ruso
вице-маршал авиации catalán
vicemariscal de l'aire 1
Case description: This 53-year-old male with a ruptured left temporal-occipital arteriovenous malformation.
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A case of symptomatic congenital arteriovenous malformation detected in an adult patient is presented.
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Magnetic resonance angiography of the pulmonary artery showed large arteriovenous malformation in the lung.
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A 32-year-old man with a giant abdominoscrotal arteriovenous malformation presented with recurrent heavy bleeding.
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The differential diagnoses considered included a spinal tumour and arteriovenous malformation of the spinal cord.
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In other cases they are due to aneurysm of the ophthalmic artery, to thrombosis of the cavernous sinus, and, in rare instances, to cirsoid aneurysm.
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We report an autopsied 33 year old pregnant woman with racemose hemangioma of the bronchial arteries.
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She was first given a diagnosis of racemose hemangioma of the bronchial arteries at age 19 and underwent surgical ligation.
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Background: Endovascular embolization is being increasingly used to treat cerebral arteriovenous malformations.
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Background: Fistulas and arteriovenous malformations have been occluded using various devices.
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Embolization is a well-established method of treatment of arteriovenous malformations.
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In these 4 cases total ablation of the arteriovenous malformations with alcohol was successful.
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Both CT and MRI showed all arteriovenous malformations and tumors.
Metadata standard for digital astronomical images.
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In both cases the patient was treated with GKS for an AVM.
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Patients: Forty-four randomly selected patients with AVM from the Columbia-Presbyterian AVM Database.
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Objective: To evaluate the vascular architecture of AVM of jaws on DSA.
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Obliteration rates of AVMs and the associated complications after GKS were evaluated.
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Thin-slice MRI acquired for treatment planning did not show the AVM nidus.
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The combination of retinal and intracranial AVMs is known as Wyburn-Mason syndrome.
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The AVM was successfully managed with combined intraarterial embolization and surgical resection.
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Follow-up angiography showed the complete removal of permeable AVM in all patients.
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However, medium AVMs appear to still be at risk for adverse radiation effects.
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The results achieved with excision of these difficult AVM's were good.
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Visual loss is usually the result of optic neuropathy from associated orbitocranial AVMs.
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The natural course of the intracranial AVMs of this syndrome is poorly documented.
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The AVM was completely obliterated 10 months following completion of the radiosurgery treatment.
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Waters' position view and panoramic radiography were indicated for AVMs of the maxilla.
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Eighteen cases of sporadic AVM with operative specimens were included in this study.
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Recently there have been significant developments in the management of AVMs.