Hindawi Publishing Corporation Case Reports in Medicine Volume 2013, Article ID 209767, 3 pages http://dx.doi.org/10.1155/2013/209767 Case Report Bilateral Intracavernous Carotid Artery Aneurysms Presenting as Diplopia in a Young Patient Nikolaos Kopsachilis, 1 Maria Pefkianaki, 1 Gianluca Carifi, 1 and Ioannis Lialias 2 1 Moorfields Eye Hospital, London EC1V 2PD, UK 2 Aristotle University of essaloniki, essaloniki, Greece Correspondence should be addressed to Nikolaos Kopsachilis; [email protected] Received 11 November 2012; Revised 26 January 2013; Accepted 17 February 2013 Academic Editor: Murat Ugurlucan Copyright © 2013 Nikolaos Kopsachilis et al. is 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. Introduction. Bilateral intracavernous carotid artery aneurysms (ICAAs) are extremely rare and difficult to treat. Case Report.A 26-year-old female presented in our clinic with acute diplopia due to oculomotor nerve palsy on the leſt side. Magnetic resonance imaging of the brain showed two heterogeneously enhanced masses indicating bilateral ICAA. An endovascular coil embolization was performed on the leſt side successfully, resulting in resolution of her symptoms. Conclusion. orough systemic evaluation in young patients with diplopia can reveal life-threatening underlying pathology and prevent major complications. 1. Introduction Artery aneurysms are found in 5% of the general population and become symptomatic in 9/100.000, most frequently in the fiſth and sixth decades of life [1]. Intracavernous carotid artery aneurysms (ICAAs) represent less than 1% of intracra- nial aneurysms and show a slight female predominance [2]. Bilateral intracavernous carotid artery aneurysms are extremely rare and difficult to treat. We report an unusual case of bilateral ICAA in a very young female patient presented as acute diplopia and treated with endovascular coil embolization. 2. Case Report A 26-year-old woman was referred to our clinic with transient worsening diplopia. She also complained of headaches and had no further general motor or sensory symptoms. e patient had no history of hypertension or hypercholes- terolemia and was not on any medications. Visual acuity was 6/5 in the right eye and 6/6 in the leſt eye. Intraocular pressures were 13 mm Hg both sides. Slit lamp examination was normal, and fundoscopy findings were unremarkable in both eyes. Orthoptic examination showed oculomotor nerve palsy on the leſt side. Other cranial nerves including abducens and trochlear nerves were intact. No systemic diseases such as Ehlers-Danlos, Paget’s disease, or Marfan’s syndrome were recorded. With regard to the clinical findings, magnetic resonance imaging (MRI) of the brain was scheduled. Coronal and axial T 1 weighted images demonstrated two heterogeneously enhanced masses indicating bilateral ICCA (Figure 1). Bilat- eral internal carotid arteries were visualized as flow voids encircling the mass. An endovascular coil embolization using a Guglielmi detachable microcoil was performed on the leſt side unevent- fully, in our Department of Neuroradiology. e patient tolerated the procedure well, and there were no major post- operative complications. A postoperative MRI scan showed successful thrombosis of the leſt aneurysm (Figure 2). One month aſter embolization, her diplopia had completely resolved. In view of the good postoperative result, an identical procedure on the right side was performed uneventfully 3 months later. At 6 months aſter initial presentation, the patient had recovered completely and had no recurrence of her diplopia.
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Hindawi Publishing CorporationCase Reports in MedicineVolume 2013, Article ID 209767, 3 pageshttp://dx.doi.org/10.1155/2013/209767
Case ReportBilateral Intracavernous Carotid Artery AneurysmsPresenting as Diplopia in a Young Patient
Nikolaos Kopsachilis,1 Maria Pefkianaki,1 Gianluca Carifi,1 and Ioannis Lialias2
1 Moorfields Eye Hospital, London EC1V 2PD, UK2Aristotle University of Thessaloniki, Thessaloniki, Greece
Correspondence should be addressed to Nikolaos Kopsachilis; [email protected]
Received 11 November 2012; Revised 26 January 2013; Accepted 17 February 2013
Academic Editor: Murat Ugurlucan
Copyright © 2013 Nikolaos Kopsachilis et al. This is an open access article distributed under the Creative Commons AttributionLicense, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properlycited.
Introduction. Bilateral intracavernous carotid artery aneurysms (ICAAs) are extremely rare and difficult to treat. Case Report. A26-year-old female presented in our clinic with acute diplopia due to oculomotor nerve palsy on the left side. Magnetic resonanceimaging of the brain showed two heterogeneously enhanced masses indicating bilateral ICAA. An endovascular coil embolizationwas performed on the left side successfully, resulting in resolution of her symptoms. Conclusion. Thorough systemic evaluation inyoung patients with diplopia can reveal life-threatening underlying pathology and prevent major complications.
1. Introduction
Artery aneurysms are found in 5% of the general populationand become symptomatic in 9/100.000, most frequently inthe fifth and sixth decades of life [1]. Intracavernous carotidartery aneurysms (ICAAs) represent less than 1% of intracra-nial aneurysms and show a slight female predominance[2]. Bilateral intracavernous carotid artery aneurysms areextremely rare and difficult to treat.
We report an unusual case of bilateral ICAA in a veryyoung female patient presented as acute diplopia and treatedwith endovascular coil embolization.
2. Case Report
A26-year-oldwomanwas referred to our clinicwith transientworsening diplopia. She also complained of headaches andhad no further general motor or sensory symptoms. Thepatient had no history of hypertension or hypercholes-terolemia and was not on any medications. Visual acuitywas 6/5 in the right eye and 6/6 in the left eye. Intraocularpressures were 13mmHg both sides. Slit lamp examinationwas normal, and fundoscopy findings were unremarkable in
both eyes. Orthoptic examination showed oculomotor nervepalsy on the left side.Other cranial nerves including abducensand trochlear nerves were intact. No systemic diseases suchas Ehlers-Danlos, Paget’s disease, or Marfan’s syndrome wererecorded.
With regard to the clinical findings, magnetic resonanceimaging (MRI) of the brain was scheduled. Coronal andaxial T
1weighted images demonstrated two heterogeneously
enhanced masses indicating bilateral ICCA (Figure 1). Bilat-eral internal carotid arteries were visualized as flow voidsencircling the mass.
An endovascular coil embolization using a Guglielmidetachable microcoil was performed on the left side unevent-fully, in our Department of Neuroradiology. The patienttolerated the procedure well, and there were no major post-operative complications. A postoperative MRI scan showedsuccessful thrombosis of the left aneurysm (Figure 2). Onemonth after embolization, her diplopia had completelyresolved. In view of the good postoperative result, an identicalprocedure on the right side was performed uneventfully3 months later. At 6 months after initial presentation, thepatient had recovered completely and had no recurrence ofher diplopia.
2 Case Reports in Medicine
(a) (b)
Figure 1: T1weightedMRl of coronal (a) and (b) axial slices in a 26-year-old patient with transient diplopia and oculomotor nerve palsy on the
left side. Two heterogeneously enhancedmasses and an enhanced thin outermembrane can be recognized, indicating bilateral intracavernouscarotid artery aneurysms.
(a) (b)
Figure 2: T1weighted MRl axial slices of the same patient 2 days after treatment of the left intracavernous carotid artery aneurysm with
endovascular coil embolization (a). Note the slight hypointensity due to thrombosis in the region of the previous left aneurysm (b).
3. Discussion
The etiology of giant aneurysms is multifactorial and manystructural and hemodynamic stress factors have been pre-viously discussed. However, pathogenesis of the cavernousaneurysm is not yet defined, and idiopathic intracavernousaneurysms are the most common [3].
Many bilateral intracavernous aneurysm cases have def-inite causative factors suggesting weakness of the carotidarterial wall. They can occur after radiation therapy or inassociation with connective tissue disorders such as fibro-muscular dysplasia and Paget’s Disease [4]. Furthermore,infectious (mycotic and bacterial) intracavernous aneurysmshave been reported in the past [5].
The likelihood of an aneurysm becoming symptomaticis directly related to its size. The most common cause ofsymptoms (90%) is rupture which can result in severe sub-arachnoid hemorrhage. Symptoms start with diplopia, photo-phobia nausea, and vomiting following respiratory arrest witha 50% death ratio. Rupture can also result in arteriovenous
fistula or posterior fossa hematoma. In addition, stroke-likesymptoms can be created by thrombosis. If the aneurysmis large enough, it compresses surrounding structures andcauses progressive neuropathy. In this situation, the symp-toms are progressive and less resulting in visual loss, diplopia,ptosis, and other focal deficits. The symptoms are directlyrelated to the cranial nerves (III, IV,VI, VII, andVI) that crossthe cavernous sinus [5].
Optimalmanagement of symptomatic giant carotid aneu-rysms remains controversial. However, present treatmentoptions favor bypass or embolization to direct surgery withvery good results, as in our case [6].
To summarize we report an interesting case of bilateralICAA in 26-year-old female presented as acute diplopia andemphasize the need of a thorough systemic evaluation inyoung patients with diplopia.
Conflict of Interests
The authors declare no conflict of interests.
Case Reports in Medicine 3
References
[1] V. A. Purvin, “Neuro-ophthalmic aspects of aneurysms,” Inter-national Ophthalmology Clinics, vol. 49, no. 3, pp. 119–132, 2009.
[2] M. E. Linskey, L. N. Sekhar, W. Hirsch Jr., H. Yonas, and J.A. Horton, “Aneurysms of the intracavernous carotid artery:clinical presentation, radiographic features, and pathogenesis,”Neurosurgery, vol. 26, no. 1, pp. 71–79, 1990.
[3] L.N. Sekhar,D. Ramanathan,D.K.Hallam, B.V.Ghodke, andL.J. Kim, “What is the correct approach to aneurysmmanagementin 2011?”World Neurosurgery, vol. 75, no. 3-4, pp. 409–411, 2011.
[4] T. Rehman, R. Ali, C. Taylor, and H. Yonas, “Bilateral giantcavernous carotid artery aneurysms in a child with juvenilePaget’s disease,”World Neurosurgery, vol. 73, no. 6, pp. 691–693,2010.
[5] B. R. Seo, T. S. Kim, S. P. Joo, and S. I. Jung, “Endovascular treat-ment of infective aneurysms of the bilateral cavernous sinus:case report and reviewof the literature,”ClinicalNeuroradiology,vol. 19, no. 2, pp. 162–165, 2009.
[6] J. M. Zabramski, R. F. Spetzler, and C. G. McDougall, “Percu-taneous intracranial stent placement for aneurysms,” Journal ofNeurosurgery, vol. 99, no. 1, pp. 23–30, 2003.
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