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DISSECTING ANEURYSM OF THE VERTEBRO-BASIRAL ARTERY : A CASE REPORT AND REVIEW OF PREVIOUS CASES Kyohji Takita 1 , Hideo Shirato 1 , Toshiko Akasaka 1 , Hitoshi Hukazawa 2 1Department of Neurology, Nakadohri Hospital 2Department of Pathology, Akita Research Institute of Brain and Blood Vessels pp.1211-1218
Published Date 1979/12/1
DOI https://doi.org/10.11477/mf.1406204505
  • Abstract
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A intracranial dissecting aneurysm is exceedingly rare condition as compared as dissecting aneurysm of the aorta. A case of dissecting aneurysm of the vertebro-basiral artery with episodes of TIA, terminally subarachnoid hemorrhage was reported.

A 33-year-old man was admitted to Nakadohri Hospital on Oct. 12, 1975, with complaints of headache, vomiting and weakness of the left upper and lower extremities. He had a history of essential hypertension and episodes of transient attack of blurred vision, headache and vomiting before four months.

On examination, he was drawsy and slightly confused. Blood pressure was 223/130 mmHg, pulse rate 81. Neurologically, he had a minimal left hemiparesis with bilateral Babinski sign and his eyes were deviated to the right. The spinal tap revealed clear, colorless CSF with an open pressure of 120 mm of water. The right carotid angiography performed soon after admission showed slight narrowing of the trunk of middle cerebral artery.

The hemiparesis was gradually improving but on Oct. 14, he suddenly complained of severe headache and then he was comatose. The spinal tap soon after the attack revealed bloody CSF. An emergency selective left vertebral angiogram disclosed fusiform-aneurysms of terminal portions of the bilateral vertebral arteries and occlusion of the left posterior cerebral artery. He died 4 days after the last attack.

Autopsied brain revealed marked subarachnoid hemorrhage in the base of the pons and frontal base. The vertebral arteries were dilated at the prejunctional portions.

The coronal section of the brain disclosed edematous swelling and hemorrhagic infarction in the territory of the left posterior cerebral artery.

Microscopically, the basiral artery was dissected between media and adventitia and the true lumen was compressed by hematoma in dissecting false lumen. There were marked thrombotic stenoses of the trunks of anterior, middle, and posterior cerebral arteries. The cause of the dissecting aneurysm of this case was not obscure but arterio-sclerosis and congenital defect of internal lamina was suspected.

The disease in the literature, presented an acute onset of stroke and stenotic or complete occlusive lesions were demonstrated on angiogram. The true subarachnoid hemorrhage of intracranial dissecting aneurysm was rare condition such as our case.


Copyright © 1979, Igaku-Shoin Ltd. All rights reserved.

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電子版ISSN 2185-405X 印刷版ISSN 0006-8969 医学書院

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