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Japanese

Ruptured Persistent Primitive Hypoglossal Artery Aneurysm : case report Atsushi SAWAMURA 1 , Hiroyasu KAMIYAMA 1 , Nobuaki KOBAYASHI 1 , Ken-ichi MAKINO 1 , Katsumi TAKIZAWA 1 , Hiroshi YASUDA 1 , Haruo TAKAMURA 1 1Department of Neurosurgery, Asahikawa Red Cross Hospital Keyword: carotid-basilar anastomosis , persistent primitive hypoglossal artery , subarachnoid hemorrhage , aneurysm , transcondylar approach pp.633-638
Published Date 1999/7/10
DOI https://doi.org/10.11477/mf.1436901749
  • Abstract
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Persistent primitive hypoglossal artery is less common than persistent primitive trigeminal artery. Aboutone hundred examples of such hypoglossal arteries have been demonstrated by angiography. The origin ofpersistent primitive hypoglossal artery is the cervical segment of the internal carotid artery, usually at thelevel of the first to second cervical vertebrae. The artery then enters, with varying degrees of tortuosity,the anterior condyloid (hypoglossal) canal and joins the basilar artery immediately above its lower end. When enlargement of this canal is identified, the presence of a persistent primitive hypoglossal arteryshould be strongly suspected. The homolateral vertebral artery is frequently hypoplasia.

A 66-year-old man was brought to our hospital due to faintness. CT showed thick subarachnoid hemor-rhage. Angiography showed that a persistent primitive hypoglossal artery aneurysm was present, but theposterior communicating artery was absent. Right vertebral angiography showed extravasation clue to re-rupture of the aneurysm. An operation was performed at clay 0 using the left transcondylar approach de-spite deterioration of SAH grading. Intraoperative re-rupturing occurred and the lower cranial nerves clus-tered around the aneurysm, so the aneurysm was partially clipped on the dome. The second angiographywas carried out at clay 10, and there was no vasospasm. Palsy of the lower cranial nerves appeared tran-siently. A ventricle-peritoneum shunt was required due to normal pressure hydrocephalus, but the patientwas discharged with no neurological deficits.


Copyright © 1999, Igaku-Shoin Ltd. All rights reserved.

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電子版ISSN 1882-1251 印刷版ISSN 0301-2603 医学書院

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