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Artery of Percheron as a Rare Feeder of Hemorrhagic Thalamic Arteriovenous Malformation: A Case Report and Literature Review

Authors Zhang M, Feng Z, Yu W, Fu C

Received 28 August 2020

Accepted for publication 24 September 2020

Published 6 October 2020 Volume 2020:13 Pages 771—774

DOI https://doi.org/10.2147/IJGM.S279226

Checked for plagiarism Yes

Review by Single anonymous peer review

Peer reviewer comments 2

Editor who approved publication: Dr Scott Fraser

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Mengchao Zhang1 *,* Zheng Feng2 *,* Weidong Yu,3 Chao Fu3

1Department of Radiology, China-Japan Union Hospital of Jilin University, Changchun, Mainland China; 2Department of Pediatrics, China-Japan Union Hospital of Jilin University, Changchun, Mainland China; 3Department of Neurosurgery, China-Japan Union Hospital of Jilin University, Changchun, Mainland China

*These authors contributed equally to this work

Correspondence: Chao Fu Email [email protected]

Abstract: Arteriovenous malformation (AVM) fed by the artery of Percheron (AOP) is extremely rare, with only one case described in the literature to date. We herein present a case of a 43-year-old female with hemorrhagic thalamic AVM mainly supplied by the AOP, who subsequently underwent conservative management and recovered well except for mild right hemiparesis. This case highlights that the AOP is a rarely recognized but clinically significant entity and should be identified when dealing with AOP-associated neurovascular disorder as described.

Keywords: artery of Percheron, anatomic variant, thalamic hemorrhage, arteriovenous malformation

Introduction

According to the Percheron’s classification, there are four anatomic variants of blood supply to the midbrain and thalami.1 In type I, the most common variant, paired thalamic and midbrain perforating arteries arise from the bilateral P1 segments of the posterior cerebral artery (PCA) individually. In type II, multiple perforating vessels (type IIa) or a single unpaired trunk (the artery of Percheron, AOP) originates from the unilateral P1 segment (type IIb) supplying the bilateral paramedian thalami and rostral midbrain. In type III, an arterial arcade bridges the bilateral P1 segments giving out multiple small branches to the midbrain and thalami.

To date, the most frequent event regarding the AOP is symmetric bilateral thalamic infarcts, accounting for approximately 0.1–2% of all ischemic strokes.25 The symptomatology of the AOP stroke includes altered mental status, oculomotor abnormality, memory impairment, behavioral amnesic impairment, aphasia or dysarthria, hemiplegia, and cerebellar signs.27 It is worthy of note that the AOP is rarely seen in most of the reported cases because it is too small to be visualized on routine brain imaging.

Notably, the AOP as a feeding artery of an arteriovenous malformation (AVM) is exceedingly rare, and only one case, to our best knowledge, has been reported.6 We herein present a case of a 43-year-old woman with hemorrhagic thalamic AVM mainly fed by the AOP, and the potential clinical importance of this variant, as well as the treatment strategy of the AOP-associated AVM, is discussed.

Case Presentation

A previously healthy 43-year-old female was initially admitted to another hospital with a sudden onset of severe headache, nausea and right hemiparesis (1/5). Non-contrast brain computed tomography (CT) revealed a left thalamic hemorrhage with an adjacent calcified lesion and intraventricular hemorrhage (Figure 1A). No evidence of acute hydrocephalus was observed. Conservative therapy was instituted, and she was discharged 20 days later with mild right hemiparesis (4/5). Subsequently, the patient was referred for further evaluation. Head CT revealed the disappearance of the hematoma (Figure 1B). Catheter-based angiography showed an AVM fed by a tortuous AOP arising from the left PCA and draining upward through the left internal cerebral vein into the vein of Galen (Figure 2). The P1 segment of the ipsilateral PCA was not absent or hypoplastic.

Figure 1 Brian computed tomography (CT) image (A) showing a left thalamic hemorrhage (asterisk) adjacent to a calcified lesion (arrowhead), extending into the ventricular system. Head CT image on day 20 (B) showing that the hematoma was spontaneously resolved and the adjacent calcifications (arrowhead) existed.

Figure 2 Catheter-based angiograms (A-D) revealing an artery of Percheron (arrow) arising from the left posterior cerebral artery (PCA), running upward, then taking a marked tortuous course, and feeding an arteriovenous malformation (AVM, arrowhead) in the left thalamus. The AVM drained into the vein of Galen through the left internal cerebral vein. Please note that the ipsilateral P1 segment of the PCA was not absent or hypoplastic.

Endovascular embolization of the AVM via the AOP as the first choice was recommended; moreover, microsurgical resection or stereotactic radiosurgery was provided an alternative option. However, she declined to undergo intervention given that the risks, and thereafter, was treated conservatively. Her neurological condition remained stable during a 1-year follow-up.

Discussion

To date, the prevalence of AOP is unclear because of its rarity. AOP often poses a diagnostic challenge because it is too small to be seen by routine brain imaging. It is noteworthy that the V sign on axial fluid-attenuated inversion recovery and/or diffusion-weighted imaging, a V-shaped hyperintensity along the pial surface of the midbrain in the interpeduncular fossa, was identified in 38% of all cases and 67% of cases with AOP infarction, respectively.5 Moreover, AOP has been found during a neuroendoscopic surgery for suprasellar arachnoid cyst.7

AOP may be of clinical importance in particular circumstances, such as diagnostic or therapeutic procedure because the injury of this artery during neuroendoscopic surgery and cerebral angiography has been reported to result in acute bilateral thalamic infarcts.8,9

Notably, AOP is rare but potentially involved in hemorrhagic AVM. As far as we know, only one case has been previously presented in the literature (Table 1).6 Moreover, the treatment challenge can exist when dealing with AOP-associated AVM. Motegi et al failed to embolize a thalamic AVM fed by AOP due to the inaccessibility of the thalamoperforating artery via the tortuous AOP.6 In this study, endovascular embolization of the AVM nidus via the AOP seemed to be feasible. As such, we recommended endovascular embolization of the AVM as the first choice. However, it should be mentioned that AOP injury or thrombosis may carry a risk of bilateral thalamic infarcts. Moreover, the AVM can also be amenable to resection if a surgical corridor is available through the hematoma, as described in a previous study.6 In addition, stereotactic radiosurgery has become increasingly recommended for the AVMs less than 3 cm in diameter and located in deep or eloquent areas of the brain, with a reported cure rate of 81%-90%.10 Although this method avoids a craniotomy, its main risks are twofold. First, the radiation can induce injury to the adjacent brain tissues; second, a latency period of approximately 1–3 years exists before potentially complete obliteration, in which a risk of bleeding remains.10,11 Our patient thought that the risks of the above-mentioned treatment options outweighed the benefits, and chose conservative treatment.

Table 1 Reported Cases with AVM Fed by the AOP

Conclusion

AOP is a rarely recognized but clinically significant anatomic variant, and thus identifying this vessel is of importance when treating AOP-associated neurovascular disorder as described in this study.

Data Sharing Statement

The authors declare that they had full access to all of the data in this study, and the authors take complete responsibility for the integrity of the data. All original data are available in the China-Japan Union Hospital of Jilin University, Changchun, China. Data used to support the findings of this study are available from the corresponding author upon request.

Ethics and Consent Statement

Ethical approval was obtained by the ethics committee of the Ethics Review Board of the China-Japan Union Hospital of Jilin University.

Consent for Publication

A written permission for the use of patient data for publication was obtained.

Author Contributions

All authors made substantial contributions to acquisition of data, or analysis, conception and design, and interpretation of data; took part in drafting the article or revising it critically for important intellectual content; gave final approval of the version to be published; and agree to be accountable for all aspects of the work.

Funding

The authors declared that this case has received no financial support.

Disclosure

The authors declare that they have no competing interests.

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