spinal epidural hematoma in children: a case report and literature review.

Q1 Medicine Journal of spine surgery Pub Date : 2024-09-23 Epub Date: 2024-08-26 DOI:10.21037/jss-24-49
Marthinson Andrew Tombeng, Kazuma Doi, Tjokorda Gde Bagus Mahadewa, Satoshi Tani, Junichi Mizuno
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Abstract

Background: Spontaneous spinal epidural hematoma (SSEH) is a hematoma within the spinal epidural space without the underlying causes of trauma or iatrogenic and is considered a very rare neurosurgical emergency disease in children that can cause spinal cord compression and neurological dysfunction. This article provides useful information and guidance to the clinician about SSEH in children regarding its specific characteristics, clinical presentation, and management strategy to achieve a better outcome.

Case description: A 14-year-old boy presented with an acute onset of neck pain radiating to the right shoulder and progressive right hemiparesis. The cervical spine magnetic resonance imaging (MRI) revealed a right posterolateral hyperacute spinal epidural hematoma at C4-C7. The patient underwent an emergent open-door laminoplasty (C5-C6) with partial laminectomy (C4 and C7) and complete evacuation of the hematoma. The patient had a complete recovery after surgery with no neurological deficits. A literature search in the PubMed electronic database was performed to identify published English articles between January 2000 to December 2023 focusing on SSEH in children. We have found 81 articles with a total of 95 cases of SSEH in children, providing comparison data on sex, age, clinical presentation, etiology, location of the hematoma, treatment modalities, and outcomes.

Conclusions: SSEH in children is a very rare neurosurgical emergency disease. Prompt and proper examination is essential to establish the diagnosis and early surgical decompression. Adequate surgical decompression may reduce intradural pressure and increase the blood perfusion to the spinal cord, thus, this will eventually reduce ischemia and prevent secondary spinal injury. As a result, complete recovery can be expected.

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儿童自发性脊柱硬膜外血肿:病例报告和文献综述。
背景:自发性脊髓硬膜外血肿(SSEH)是脊髓硬膜外腔内的血肿,其根本原因不是外伤或先天性的,被认为是一种非常罕见的儿童神经外科急诊疾病,可导致脊髓压迫和神经功能障碍。本文就儿童 SSEH 的具体特征、临床表现和处理策略为临床医生提供有用的信息和指导,以获得更好的治疗效果:一名 14 岁男孩因颈部疼痛急性发作并向右肩放射,同时伴有进行性右侧偏瘫。颈椎磁共振成像(MRI)显示,C4-C7 处存在右侧后外侧急性脊髓硬膜外血肿。患者接受了紧急开门椎板成形术(C5-C6)和部分椎板切除术(C4 和 C7),并完全清除了血肿。术后患者完全康复,无神经功能障碍。我们在 PubMed 电子数据库中进行了文献检索,以找出 2000 年 1 月至 2023 年 12 月期间发表的以儿童 SSEH 为主题的英文文章。我们找到了81篇文章,共95例儿童SSEH病例,提供了性别、年龄、临床表现、病因、血肿位置、治疗方式和结果等方面的对比数据:儿童 SSEH 是一种非常罕见的神经外科急诊疾病。及时、正确的检查对确诊和早期手术减压至关重要。适当的手术减压可降低硬膜内压,增加脊髓的血液灌注,从而最终减少缺血,防止继发性脊髓损伤。因此,患者有望完全康复。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Journal of spine surgery
Journal of spine surgery Medicine-Surgery
CiteScore
5.60
自引率
0.00%
发文量
24
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