Case Reports in Radiology
Volume 2015 (2015), Article ID 903150, 5 pages
http://dx.doi.org/10.1155/2015/903150

Case Report

Pseudoaneurysm of the Common Carotid Artery in an Infant due to Swallowed Fish Bone

Moulion Tapouh Jean Roger,¹ Fokou Marcus,² Fongang Emmanuel,³ Moifo Boniface,4,5 and Juimo Alain Georges3,4

¹Yaounde University Hospital Center, Yaounde, Cameroon
²Department of Surgery, Yaounde General Hospital, Yaounde, Cameroon
³Radiology Department, Yaounde General Hospital, Yaounde, Cameroon
⁴Faculty of Medicine and Biomedical Sciences (FMBS), Yaounde, Cameroon
⁵Radiology Department, Yaounde Gynaeco-Obstetric and Paediatric Hospital, Yaounde, Cameroon

Received 8 September 2015; Accepted 1 December 2015

Academic Editor: Atsushi Komemushi

Copyright © 2015 Moulion Tapouh Jean Roger et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

Abstract.

Carotid artery pseudoaneurysm is a rare condition, particularly in the paediatric population. Only about 30 cases of carotid artery aneurysms in infants have been published until now. This paper reports the case of a giant pseudoaneurysm of the left common carotid artery due to swallowed fish bone by an 8-year-old boy. This pseudoaneurysm was 5.5 cm transverse-diameter and resulted in severe respiratory distress. It was treated by resection and end-to-end anastomosis with satisfactory outcome after one-year follow-up. To the best of our knowledge, this is the largest carotid artery pseudoaneurysm ever described in children.

1. Introduction

Cervical masses in infants are frequent during routine clinical practice. They are usually congenital or of infectious origin and are often due to benign adenitis [1–3]. Vascular abnormalities, such as extracranial carotid aneurysms, are very uncommon. These aneurysms could be true aneurysms involving all the layers of the arterial wall or pseudoaneurysms in which there is no organic wall [4–6]. To our knowledge just about 30 cases of carotid artery aneurysms in infants have been published, a third of which were posttraumatic pseudoaneurysms which were either due to an accident or iatrogenic [5, 7, 8]. We report the case of an 8-year-old boy with no particular past history who underwent imaging for a suspected giant pseudoaneurysm of the left common carotid artery. This case is peculiar because of the exceptional aetiology which was the ingestion of an unnoticed fish bone.

2. Observation

An 8-year-old boy was investigated in the radiology department for a left-sided neck swelling which was observed 3 weeks earlier and was gradually increased in size. Physical examination revealed a painless pulsatile left-lateral cervical mass with a smooth outline, mild edema of the left hemiface, and a normal temperature. The infant looked generally well. A systolic murmur was present and suggestive of aneurysm. A contrast-enhanced computed tomography (CT) scan of the neck was performed (Figure 1) and showed a 42 mm × 55 mm × 28 mm ( × × AP) saccular dilatation of the left common carotid artery situated 20 mm proximally to the bifurcation. There was mass effect on adjacent structures notably the oesophagus and the trachea without significant stenosis. On reformatted images, a 45 mm long linear hyperdensity was depicted inside the aneurysm.

(a)

(b)

(c)

Figure 1: Axial (a) and coronal reformatted (b) contrast-enhanced CT scan images of the neck showing a saccular dilatation of the left common carotid artery with mass effect on the trachea and adjacent vascular structures. Axial bone window image (c) along the upper portion of the aneurysm shows a linear hyperdensity denoted with arrow-heads (later confirmed to be a fish bone).

The infant was admitted in the surgery department for a comprehensive preoperative work-up. A severe inspiratory dyspnea ensued which led to patient transfer to the intensive care unit where endotracheal intubation was performed. Heparin was administered and an emergency surgical operation was performed through a left posterior cleidomastoid incision, followed by clamping of the ipsilateral common, internal, and external carotid arteries. The aneurysmal sac was resected and a fish bone was found inside which had perforated the common carotid wall. An end-to-end anastomosis was carried out using Prolene 5/0 and cerebral blood-flow was reestablished. On day 2 after surgery there was complete regression of the dyspnea and one year later the patient was completely asymptomatic (Figure 2).

Figure 2: VRT CT picture at one-year follow-up. The common carotid is permeable without any residual dilation, with some mild scar narrowing at the anastomotic site (white arrow).

3. Discussion

Pseudoaneurysm is a hematoma that forms as the result of a leaking hole in an artery. It arises when a tear occurs in the arterial wall allowing blood to leak into the surrounding tissue, with persistent communication between the arterial lumen and the blood-filled cavity [9]. The main difference between true aneurysm and pseudoaneurysm is the lack of adventitia in pseudoaneurysm, where the whole wall is lacerated [8].

Pseudoaneurysms are particularly uncommon in the paediatric population. In a study of 57 659 infants with blunt trauma, Lew et al. reported only 15 cases (0.03%) of blunt carotid trauma [10] which are known to be potentially causative of pseudoaneurysms [11].

They generally are caused by direct arterial injury, which may result from trauma, vascular diagnostic or interventional procedures, adenotonsillectomy, and, in a lesser extent, deep infections [12]. Posttraumatic pseudoaneurysms of the carotid arteries are secondary to penetrating wounds or neck contusions. In these cases the tunica intima or media or the entire arterial wall is affected, resulting in extravasation into surrounding tissues [4, 7]. Iatrogenic pseudoaneurysms occur when the arterial wall is accidentally injured by a suture running too deeply [13] or a needle inserted for lymph node aspiration, for instance [9].

In our case, the child swallowed a fish bone two months before the cervical mass appeared. The fish bone perforated the wall of the oropharynx and injured the common carotid artery resulting in extravasation of blood into adjacent tissues. To our knowledge, this is the first report of a common carotid artery pseudoaneurysm resulting from food intake accident.

We found only 13 cases of noninfectious carotid pseudoaneurysms reported in the paediatric population from which 8 were iatrogenic (Table 1).

Table 1: Noninfectious carotid pseudoaneurysms reported in the paediatric population.

Authors and year
Sex and age
Carotid location
Mechanism
Treatment

Mahmoud et al., 2012 [8]
M, 4 years
Left common
Stabbing
Balloon trapping

Binning et al., 2010 [20]
F, 11 weeks
Right internal
Motor vehicle collision
Direct suture of the arterial defect and muslin sling wrapping

Singhal et al., 2009 [9]
M, 2 years
M, 8 years
Right internal
Fine needle aspiration of cervical lymph node
Proximal and distal coiling
Ligation

Beena et al., 2007 [7]
M, 3 years
Right internal
Needle aspiration of a parotid abscess
Not reported

DeFatta et al., 2005 [17]
F, 8 years
Left internal
Unclear : infection or transoral parapharyngeal abscess drainage
Ligation after coiling failure

Cuff and Thomas, 2005 [11]
M, 12 years
Left common
Elbow-strike during a basketball match
Resection and saphenous graft interposition

Hoff et al., 2005 [21]
M, 7 year
External
Tonsillectomy
Ligation

Chambers et al., 2002 [19]
F, 11 months
Right internal
Fall with a spoon inside the mouth
Coiling

Windfuhr, 2001 [15]
F, 5 years
Left internal
Fall with blunt trauma of head and neck
Ligation

Henriksen et al., 2000 [4]
F, 7 years
Right lateral aberrant internal
Myringotomy
Balloon embolization

Karas et al., 1997 [22]
M, 6 years
Right external
Tonsillectomy
Surgical trapping

Tovi et al., 1987 [13]
F, 14 years
Right internal
Tonsillectomy
Ligation of the sac with proximal and distal coiling

M: male. F: female.

The most common site of extracranial carotid artery pseudoaneurysms is the external carotid artery [5, 14] while aneurysms often involve the bifurcation of the common carotid artery. In this case, the pseudoaneurysm was located 20 mm proximal to the carotid bifurcation.

Extracranial carotid arteries aneurysms (either true or false) can be asymptomatic or present as a pulsating cervical mass [15]. This mass can compress the upper airways leading to dyspnoea [16] as in this case. Rarely, it can lead to a recurrent laryngeal nerve palsy [14], dysphagia, Horner syndrome, neck pain, or thromboembolic conditions (cerebral ischemia). Less frequent presentations include a mass mimicking a peritonsillar abscess, epistaxis, nasopharyngeal mass, paranasal sinus mass, and a pharyngeal mass [17]. The onset of neck pain should prompt the clinician to search for complications such as rupture, mural thrombosis, or dissection [5, 7].

The diagnosis of pseudoaneurysms may be made with Doppler ultrasonography, CT Angiography (CTA), magnetic resonance imaging (MRI), and angiography [5]. Conventional radiographs may show nonspecific findings like a homogeneous cervical opacity of water density with smooth outline that may be calcified. Doppler ultrasonography would confirm this to be of vascular origin and permit blood-flow assessment but it does not give sufficient information to plan management decision [18]. On CTA, pseudoaneurysm is a mass that is enhanced homogeneously in continuity with a blood vessel. This study will permit an assessment of surrounding structures. If thrombosis is present, there is a peripheral hypodense rim surrounding the blood that is flowing [14]. CTA is the preferred modality since it provides information about the feeding artery to the pseudoaneurysm, status of surrounding vessels and structures, and intracranial circulation. MRI, which is not necessary for the diagnosis, can enable visualisation of the pseudoaneurysm and thrombus if present and moreover permit a 3D rendering of the other arteries. Catheter angiography remains the gold standard for the diagnosis despite the fact that it is invasive. It is essential in determining the extent of a thrombus and the presence of arteriovenous fistulas and permits an assessment of collateral circulation [7, 15]. Usually, It is used when therapeutic procedures are being contemplated [9]. It has been recommended that duplex ultrasound could be used for neurologically asymptomatic patients and invasive angiography be reserved for those with deficits, evidence of vessel disruption, or abnormality on duplex scanning [11]. In our setting (low income country), only Doppler ultrasound and CTA are feasible, with the latter being less affordable because of its cost (at least 240 US $).

As stated by Singhal et al., the treatment of pseudoaneurysms depends on its morphology, the segment involved, the age of the patient, and most importantly the status of collateral circulation to brain [9]. However, the economic environment and the technical platform can seriously influence therapeutic choices. The primary goals of treatment are to isolate the pseudoaneurysm from circulation in order to prevent its rupture, to permit distal thromboembolism, and to relieve compression on adjacent vital structures [9].

Three therapeutic options could be considered in the treatment of carotid pseudoaneurysms: conservative management, endovascular treatment, or surgical repair. Conservative management with close long-term follow-up and anticoagulation should be reserved to very small aneurysms [15]. Endovascular treatment includes stent insertion and coiling and parent vessel occlusion. It can be efficiently used particularly when the cerebral circulation is satisfactory through the Willis circle [9, 12]. However, although several authors have already used endovascular treatment successfully [4, 8, 9, 19], it is not considered advisable on children because of insufficient data and some doubts about its long-term outcomes [5, 11]. In this case, surgical approach was chosen for two reasons. Firstly, there was a huge hematoma impairing airway that needed to be evacuated rapidly. The second reason was the level of the lesion, since common carotid artery is accessible to surgical approach without need to manipulate mandibular of other bones and nerves.

Surgical treatment includes five options summarized by Garg et al. [6]: clipping, resection and primary end-to-end anastomosis, resection with graft interposition, extracranial to intracranial bypass, and carotid artery ligation. Carotid artery ligation in children my cause stroke and possibly death if the collateral circulation is insufficient and should be reserved as last resort or in cases of aneurysm rupture. Restoring vascularization after surgical resection by direct anastomosis or bypass is the most recommended approach [5, 6, 13]. For lesions that are not accessible to surgical management, anticoagulation with or without stenting and close follow-up are appropriate [11]. Usually, anticoagulation is considered as a temporary treatment to reduce the embolic risk prior to surgery. The technique often used is resection of the pseudoaneurysm followed by end-to-end anastomosis or insertion of a venous graft [6]. In our case the end-to-end anastomosis was performed.

Several complications can follow the operation: transient ischemic attacks, stroke, cervical or cranial nerve injuries, graft occlusion, or death [5, 6]. Despite those complications, surgical management is the most frequently used option for the treatment of carotid pseudoaneurysm in children and is considered to have the better long-term prognosis. In 2007 Pourhassan et al. described 4 cases of surgically managed pseudoaneurysms in children with favourable outcome after 25-year follow-up [5].

4. Conclusion

Carotid artery pseudoaneurysm is an uncommon pathology particularly in the paediatric population. It is mostly due to trauma but can also occur during unexpected circumstances such as food intake. For the treatment, endovascular and surgical options could be considered, each possibility having its precise indications. When possible, surgical management by resection and end-to-end anastomosis would be preferred in order to avoid the risk of compression on neighbouring organs and rupture. This approach seems to provide the most favourable long-term outcome.

Conflict of Interests

The authors declare that there is no conflict of interests regarding the publication of this paper.

References

M. K. Badawy, “Pediatric neck masses,” Clinical Pediatric Emergency Medicine, vol. 11, no. 2, pp. 73–80, 2010.

M. R. Goins and M. S. Beasley, “Pediatric neck masses,” Oral and Maxillofacial Surgery Clinics of North America, vol. 24, no. 3, pp. 457–468, 2012.

E. R. Friedman and S. D. John, “Imaging of pediatric neck masses,” Radiologic Clinics of North America, vol. 49, no. 4, pp. 617–632, 2011.

S. D. Henriksen, M. W. Kindt, C. B. Pedersen, and H. J. Nepper-Rasmussen, “Pseudoaneurysm of a lateral internal carotid artery in the middle ear,” International Journal of Pediatric Otorhinolaryngology, vol. 52, no. 2, pp. 163–167, 2000.

S. Pourhassan, D. Grotemeyer, M. Fokou et al., “Extracranial carotid arteries aneurysms in children. Single-center experiences in 4 patients and review of the literature,” Journal of Pediatric Surgery, vol. 42, no. 11, pp. 1961–1968, 2007.

K. Garg, C. B. Rockman, V. Lee et al., “Presentation and management of carotid artery aneurysms and pseudoaneurysms,” Journal of Vascular Surgery, vol. 55, no. 6, pp. 1618–1622, 2012.

N. V. Beena, M. S. Kishore, A. Mahale, and V. Poornima, “Pseudoaneurysm of internal carotid artery,” Indian Journal of Pediatrics, vol. 74, no. 3, pp. 307–309, 2007.

M. Mahmoud, E. Roshdi, and D. Benderbous, “Traumatic pseudoaneurysms of the common carotid and vertebral artery in a four-year-old child,” Interventional Neuroradiology, vol. 18, no. 3, pp. 348–352, 2012.

M. Singhal, V. Gupta, P. Singh, A. Lal, A. Behra, and N. Khandelwal, “Iatrogenic life-threatening pseudoaneurysms of extracranial internal carotid artery after fine-needle aspiration of cervical Lymph nodes: report of two cases in children,” CardioVascular and Interventional Radiology, vol. 32, no. 6, pp. 1260–1263, 2009.

S. M. Lew, C. Frumiento, and S. L. Wald, “Pediatric blunt carotid injury: a review of the National Pediatric Trauma Registry,” Pediatric Neurosurgery, vol. 30, no. 5, pp. 239–244, 1999.

R. F. Cuff and J. H. Thomas, “Pediatric blunt carotid injury from low-impact trauma: a case report and review of the literature,” Journal of Trauma—Injury, Infection and Critical Care, vol. 58, no. 3, pp. 620–623, 2005.

U. Tannuri, N. Mendes De Almeida, R. Piske, and T. Matsumoto, “Giant pseudoaneurysm of the internal carotid artery causing upper airway obstruction in a 10-month-old infant treated by endovascular occlusion and surgical drainage,” Journal of Pediatric Surgery, vol. 38, no. 9, pp. 1393–1395, 2003.

F. Tovi, A. Leiberman, Y. Herizanu, and L. Golcman, “Pseudoaneurysm of the internal carotid artery secondary to tonsillectomy,” International Journal of Pediatric Otorhinolaryngology, vol. 13, no. 1, pp. 69–75, 1987.

W. Zamiati, M. I. Kably, and R. Kadiri, “A rare cause of recurrent laryngeal nerve palsy,” Journal de Radiologie, vol. 86, no. 9, part 1, pp. 1038–1039, 2005.

J. P. Windfuhr, “Aneurysm of the internal carotid artery following soft tissue penetration injury,” International Journal of Pediatric Otorhinolaryngology, vol. 61, no. 2, pp. 155–159, 2001.

N. De Luccia, E. S. da Silva, M. Aponchik, F. Appolonio, and L. A. Benvenuti, “Anévrysme congénital de l'artère carotide externe,” Annales de Chirurgie Vasculaire, vol. 24, no. 3, pp. 457.e7–457.e10, 2010.

R. J. DeFatta, D. J. Verret, and P. Bauer, “Extracranial internal carotid artery pseudoaneurysm,” International Journal of Pediatric Otorhinolaryngology, vol. 69, no. 8, pp. 1135–1139, 2005.

H. Constantinides, C. Passant, and A. N. Waddell, “Mycotic pseudoaneurysm of common carotid artery mimicking parapharyngeal abscess,” Journal of Laryngology and Otology, vol. 114, no. 10, pp. 796–797, 2000.

N. Chambers, D. Hampson-Evans, K. Patwardhan, and L. Murdoch, “Traumatic aneurysm of the internal carotid artery in an infant: a surprise diagnosis,” Paediatric Anaesthesia, vol. 12, no. 4, pp. 356–361, 2002.

M. J. Binning, R. Eskandari, and W. T. Couldwell, “Direct surgical repair of carotid pseudoaneurysm in an infant,” Child's Nervous System, vol. 26, no. 9, pp. 1151–1153, 2010.

M. Hoff, S. Graumüller, and H. W. Pau, “Arterial aneurysms as cause of gushing post-tonsillectomy hemorrhage,” Laryngo-Rhino-Otologie, vol. 84, no. 9, pp. 680–682, 2005.

D. E. Karas, R. S. Sawin, and K. C. Y. Sie, “Pseudoaneursym of the external carotid artery after tonsillectomy. A rare complication,” Archives of Otolaryngology—Head and Neck Surgery, vol. 123, no. 3, pp. 345–347, 1997.