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一名患有发育性静脉异常儿童的自发性孤立性非出血性血栓形成：病例报告及文献综述

Spontaneous isolated non-haemorrhagic thrombosis in a child with development venous anomaly: case report and review of the literature.

作者信息

Vieira Santos A, Saraiva P

机构信息

Neuroradiology Department, Garcia de Orta Hospital, Almada, Portugal.

出版信息

Childs Nerv Syst. 2006 Dec;22(12):1631-3. doi: 10.1007/s00381-006-0159-7. Epub 2006 Oct 28.

DOI:10.1007/s00381-006-0159-7
PMID:17072663
Abstract

INTRODUCTION

The natural history of developmental venous anomalies (DVAs) is said to be relatively benign.

CASE REPORT

We herein report the clinical case of a 9-year-old female child with sudden right hemiparesis. An ischaemic infarct secondary to an isolated spontaneous thrombosis of a DVA was diagnosed by brain magnetic resonance imaging, further confirmed by digital subtraction angiography.

CONCLUSION

Considering the therapeutic options, early diagnosis is mandatory.

摘要

引言

发育性静脉异常（DVA）的自然病程据说是相对良性的。

病例报告

我们在此报告一名9岁女童突发右侧偏瘫的临床病例。脑磁共振成像诊断为DVA孤立性自发性血栓形成继发的缺血性梗死，数字减影血管造影进一步证实。

结论

考虑到治疗选择，早期诊断是必需的。

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J Neurosurg. 2004 Oct;101(4):690-3. doi: 10.3171/jns.2004.101.4.0690.
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Intraventricular hemorrhage in a full-term neonate associated with sinus venous thrombosis and homozygosity for the plasminogen activator inhibitor-1 4G/4G polymorphism.一名足月儿发生脑室内出血，与静脉窦血栓形成及纤溶酶原激活物抑制剂-1 4G/4G基因多态性纯合子相关。
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儿童脑发育性静脉异常——影像学表现及进展
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Epilepsy in a boy with a developmental venous anomaly--case-based update.一名患有发育性静脉异常男孩的癫痫——基于病例的最新情况
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