Spontaneous Arteriovenous Malformation of the Ear

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Spontaneous Partial Regression of Cerebral Arteriovenous Malformation

Arteriovenous malformation (AVM) of the brain is one of the important pathologic conditions which cause intracerebral or subarachnoid hemorrhage, epilepsy, or chronic cerebral ischemia. The spontaneous regression of cerebral AVM is reported to be very rare and more likely to occur when the AVM is small, is accompanied by hemorrhage, and has fewer arterial feeders. We report a case of right occi...

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Spontaneous resolution of arteriovenous malformation without hemorrhage.

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Spontaneous thrombosis of an arteriovenous malformation.

A patient with a spontaneously thrombosed arteriovenous malformation (AVM) presented with epilepsy. The CT and MRI appearances were of an intrinsic cerebral neoplasm with extensive surrounding vasogenic cerebral oedema and a mass effect. Histopathology confirmed a large thrombosed AVM. The natural history of AVMs and spontaneous thrombosis are reviewed.

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Spontaneous disappearance of a cerebral arteriovenous malformation.

A 63-year-old male presented with a cerebral arteriovenous malformation in the dominant motor area which subsequently disappeared spontaneously. He had suffered from epileptic attacks in his right extremities for 2 years before he first presented aged 53 years. He was treated with anticonvulsants and was followed up. Bleeding from the cerebral arteriovenous malformation occurred when he was 61 ...

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Spontaneous complete regression of cerebral arteriovenous malformation.

A 55 year-old man started with headaches in 2005. He underwent MRI that showed left frontal arteriovenous malformations (AVM) without evidence of hemorrhage. An arteriography revealed AVM supplied by the left anterior cerebral artery (Figures 1A and 1B). In 2010 the patient had an episode of cerebral hemorrhage confirmed with CT and MRI (Figures 2A, 2B and 2C). Referred to our service for treat...

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ژورنال

عنوان ژورنال: Indian Journal of Otolaryngology and Head & Neck Surgery

سال: 2011

ISSN: 2231-3796,0973-7707

DOI: 10.1007/s12070-011-0175-0