This article has Open Peer Review reports available.
Angiographic findings and clinical implications of persistent primitive hypoglossal artery
© Vlychou et al; licensee BioMed Central Ltd. 2003
Received: 27 January 2003
Accepted: 23 July 2003
Published: 23 July 2003
The primitive hypoglossal artery (PHA) is a rare vascular anomaly, which belongs to the group of carotid-basilar anastomosis that may occur in adults.
Herein is presented a case of a patient with a PHA, who had undergone a cerebral angiography due to investigation of subarachnoid hemorrhage. Additionally, the diagnostic alternatives for detection and assessment of PHA and the spectrum of diseases related to its presence are discussed.
The presence of a persistent PHA can be recognized as an incidental finding in a cerebral angiography without any other clinical implication or may be associated with certain clinical entities such as aneurysm formation and atherosclerotic disease.
The primitive hypoglossal artery (PHA) belongs to the group of segmental arteries, which establish the dorsoventral anastomosis during the early fetal life. In the embryo, this dorsoventral anastomosis exists between an anterior arterial system, corresponding to the ventral aorta and a posterior one, located anteriorly in the midline of the neural tube . Segmental arteries at the level of the brainstem are named after the cranial nerves with which they course, and include the trigeminal, otic and hypoglossal artery. Their involution coincides with the development of the posterior communicating artery, which takes place from the 30th to the 40th day of the fetal life. Although these segmental arteries obliterate normally after the 40th day, sporadically such an artery remains patent resulting in a carotid-basilar anastomosis during the adult life, as in the case herein presented. A persistent PHA is related with alterations to the anatomy of cerebral circulation and, although it can be observed as an incidental finding in cerebral angiography, its presence has been associated with clinical implications .
The PHA represents a rare carotid-basilar anastomosis, with a reported incidence between 0.03 and 0.26% on cerebral angiography [2, 3]. The PHA is the second most frequent after the persistent trigeminal artery, which makes up the vast majority of persistent primitive connections, whereas the persistent otic and proatlantal intersegmental arteries (type 1, corresponding to the first segmental artery and type 2, corresponding to the second segmental artery) are less frequent. The characteristics which constitute the criteria for identification of the PHA are described as follows: a) the PHA arises from the cervical part of the internal carotid artery at the C1-C2 level, b) together with the XIIth cranial nerve enters the posterior cranial fossa via the hypoglossal canal, c) the basilar trunk arises from the branch of PHA and d) the ipsilateral vertebral artery may be hypoplastic .
Although conventional angiography has been considered as the reference standard for the detection and evaluation of vascular structures, there are diagnostic alternatives with different advantages. CT angiography is a noninvasive examination, which has the advantage of multiplanar demonstration of the PHA by the use of 3D reconstraction techniques. Therefore, CT angiography provides excellent anatomic localization of PHA in all its parts and depicts clearly its entrance to the hypoglossal canal .
MR imaging and MR angiography in particular is able to sufficiently demonstrate the PHA, withour any contrast medium. MR angiography, by using a maximum-intensity-projection (MIP) program is able to show the complete carotid-basilar anastomosis without superimposition of other vessels [3–5]. Both CT and MR angiography are diagnostic alternatives, which have already been reported in the literature in cases of PHA detection and evaluation of certain pathologic conditions. Thus, stenosis due to atherosclerotic plaque or aneurysm formation can be depicted by 3D CT or MR angiography [6, 7].
Since the presence of PHA may be completely asymptomatic, it may appear as an incidental finding in a cerebral angiogram performed for another diagnostic purpose. However, its identification is clinically important before carotid endarterctomy or skull base surgery . This is obviously related with the fact that both the anterior and posterior cerebral circulation is dependent on the arterial supply of internal carotid artery. The existance of PHA has also been related with increased incidence of aneurysms, arteriovenous malformations and atheroslerotic disease [5–7, 9, 10]. The later may present as a plaque extending from the distal carotid artery into the internal carotid artery (ICA) or as an isolated stenosis near the PHA takeoff. The group of persistent primitive arteries, in which PHA belongs to, is implicated in cases of moyamoya and quasi-moyamoya disease as well [11, 12].
The recognition of PHA as a member of the group of carotid-basilar connections and the reported incidence of related diseases has led to some pathogenetic considerations. There is a hypothesis related to the formation of atherosclerotic plaques affecting the PHA lumen. Because the origin of the PHA from the ICA forms analogous flow dynamics as at the carotid bulb, the development of an atherosclerotic plaque can be expected . Another implication is that in cases of atherosclerotic disease, the clinical assessment of a patient with a PHA may lead to some confusion, due to atypical distribution of cerebral emboli. In addition to that, it has already been suggested that the PHA may be associated with anomalous structure of the vessel wall and exposes the basilar trunk to unusual haemodynamic stress, predisposing to the onset of aneurysms . However, since the above theories have not been yet established, it would be interesting to be investigated in the setting of a multi-center study.
The detection and investigation of an uncommon vascular anomaly, such as the PHA, by an interventional or a non-interventional approach, is of clinical importance, since its presence has been related with a spectrum of diseases. In addition to that, CT and MR angiography due to their 3D capabilities have considerably facilitated the demonstration of the PHA as an anatomic variation.
- Lasjaunias P, Doyon D: The ascending pharyngeal artery and the blood supply of the lower cranial nerves. J Neuroradiol. 1978, 5: 287-301.PubMedGoogle Scholar
- De Caro R, Parenti A, Munari PF: The persistent primitive hypoglossal artery: a rare anatomic variation with frequent clinical implications. Anat Anz. 1995, 177: 193-198.View ArticleGoogle Scholar
- Chaljub G, Guinto FCJ, Crow WN: Persistent Hypoglossal Artery: MRI and MRA findings. J Comp Ass Tomog. 1995, 19: 668-671.View ArticleGoogle Scholar
- Oelerich M, Schuierer G: Primitive hypoglossal artery: demonstration with digital subtaction-, MR- and CT angiography. Eur Radiol. 1997, 7: 1492-1494. 10.1007/s003300050322.View ArticlePubMedGoogle Scholar
- Hahnel S, Hartmann M, Jansen O, Sartor K: Persistent hypoglossal artery: MRI, MRA and digital subtraction angiography. Neuroradiol. 2001, 43: 767-769. 10.1007/s002340100566.View ArticleGoogle Scholar
- Kanai H, Nagai H, Wakabayashi S, Hashimoto N: A large aneurysm of the persistent primitive hypoglossal artery. Neurosurg. 1992, 30: 794-797.View ArticleGoogle Scholar
- Wagner AL: Isolated stenosis of a persistent hypoglossal artery visualized at 3D CT angiography. Am J Neurorad. 2001, 22: 1613-1614.Google Scholar
- Fantini GA, Reilly LM, Stoney RJ: Persistent hypoglossal artery: Diagnostic and therapeutic considerations concerning carotid thromboendarterectomy. J Vasc Surg. 1994, 20: 995-999.View ArticlePubMedGoogle Scholar
- Shibata Y, Hyodo A, Saito A, Yoshii Y, Nose T: Large arteriovenous malformation associated with persistent primitive hypoglossal artery-case report. Neurol Med Chir. 1991, 31: 804-808.View ArticleGoogle Scholar
- Katoh M, Kamiyama H, Kobayashi N, Makino K, Takano K, Tokumitsu N, Takamura H: Severe stenosis of internal carotid artery presenting as loss of consciousness due to presence of primitive hypoglossal artery; case report. Surg Neurol. 1999, 51: 310-312. 10.1016/S0090-3019(98)00053-6.View ArticlePubMedGoogle Scholar
- Komiyama M, Nakajima H, Yasui T, Kitano S, Sakamoto H, Fu Y: High incidence of persistent primitive arteries in moyamoya and quasi-moyamoya disease. Neurol Med Chir. 1999, 39: 416-420.View ArticleGoogle Scholar
- Katayama W, Eromoto T, Yanaki K, Nose T.: Moyamaya disease associated woth persistent primiteve hypoglossal artery: a case report. Ped Neurosurg. 2001, 35: 262-265. 10.1159/000050433.View ArticleGoogle Scholar
- The pre-publication history for this paper can be accessed here:http://www.biomedcentral.com/1471-2342/3/2/prepub
This article is published under license to BioMed Central Ltd. This is an Open Access article: verbatim copying and redistribution of this article are permitted in all media for any purpose, provided this notice is preserved along with the article's original URL.