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A case of Coexistent Persistent Trigeminal and Hypoglossal Arteries Manifested with Neurovascular Compression Syndrome by Hypertension Kosuke Asayama 1 , Kentaro Hayashi 2 , Yukie Kanai 1 , Nao Tahara 1 , Yoshie Kato 1 , Satoshi Abe 2 , Shingo Mitaki 1 , Atsushi Nagai 1 1Department of Neurology, Shimane University Faculty of Medicine 2Advanced Stroke Center, Shimane University Hospital Keyword: 遺残性頸動脈脳底動脈吻合 , 遺残性三叉動脈 , PTA , 遺残性舌下動脈 , PHA , 神経血管圧迫症候群 , persistent carotid-basilar anastomosis , persistent trigeminal artery , persistent hypoglossal artery , neurovascular compression syndrome pp.811-816
Published Date 2022/6/1
DOI https://doi.org/10.11477/mf.1416202125
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Abstract

A 70-year-old woman visited our hospital with hypertension, diplopia, and right orbital pain. Neurological examination revealed right ophthalmoplegia. CT angiography and MRI identified a right persistent trigeminal artery (PTA), right persistent hypoglossal artery, and bovine aortic arch. The right internal carotid artery (ICA) was displaced laterally in the cavernous sinus due to the bifurcation of the PTA. Compression of the right oculomotor nerve, right trochlear nerve, and first division of the right trigeminal nerve by the elongated right ICA was noted and considered a potential cause of the ophthalmoplegia and orbital pain. Symptoms improved with normalization of blood pressure. During embryonic development, the right posterior communicating artery and bilateral vertebral arteries were aplastic or hypoplastic, which suggests that these carotid-basilar anastomoses may have remained as supply routes to provide sufficient blood flow to the posterior cerebral circulation. This is an extremely rare case of embryological implications manifested with neurovascular compression syndrome.

(Received 6 January, 2022; Accepted 17 February, 2022; Published 1 June, 2022)


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電子版ISSN 1344-8129 印刷版ISSN 1881-6096 医学書院

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