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婴儿硬膜下血肿:会自发发生吗?来自前瞻性系列研究的数据及对文献的批判性综述。

Subdural hematoma in infants: can it occur spontaneously? Data from a prospective series and critical review of the literature.

作者信息

Vinchon Matthieu, Delestret Isabelle, DeFoort-Dhellemmes Sabine, Desurmont Marie, Noulé Nathalie

机构信息

Department of Pediatric Neurosurgery, University Hospital, Lille, France.

出版信息

Childs Nerv Syst. 2010 Sep;26(9):1195-205. doi: 10.1007/s00381-010-1105-2. Epub 2010 Feb 27.

Abstract

BACKGROUND

Subdural hematomas (SDH) in infants often result from nonaccidental head injury (NAHI), which is diagnosed based on the absence of history of trauma and the presence of associated lesions. When these are lacking, the possibility of spontaneous SDH in infant (SSDHI) is raised, but this entity is hotly debated; in particular, the lack of positive diagnostic criteria has hampered its recognition. The role of arachnoidomegaly, idiopathic macrocephaly, and dehydration in the pathogenesis of SSDHI is also much discussed.

PURPOSE

We decided to analyze apparent cases of SSDHI from our prospective databank.

MATERIALS AND METHODS

We selected cases of SDH in infants without systemic disease, history of trauma, and suspicion of NAHI. All cases had fundoscopy and were evaluated for possible NAHI. Head growth curves were reconstructed in order to differentiate idiopathic from symptomatic macrocrania.

RESULTS

Sixteen patients, 14 males and two females, were diagnosed with SSDHI. Twelve patients had idiopathic macrocrania, seven of these being previously diagnosed with arachnoidomegaly on imaging. Five had risk factors for dehydration, including two with severe enteritis. Two patients had mild or moderate retinal hemorrhage, considered not indicative of NAHI. Thirteen patients underwent cerebrospinal fluid drainage. The outcome was favorable in almost all cases; one child has sequels, which were attributable to obstetrical difficulties.

CONCLUSION

SSDHI exists but is rare and cannot be diagnosed unless NAHI has been questioned thoroughly. The absence of traumatic features is not sufficient, and positive elements like macrocrania, arachnoidomegaly, or severe dehydration are necessary for the diagnosis of SSDHI.

摘要

背景

婴儿硬膜下血肿(SDH)常由非意外性头部损伤(NAHI)引起,其诊断基于无外伤史及相关损伤的存在。当缺乏这些时,婴儿自发性SDH(SSDHI)的可能性增加,但这一实体存在激烈争论;特别是缺乏阳性诊断标准阻碍了其识别。蛛网膜肥大、特发性巨头畸形和脱水在SSDHI发病机制中的作用也备受讨论。

目的

我们决定分析来自前瞻性数据库中明显的SSDHI病例。

材料与方法

我们选择了无全身性疾病、外伤史且无NAHI怀疑的婴儿SDH病例。所有病例均进行了眼底检查,并评估是否可能为NAHI。重建头部生长曲线以区分特发性与症状性巨头症。

结果

16例患者被诊断为SSDHI,其中14例男性,2例女性。12例患者有特发性巨头症,其中7例之前影像学诊断为蛛网膜肥大。5例有脱水危险因素,包括2例重症肠炎患者。2例患者有轻度或中度视网膜出血,认为不提示NAHI。13例患者接受了脑脊液引流。几乎所有病例预后良好;1名儿童有后遗症,归因于产科困难。

结论

SSDHI确实存在,但很罕见,除非对NAHI进行了彻底排查,否则无法诊断。缺乏外伤特征并不足够,巨头症、蛛网膜肥大或严重脱水等阳性因素对于SSDHI的诊断是必要的。

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