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小儿创伤性后颅窝硬膜外血肿:单中心病例系列

Liquid Posterior Fossa Epidural Hematoma in Pediatric Trauma: A Single-Center Case Series.

作者信息

Han Kun, Li Zhaojian, Yin Hongwei, Yao Weicheng, Lan Xiaolei, Bo Yongli

机构信息

Department of Neurosurgery, Affiliated Hospital of Qingdao University, Qingdao, China.

出版信息

J Neurol Surg A Cent Eur Neurosurg. 2018 Sep;79(5):380-385. doi: 10.1055/s-0038-1648225. Epub 2018 Jun 14.

Abstract

BACKGROUND

Liquid posterior fossa epidural hematoma (LPFEH) following head trauma is uncommon, and very few such cases have been described in the literature. Eight patients with this entity and their treatments are presented here.

METHODS

We performed a single-institution retrospective analysis of all patients with diagnosed LPFEH over a 3-year period. Collected data included clinical history, laboratory results, treatment, and review of all imaging studies performed.

RESULTS

Eight pediatric cases were identified with imaging findings consistent with LPFEH; no adult case was identified. Enlargement of ventricles appeared on computed tomography (CT) in six cases, and secondary epilepsy onset occurred in three cases with severe dilated ventricles. Routine hematologic and coagulation tests failed to disclose anemia or abnormal coagulation in each case. Five patients underwent burr-hole drainage of the hematoma and recovered completely. Conservative therapy was adopted in three patients for small hematomas, and hematoma enlargement was not observed in the follow-up CT scans.

CONCLUSIONS

LPFEH is a rare subtype of traumatic epidural hematoma specifically recognized in the pediatric population. Minimally invasive burr-hole drainage is a feasible procedure for the patient with evident space-occupying effect. Coagulation dysfunction or low hemoglobin as a possible contributing factor and its role in formation of LPFEH was excluded.

摘要

背景

头部外伤后发生的后颅窝硬膜外血肿(LPFEH)并不常见,文献中描述的此类病例很少。本文介绍了8例该病症患者及其治疗情况。

方法

我们对一家机构在3年期间内所有诊断为LPFEH的患者进行了回顾性分析。收集的数据包括临床病史、实验室检查结果、治疗情况以及对所有进行过的影像学检查的复查。

结果

通过影像学检查发现8例儿科病例符合LPFEH表现;未发现成人病例。6例患者的计算机断层扫描(CT)显示脑室扩大,3例脑室严重扩张的患者出现继发性癫痫发作。常规血液学和凝血检查未发现每例患者有贫血或凝血异常。5例患者接受了血肿钻孔引流术并完全康复。3例小血肿患者采用保守治疗,随访CT扫描未发现血肿增大。

结论

LPFEH是创伤性硬膜外血肿的一种罕见亚型,在儿科人群中较为特殊。对于有明显占位效应的患者,微创钻孔引流是一种可行的治疗方法。排除了凝血功能障碍或低血红蛋白作为可能的促成因素及其在LPFEH形成中的作用。

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