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本文引用的文献

1
Anatomoclinical Aspects of Dural Arteriovenous Shunts in Children. Review of 29 cases.儿童硬脑膜动静脉分流的解剖临床学方面。29例病例回顾。
Interv Neuroradiol. 1996 Sep 30;2(3):179-91. doi: 10.1177/159101999600200303. Epub 2001 May 15.
2
Dural arteriovenous fistula in children: endovascular treatment and outcomes in seven cases.儿童硬脑膜动静脉瘘：7例血管内治疗及结果
AJNR Am J Neuroradiol. 2001 Jun-Jul;22(6):1217-25.
3
Spontaneous obliteration of pial arteriovenous malformations: a review of 27 cases.软脑膜动静脉畸形的自然闭塞：27例病例回顾
AJNR Am J Neuroradiol. 2001 Mar;22(3):531-6.
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Embolization of a giant torcular dural arteriovenous fistula in a neonate.新生儿巨大窦汇区硬脑膜动静脉瘘的栓塞治疗
Pediatr Neurosurg. 1999 May;30(5):258-62. doi: 10.1159/000028807.
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Severe cerebral venous sinus thrombosis and dural arteriovenous fistula in an infant with protein S deficiency.一名患有蛋白S缺乏症的婴儿出现严重脑静脉窦血栓形成和硬脑膜动静脉瘘。
Childs Nerv Syst. 1999 Mar;15(2-3):128-30. doi: 10.1007/s003810050349.
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Transumbilical embolization of a congenital dural arteriovenous fistula at the torcular herophili in a neonate. Case report.新生儿窦汇区先天性硬脑膜动静脉瘘的经脐栓塞术。病例报告。
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Neurosurgery. 1995 Dec;37(6):1193-9; discussion 1199-200. doi: 10.1227/00006123-199512000-00020.
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Posterior dural arteriovenous malformation and medulloblastoma in an infant: case report.
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Posterior dural arteriovenous malformations in infancy.婴儿期后颅窝硬脑膜动静脉畸形
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婴儿硬脑膜窦瘘伴软膜增生的自然消退

Spontaneous regression of an infantile dural sinus fistula with pial recruitment.

作者信息

Goddard Anthony J P, Phatouros Constatine C, Khangure Makmon S

机构信息

Interventional Neuroradiology Unit, Royal Perth Hospital, Perth, Western Australia 6847.

出版信息

AJNR Am J Neuroradiol. 2002 Oct;23(9):1482-4.

PMID:12372735
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7976782/
Abstract

Infantile dural sinus fistulas are rare and generally have a poor prognosis unless treatment can be undertaken. We report a unique case of an infantile dural sinus fistula with secondary pial recruitment that was managed conservatively. Subsequent spontaneous regression of the lesion occurred over 11 months. The clinical and angiographic features that indicated a probable favorable prognosis are discussed.

摘要

婴儿硬脑膜窦瘘罕见，除非进行治疗，一般预后较差。我们报告一例独特的婴儿硬脑膜窦瘘伴继发性软膜增生，该病例采用保守治疗。随后病变在11个月内自行消退。文中讨论了提示可能预后良好的临床和血管造影特征。