Open Access
CC BY-NC-ND 4.0 · Indian J Radiol Imaging 2020; 30(03): 383-385
DOI: 10.4103/ijri.IJRI_429_19
Case Report

Unusual case of persistent primitive hypoglossal artery with anterior choroidal artery aneurysm in Chiari type I malformation

Shinya Haryu
Department of Neurosurgery, Kanuma Neurosurgical Clinic, Tochigi
Department of Neurosurgery, Tohoku University Graduate School of Medicine, Sendai, Japan
,
Naoki Shida
Department of Neurosurgery, Tohoku University Graduate School of Medicine, Sendai, Japan
,
Teiji Tominaga
Department of Neurosurgery, Kanuma Neurosurgical Clinic, Tochigi
› Author Affiliations

Financial support and sponsorship Nil.
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Abstract

Persistent primitive hypoglossal artery (PPHA) is a rare form of persistent embryonic carotid-basilar anastomosis. We present an unusual case of PPHA and an anterior choroidal artery (AChoA) aneurysm associated with Chiari type I malformation. A 45-year-old woman presented with transient dizziness. Magnetic resonance imaging revealed Chiari type I malformation and a left AChoA aneurysm. Digital subtraction angiography incidentally revealed a left PPHA. To the best of our knowledge, this is the first reported case of Chiari malformation in conjunction with PPHA and aneurysms. In this case, the perfusion of the posterior circulation is completely dependent on PPHA. It is very important to identify such variant vessels and complex angioarchitecture before planning neuroendovascular or surgical intervention to prevent possible risks.



Publication History

Received: 23 October 2019

Accepted: 03 May 2020

Article published online:
19 July 2021

© 2020. Indian Radiological Association. This is an open access article published by Thieme under the terms of the Creative Commons Attribution-NonDerivative-NonCommercial-License, permitting copying and reproduction so long as the original work is given appropriate credit. Contents may not be used for commercial purposes, or adapted, remixed, transformed or built upon. (https://creativecommons.org/licenses/by-nc-nd/4.0/).

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