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硬脑膜动静脉畸形中的额部间歇性节律性δ活动(FIRDA)

Frontal intermittent rhythmic delta activity (FIRDA) in pial-dural arteriovenous malformation.

作者信息

Nazarian S M, Potts R E, Chesser M Z, Janati A

机构信息

Neurology Service, John L. McClellan Memorial Veterans Hospital, Little Rock, Arkansas 72205.

出版信息

Clin Electroencephalogr. 1987 Oct;18(4):227-32.

PMID:3665110
Abstract

We report a case of FIRDA associated with a pial-dural arteriovenous malformation (AVM). The patient presented with headaches, papilledema and partial oculomotor nerve palsy. CT scan had failed to discover the AVM. After partial embolization of the AVM, the patient's symptoms and signs resolved, and the FIRDA disappeared. FIRDA has been thought to be caused by frontal lobe ischemia or periventricular edema. It has not been reported in benign intracranial hypertension (BIH). We postulate that the FIRDA in this case was due to the circulatory "steal" effect of the AVM, and not to the intracranial hypertension. Five percent of patients with dural AVM's present with a picture consistent with BIH. We recommend a diligent search for additional pathology if FIRDA is seen in association with presumed BIH.

摘要

我们报告一例与软脑膜-硬脑膜动静脉畸形(AVM)相关的额叶间歇性节律性放电(FIRDA)。患者表现为头痛、视乳头水肿和部分动眼神经麻痹。CT扫描未能发现AVM。AVM部分栓塞后,患者的症状和体征消失,FIRDA也消失了。FIRDA一直被认为是由额叶缺血或脑室周围水肿引起的。在良性颅内高压(BIH)中尚未有相关报道。我们推测该病例中的FIRDA是由于AVM的循环“盗血”效应,而非颅内高压所致。5%的硬脑膜AVM患者表现出与BIH一致的症状。如果在疑似BIH的病例中发现FIRDA,我们建议仔细寻找其他病变。

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