<%server.execute "isdev.asp"%> Cervical and intracranial MRI findings in tetralogy of Fallot: Association with a persistent hypoglossal artery Mendes VC, Ferreira D, Figueiredo R, Dias Costa JM - J Pediatr Neurosci
home : about us : ahead of print : current issue : archives search instructions : subscriptionLogin 
Users online: 911      Small font sizeDefault font sizeIncrease font size Print this page Email this page


 
  Table of Contents    
LETTER TO THE EDITOR
Year : 2011  |  Volume : 6  |  Issue : 2  |  Page : 168-170
 

Cervical and intracranial MRI findings in tetralogy of Fallot: Association with a persistent hypoglossal artery


Department of Neuroradiology, Hospital de S. João, EPE, Porto, Portugal

Date of Web Publication13-Feb-2012

Correspondence Address:
Virgínia C Mendes
Serviço de Neurorradiologia, Hospital de S. João, Alameda Professor Hernâni Monteiro, 4000 - Porto
Portugal
Login to access the Email id

Source of Support: None, Conflict of Interest: None


DOI: 10.4103/1817-1745.92867

Rights and Permissions

 



How to cite this article:
Mendes VC, Ferreira D, Figueiredo R, Dias Costa JM. Cervical and intracranial MRI findings in tetralogy of Fallot: Association with a persistent hypoglossal artery. J Pediatr Neurosci 2011;6:168-70

How to cite this URL:
Mendes VC, Ferreira D, Figueiredo R, Dias Costa JM. Cervical and intracranial MRI findings in tetralogy of Fallot: Association with a persistent hypoglossal artery. J Pediatr Neurosci [serial online] 2011 [cited 2019 Jul 18];6:168-70. Available from: http://www.pediatricneurosciences.com/text.asp?2011/6/2/168/92867


Dear Sir,

Persistent primitive hypoglossal artery (PHA) is a rare embryonic carotid-basilar artery anastomosis, demonstrated in about 0.027-0.26% of cerebral angiograms. [1],[2] Furthermore, the PHA is often functionally a single artery or the most prominent supply to the brainstem and cerebellum. [1]

Tetralogy of Fallot (TOF) is the most common cyanotic cardiac defect, with a classic tetrad of manifestations: Pulmonary outflow tract stenosis or atresia, ventricular septal defect, aortic override, and right ventricular hypertrophy. [3]

We describe an extremely rare combination of TOF associated with a right aortic arch with a mirror-image branching, and a persistent hypoglossal artery.

A 2-year-old boy was admitted at our radiological department with visual impairment after being submitted to an elective surgical repair with Goretex graft interposed between the pulmonary artery and the brachiocephalic trunk. He was diagnosed with TOF at 25 gestational weeks and undergone surgical repair at day 7 of life. The deletion 22q11 was negative. His daily activity and neurological development were fair, but he presented with hypotonia and was speechless.

Brain magnetic resonance imaging (MRI) showed small dot-like lesions supra- and infratentorial with hyposignal on T2 gradient eco-weighted images [Figure 1] suggesting microbleeds due to microemboli. Contrast enhanced MRA demonstrated a right aortic arch with mirror-image branching and an anomalous vessel arising from the right internal carotid at the C2-C3 level and leading to the basilar artery [Figure 2]. Imaging of the time of flights revealed that this vessel entered the skull through the hypoglossal canal [Figure 3]. Bilateral vertebral arteries were hypoplastic, but the right posterior communicating artery was present.
Figure 1: Axial T2* gradient eco-weighted images showing brain microbleeds, appearing as small dots-like foci with hyposignal

Click here to view
Figure 2: Coronal and sagital imaging in contrast enhanced MRA showing an anomalous vessel arising from the right internal carotid artery to the basilar artery. In addition, a right aortic arch with a mirror– image branching is also demonstrated

Click here to view
Figure 3: Axial source image from 3D-TOF MRA demonstrating an anomalous artery coursing through the right hypoglossal canal to form the basilar artery with hypoplastic vertebral arteries

Click here to view


The patient condition slowly improved, and was discharged from the hospital with regular follow-ups at our pediatric cardiology department.

Neurological and developmental deficits are common in children with congenital heart disease due to multiple factors that include the etiology of the congenital heart disease, the effects of abnormal cardiovascular function, and the possible sequelae of open-heart surgery. Perioperative neurological complications include diffuse hypoxic-ischemic injury, cerebral hemorrhage, focal infarction due to macroemboli, but a leading cause of neurocognitive defects associated with open cardiac surgery is the production and circulation of microemboli. [4] The major types of microemboli are gas emboli, foreign material, and emboli generated from blood elements.

The PHA is a vestige of the embryonic carotid-vertebrobasilar anastomoses present during the 4-5 mm embryo stage. The embryological explanation begins with the description of two cerebral arterial systems present in the early development. The anterior one gives rise to the carotid artery which develops as a cranial extension of the paired dorsal aorta, and the posterior is the longitudinal neural artery. At the 3-4 mm stage, anastomotic vessels between the internal carotid artery and the longitudinal neural artery compensate for the absence of the vertebral arteries. These vessels are later known as carotid-vertebrobasilar anastomoses and are named after the cranial nerves with which they run. The hypoglossal arteries are formed by the second pair of segmental arteries. The anastomosis between the longitudinal neural arteries gives rise to the basilar artery. This artery then joins the internal carotid artery via the posterior communicating artery. At this time (5-6 mm stage) the otic, hypoglossal, and trigeminal arteries start to regress. [5]

Developmental anomalies of the aortic arch vessels are well known. About 25% of patients with TOF have a right aortic arch, most often with mirror-image branching. [2] The aortic arch anomalies can be understood by their embryologic origins. Development of the aortic arch can be described by the appearance and persistence or dissolution of the six paired vessels connecting the truncoaortic sac of the embryonic heart tube with the paired dorsal aortae. [6] When the right dorsal aorta remains patent and either the left fourth arch or the left dorsal aorta regresses abnormally, the right aortic arch is formed. If the distal portion of the left aortic arch, adjacent to the descending aorta, disappears, the subsequent developmental process results in a mirror image of the normal process. [7]

With the exception of atrial septal defect previously described in two case reports, [8],[9] however, anomalies of the heart and aortic arch vessels in combination with PHA have never been reported. Our case, which illustrates the coexistence of a TOF and PHA, is to our knowledge the first reported case in the English language literature.

The coexistence of these vascular anomalies in the patient raises the question of a common etiologic factor or factors in their pathogenesis. One possible explanation for the persistent hypoglossal artery being frequently associated with hypoplastic vertebral arteries is the less need of vertebral arteries to supply the posterior circulation and the brainstem. It is difficult to relate the TOF and the right aortic arch associated with mirror-image branching with a persistent hypoglossal artery, but we can presume a common embryonic insult at the 3-10 mm fetal stage.

 
   References Top

1.Baltsavias GM, Chourmouzi D, Tasianas N, Drevelengas A, Damianovski D, Jovkovski S. Ruptured aneurysm of a persistent primitive hypoglossal artery (PHA) treated by endovascular approach-Case report and literature review. Surg Neurol 2007;68:338-43.  Back to cited text no. 1
[PUBMED]  [FULLTEXT]  
2.Meguro T, Terada K, Hirotsune N, Nishino S, Asano T. Unusual variant of persistent primitive hypoglossal artery. Br J Radiol 2007;80: e314-6.  Back to cited text no. 2
[PUBMED]  [FULLTEXT]  
3.Frank L, Dillman JR, Parish V, Mueller GC, Kazerooni EA, Bell A, et al. Cardiovascular MR imaging of conotruncal anomalies. RadioGraphics 2010;30:1069-94.  Back to cited text no. 3
    
4.Miller G, Vogel H. Structural evidence of injury or malformation in the brains of children with congenital heart disease. Semin Pediatr Neurol 1999;6:20-6.  Back to cited text no. 4
[PUBMED]    
5.Lee EJ, Chang HW, Cho CH, Kim E, Lee SK, Kwon JH. Rare variant of persistent primitive hypoglossal artery in magnetic resonance angiography. Surg Radiol Anat 2010;32:801-4.  Back to cited text no. 5
[PUBMED]  [FULLTEXT]  
6.Chang HK, Wang JN, Hung WP, Chen SJ, Wu JM. Tetralogy of Fallot associated with right arch and persistent left dorsal aortic aneurysm. Int J Cardiol 2011;149: e53-4.  Back to cited text no. 6
[PUBMED]  [FULLTEXT]  
7.Higashikuni Y, Nagashima T, Ishizaka N, Kinugawa K, Hirata Y, Nagai R. Right aortic arch with mirror image branching and vascular ring. Int J Cardiol 2008;130: e53-5.  Back to cited text no. 7
[PUBMED]  [FULLTEXT]  
8.Komaba Y, Nomoto T, Hiraide T, Kitamura S, Terashi A. Persistent primitive hypoglossal artery complicated by atrial septal defect and congenital intrahepatic shunts. Intern Med 1998;37:60-  Back to cited text no. 8
    
9.Matsui H, Udaka F, Kubori T, Oda M, Nishinaka K, Kameyama M. Persistent primitive hypoglossal artery with atrial septal defect. Intern Med 2005;44:507-8.  Back to cited text no. 9
[PUBMED]  [FULLTEXT]  


    Figures

  [Figure 1], [Figure 2], [Figure 3]



 

Top
Print this article  Email this article
 
 
  Search
 
  
 
    Similar in PUBMED
   Search Pubmed for
   Search in Google Scholar for
    Article in PDF (433 KB)
    Citation Manager
    Access Statistics
    Reader Comments
    Email Alert *
    Add to My List *
* Registration required (free)  


    References
    Article Figures

 Article Access Statistics
    Viewed2334    
    Printed53    
    Emailed0    
    PDF Downloaded71    
    Comments [Add]    

Recommend this journal