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.
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。
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