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儿童自发性脊髓硬膜外血肿的治疗:25 例分析。

Treatment of spontaneous spinal epidural hematoma in children: analysis of 25 cases.

机构信息

Di Rocco Center of Pediatric Neurosurgery, Department of Neurosurgery, Xuanwu Hospital, Capital Medical University, Beijing, China.

出版信息

Childs Nerv Syst. 2022 Aug;38(8):1557-1566. doi: 10.1007/s00381-022-05459-x. Epub 2022 May 30.

Abstract

INTRODUCTION

Spontaneous spinal epidural hematoma (SSEH) is a rare neurosurgical emergency, presenting as sudden onset of back pain and weakness of lower extremities. Many patients have no definite cause. Some cases of SSEH caused by vascular malformation have been reported. The treatment strategy remains controversial. This study aimed to analyze the causes of SSEH and proposed a treatment strategy according to clinical outcomes of patients at a single institution.

METHODS

A total of 25 cases of SSEH under 18 years of age treated between March 2004 and July 2021 were retrospectively analyzed.

RESULTS

The mean age of the first SSEH onset was 7.1 years. The most common location was cervicothorax. Nine patients suffered from multiple episodes. Twenty-three patients underwent spinal digital subtraction angiography (DSA), of which seven (30.4%) patients had positive findings: three cases had epidural artery venous fistula (AVF), two cases had epidural artery venous malformation (AVM), and two cases had abnormal concentration of contrast agent. Seventeen patients received surgery. Eleven patients (44%) were diagnosed as vascular malformation by either DSA or pathology. The follow-up rate was 80%, with 20 patients (80%) achieving satisfactory clinical outcome. Risk factors for poor clinical outcome included multiple episodes (p = 0.028) and higher Aminoff-Logue score (p = 0.005).

CONCLUSION

Spinal epidural vascular malformation is a significant cause of SSEH. Spinal DSA is necessary. Surgery should be recommended for patients with multiple episodes, positive findings on DSA, or severe neurological deficits. Conservation therapy can be considered for other patients, but long-time follow-up is necessary.

摘要

简介

自发性硬脊膜外血肿(SSEH)是一种罕见的神经外科急症,表现为突发背痛和下肢无力。许多患者没有明确的病因。已有报道称一些 SSEH 是由血管畸形引起的。治疗策略仍存在争议。本研究旨在分析 SSEH 的病因,并根据单一机构患者的临床结果提出治疗策略。

方法

回顾性分析 2004 年 3 月至 2021 年 7 月期间收治的 25 例年龄在 18 岁以下的 SSEH 患者。

结果

首次 SSEH 发作的平均年龄为 7.1 岁。最常见的部位是颈胸段。9 例患者反复发作。23 例行脊柱数字减影血管造影(DSA)检查,其中 7 例(30.4%)阳性发现:3 例硬膜外动静脉瘘(AVF),2 例硬膜外动静脉畸形(AVM),2 例造影剂浓度异常。17 例行手术治疗。11 例(44%)患者通过 DSA 或病理诊断为血管畸形。随访率为 80%,20 例(80%)患者的临床结局满意。预后不良的危险因素包括反复发作(p=0.028)和较高的 Aminoff-Logue 评分(p=0.005)。

结论

脊柱硬膜外血管畸形是 SSEH 的重要病因。脊髓 DSA 是必要的。对于反复发作、DSA 阳性发现或严重神经功能缺损的患者,应推荐手术治疗。对于其他患者,可以考虑保守治疗,但需要长期随访。

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