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DOI: 10.1055/s-0045-1811243
Clinical Features and Post-Coiling Outcomes of Symptomatic Internal Carotid Artery–Posterior Communicating Artery Aneurysms: A Case Series and Literature Review
Funding None.
Abstract
Objective
This article aims to understand the clinical course of symptomatic internal carotid artery (ICA)–posterior communicating artery (PCom) aneurysms and the outcomes of post-coiling for unruptured symptomatic aneurysms by analyzing the anatomical imaging data and patient backgrounds of patients treated in our institute in the last 5 years.
Materials and Methods
This study enrolled 82 patients with ICA-PCom aneurysms. Anatomical factors, including age, sex, side, aneurysm dome and neck size, aneurysm depth/neck width ratio (ASPECT ratio), family history of cerebral aneurysm, history of hypertension, smoking habit, angle between aneurysm dome protrusion and ICA C2 portion, angle between ICA C2 and C3 portions, and PCom diameter, were analyzed. In the outcome analysis of coil embolization for symptomatic unruptured ICA-PCom aneurysms, we evaluated age, sex, side, aneurysm dome and neck side, ASPECT ratio, volume embolization ratio, and time from onset.
Statistical Analysis
Mann–Whitney U and Fisher's exact tests were utilized for quantitative and categorical variables, respectively.
Results
In both ruptured and unruptured ICA-PCom aneurysms, the angle between the aneurysm dome protrusion and ICA C2 portion and the angle between the ICA C2 and C3 portions were smaller in the oculomotor palsy group than in the nonoculomotor palsy group. Other factors such as age, sex, side, aneurysm dome, neck, ASPECT ratio, family history, hypertension, smoking, and PCom diameter did not significantly influence oculomotor palsy. Early coil embolization led to better recovery of neural function, with immediate intervention offering the highest chance of full recovery.
Conclusion
Overall, this study showed that sharp ICA siphon and aneurysm dome protrusion are significant factors in symptomatic ICA-PCom aneurysms. We propose that immediate surgery be recommended for patients with ICA-PCom aneurysm-induced oculomotor nerve palsy to prevent functional disability and potential aneurysm rupture.
Keywords
internal carotid artery–posterior communicating artery aneurysm - internal carotid artery siphon - aneurysm dome protrusion - oculomotor nerve palsy - angleIntroduction
Oculomotor nerve palsy caused by an internal carotid artery (ICA)–posterior communicating artery (PCom) aneurysm is a well-known clinical condition. Direct mechanical compression can cause partial or complete oculomotor palsy. Herein, we assessed the radiological image findings and patient demographics associated with symptomatic ICA-PCom aneurysms, reviewing the anatomical imaging findings, patient demographics, and clinical backgrounds of symptomatic ICA-PCom aneurysm cases over a period of 5 years. Additionally, we assessed the outcomes following endovascular coiling of symptomatic unruptured aneurysms.
Materials and Methods
Patient Selection and Study Period
Between April 2019 and March 2024, 82 patients with ICA-PCom aneurysms underwent surgical treatment at our institute, among whom 12 had a history of oculomotor palsy symptoms, while 7 symptomatic unruptured aneurysms were treated with coil embolization.
Imaging and Anatomical Analysis
All patients underwent digital subtraction angiography for aneurysm analysis. ICA-PCom aneurysms were analyzed using internal carotid angiography (ICAG), and the angles between the parent artery and aneurysm and between the ICA C2 portion and C3 portion were measured in the lateral view of the ICAG.
The following parameters were assessed: age, sex, side, aneurysmal dome size and neck, family history of cerebral aneurysm, history of hypertension, smoking habit ([Fig. 1A], [D]), the angle between the direction of protrusion of the aneurysm dome and the direction of the parent artery (ICA C2 portion) ([Fig. 1B], [D]), the angle between the ICA C2 and C3 portions (the angle between the ICA C2 portion [the line crossing the center point of C2 and the bottom point of C2, shown with white dots] and C3 portion [the line crossing the center point of C3 and the bottom point of C2, shown with white dots]) ([Fig. 1C]), the angle between the direction of protrusion of the aneurysm dome (the line along both the top point of the aneurysm dome and the center point of the aneurysm dome, shown with white dots) and the ICA C2 portion (the line crossing the center point of C2 and the bottom point of C2, shown with white dots), aneurysm depth/neck width ratio (ASPECT ratio), and PCom artery diameter ([Fig. 1F]).


Statistical Analysis
The Mann–Whitney U test was used for quantitative variables to assess the differences in the estimated data between the groups. Fisher's exact test was used for categorical variables. Results were considered significant at p < 0.05.
Results
Clinical Characteristics and Radiological Findings of Unruptured Symptomatic ICA-PCom Aneurysms
There were significant differences between unruptured ICA-PCom aneurysms in the palsy and non-palsy groups in the angle between the direction of protrusion of the aneurysm dome and the direction of the ICA C2 portion (47.5 ± 7.86 vs. 100.8 ± 29.0, p = 0.001), and the angle between ICA C2 and C3 portions (37.5 ± 8.86 vs. 77.6 ± 17.5, p = 0.047). There were no significant differences in other factors ([Table 1]).
Abbreviations: ASPECT ratio, aneurysm depth/neck width ratio; ICA, internal carotid artery; PCom, posterior communicating artery; SD, standard deviation.
Clinical Characteristics and Radiological Findings of Ruptured Symptomatic ICA-PCom Aneurysms
There were significant differences between ruptured ICA-PCom aneurysms in the palsy and nonpalsy groups in the angle between the direction of protrusion of the aneurysm dome and the direction of the ICA C2 portion (50.5 ± 3.54 vs. 97.4 ± 17.1, p = 0.004), and the angle between ICA C2 and C3 portions (31.0 ± 5.66 vs. 76.1 ± 13.5, p = 0.042). There were no significant differences in other factors ([Table 2]).
Abbreviations: ASPECT ratio, aneurysm depth/neck width ratio; ICA, internal carotid artery; PCom, posterior communicating artery; SD, standard deviation.
Outcome analysis of Post-Coiling for Symptomatic Unruptured ICA-PCom Aneurysms
When comparing outcomes in post-coiling for symptomatic unruptured ICA-PCom aneurysms, patients who improved had significantly smaller aneurysm domes (5.424 ± 1.05 vs. 10.79 ± 2.11 mm, p = 0.021) and significantly fewer days from onset (0.23 ± 0.41 vs. 2.5 ± 1.33 days, p = 0.013). There were no significant differences in other factors ([Table 3]).
Abbreviations: ASPECT ratio, aneurysm depth/neck width ratio; ICA, internal carotid artery; PCom, posterior communicating artery; SD, standard deviation; VER, volume embolization ratio.
Ruptured Symptomatic ICA-PCom Aneurysms
In our series, there were only two cases of ruptured symptomatic ICA-PCom aneurysms. In one case, the patient was in Hunt and Kosnik grade 1. Coil embolization was performed on the day of onset, and oculomotor palsy was completely resolved. In another case, the patient was in Hunt and Kosnik grade 4, and coil embolization was performed on the day of onset; however, the oculomotor palsy and severe conscious disturbance did not resolve.
Discussion
In previous studies,[1] [2] [3] [4] 7 to 10% of patients with unruptured ICA-PCom aneurysms exhibited oculomotor nerve palsy, and the association between ruptured ICA-PCom aneurysms and the onset of oculomotor nerve palsy was reported to be 34 to 56%.[2] [3] [4] In our series, 14.3% of patients with unruptured ICA-PCom aneurysms exhibited oculomotor nerve palsy.
In addition, previous studies[4] [5] reported that symptomatic ICA-PCom aneurysms tend to be larger and more irregularly shaped than asymptomatic ICA-PCom aneurysms. In our cases, there were no significant differences in aneurysms size.
In contrast, there were no significant aneurysm dome or neck differences between symptomatic and asymptomatic aneurysms in our cases. Another factor associated with symptomatic ICA-PCom aneurysms is ICA tortuosity. A short ICA and sharp ICA siphon may cause a short distance between the skull base and ICA.[6] Almost all projections of symptomatic PCom aneurysms, which cause oculomotor palsy, protruding from the ICA are ventral, lateral, and posterior.[4] [5] [6] In addition, such aneurysms measuring smaller than 1 cm can cause third nerve palsy when the anterior cavernous genu of the ICA forms an acute angle and the supraclinoid portion runs posterolaterally,[4] [5] [6] while the PCom is of the fetal type.[7] In our cases, a sharp ICA siphon and protruding aneurysm dome were identified as significant factors influencing symptomatic ICA-PCom aneurysm. We assume this “sharp ICA siphon and protruding aneurysm dome” directly compresses the oculomotor nerve as in [Fig. 2].


Oculomotor nerve disturbance can be caused by compression from an enlarging aneurysm[8] and by the irritant effect of an aneurysm.[9] However, previous reports have emphasized that both coil embolization and neck clipping for such symptomatic ICA-PCom aneurysms could ensure recovery from oculomotor nerve palsy.[10] [11] As endovascular coiling does not reduce the aneurysm mass, the possible mechanism of aneurysm-induced oculomotor palsy can be explained by pulsation stress on the oculomotor nerve and not solely by compression of the nerve.
In our case series, symptomatic ICA-PCom aneurysms were treated with coil embolization. In two ruptured cases, one had a good outcome, achieving complete resolution of oculomotor palsy after coil embolization, whereas the other case had a poorer outcome because the patient's initial Hunt and Kosnik grade was poor. Patients with unruptured ICA-PCom aneurysms who underwent coil embolization immediately after onset had good outcomes.
Timely surgical intervention is an important factor for complete oculomotor nerve recovery in both ruptured and unruptured aneurysms.[4] [8] [12] [13] In our study, immediate coil embolization for unruptured aneurysms could ensure complete oculomotor nerve recovery. Other factors, such as age, aneurysm dome and neck size, and volume embolization ratio, were not predictive of recovery from oculomotor nerve palsy. Consequently, we suggest performing immediate surgery for ICA-PCom aneurysm-induced oculomotor nerve palsy to prevent functional disability and potential aneurysm rupture.
Conclusion
To conclude that a sharp ICA siphon and protruding aneurysm dome are significant factors for symptomatic ICA-PCom aneurysms. In addition, we recommend immediate surgery for ICA-PCom aneurysm-induced oculomotor nerve palsy to prevent functional disability and potential aneurysm rupture.
Conflict of Interest
None declared.
Ethical Approval
This study was approved by our institutional review board.
Data Availability Statement
This study data is unavailable to access or unsuitable to post, because this research data includes sensitive or confidential information such as patient data.
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References
- 1 Friedman JA, Piepgras DG, Pichelmann MA, Hansen KK, Brown Jr RD, Wiebers DO. Small cerebral aneurysms presenting with symptoms other than rupture. Neurology 2001; 57 (07) 1212-1216
- 2 Hamilton JG, Falconer MA. Immediate and late results of surgery in cases of saccular intracranial aneurysms. J Neurosurg 1959; 16: 514-541
- 3 Paterson A. Direct surgery in the treatment of posterior communicating aneurysms. Lancet 1968; 2 (7572): 808-811
- 4 Soni SR. Aneurysms of the posterior communicating artery and oculomotor paresis. J Neurol Neurosurg Psychiatry 1974; 37 (04) 475-484
- 5 Lv N, Yu Y, Xu J, Karmonik C, Liu J, Huang Q. Hemodynamic and morphological characteristics of unruptured posterior communicating artery aneurysms with oculomotor nerve palsy. J Neurosurg 2016; 125 (02) 264-268
- 6 Anan M, Nagai Y, Fudaba H. et al. Third nerve palsy caused by compression of the posterior communicating artery aneurysm does not depend on the size of the aneurysm, but on the distance between the ICA and the anterior-posterior clinoid process. Clin Neurol Neurosurg 2014; 123: 169-173
- 7 González-Darder JM, Quilis-Quesada V, Talamantes-Escribá F, Botella-Maciá L, Verdú-López F. Microsurgical relations between internal carotid artery-posterior communicating artery (ICA-PComA) segment aneurysms and skull base: an anatomoclinical study. J Neurol Surg B Skull Base 2012; 73 (05) 337-341
- 8 Giombini S, Ferraresi S, Pluchino F. Reversal of oculomotor disorders after intracranial aneurysm surgery. Acta Neurochir (Wien) 1991; 112 (1-2): 19-24
- 9 Lanzino G, Andreoli A, Tognetti F. et al. Orbital pain and unruptured carotid-posterior communicating artery aneurysms: the role of sensory fibers of the third cranial nerve. Acta Neurochir (Wien) 1993; 120 (1-2): 7-11
- 10 Birchall D, Khangure MS, McAuliffe W. Resolution of third nerve paresis after endovascular management of aneurysms of the posterior communicating artery. AJNR Am J Neuroradiol 1999; 20 (03) 411-413
- 11 Chalouhi N, Theofanis T, Jabbour P. et al. Endovascular treatment of posterior communicating artery aneurysms with oculomotor nerve palsy: clinical outcomes and predictors of nerve recovery. AJNR Am J Neuroradiol 2013; 34 (04) 828-832
- 12 Fujiwara S, Fujii K, Nishio S, Matsushima T, Fukui M. Oculomotor nerve palsy in patients with cerebral aneurysms. Neurosurg Rev 1989; 12 (02) 123-132
- 13 Leivo S, Hernesniemi J, Luukkonen M, Vapalahti M. Early surgery improves the cure of aneurysm-induced oculomotor palsy. Surg Neurol 1996; 45 (05) 430-434
Address for correspondence
Publikationsverlauf
Artikel online veröffentlicht:
21. August 2025
© 2025. Asian Congress of Neurological Surgeons. This is an open access article published by Thieme under the terms of the Creative Commons Attribution-NonDerivative-NonCommercial License, permitting copying and reproduction so long as the original work is given appropriate credit. Contents may not be used for commercial purposes, or adapted, remixed, transformed or built upon. (https://creativecommons.org/licenses/by-nc-nd/4.0/)
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References
- 1 Friedman JA, Piepgras DG, Pichelmann MA, Hansen KK, Brown Jr RD, Wiebers DO. Small cerebral aneurysms presenting with symptoms other than rupture. Neurology 2001; 57 (07) 1212-1216
- 2 Hamilton JG, Falconer MA. Immediate and late results of surgery in cases of saccular intracranial aneurysms. J Neurosurg 1959; 16: 514-541
- 3 Paterson A. Direct surgery in the treatment of posterior communicating aneurysms. Lancet 1968; 2 (7572): 808-811
- 4 Soni SR. Aneurysms of the posterior communicating artery and oculomotor paresis. J Neurol Neurosurg Psychiatry 1974; 37 (04) 475-484
- 5 Lv N, Yu Y, Xu J, Karmonik C, Liu J, Huang Q. Hemodynamic and morphological characteristics of unruptured posterior communicating artery aneurysms with oculomotor nerve palsy. J Neurosurg 2016; 125 (02) 264-268
- 6 Anan M, Nagai Y, Fudaba H. et al. Third nerve palsy caused by compression of the posterior communicating artery aneurysm does not depend on the size of the aneurysm, but on the distance between the ICA and the anterior-posterior clinoid process. Clin Neurol Neurosurg 2014; 123: 169-173
- 7 González-Darder JM, Quilis-Quesada V, Talamantes-Escribá F, Botella-Maciá L, Verdú-López F. Microsurgical relations between internal carotid artery-posterior communicating artery (ICA-PComA) segment aneurysms and skull base: an anatomoclinical study. J Neurol Surg B Skull Base 2012; 73 (05) 337-341
- 8 Giombini S, Ferraresi S, Pluchino F. Reversal of oculomotor disorders after intracranial aneurysm surgery. Acta Neurochir (Wien) 1991; 112 (1-2): 19-24
- 9 Lanzino G, Andreoli A, Tognetti F. et al. Orbital pain and unruptured carotid-posterior communicating artery aneurysms: the role of sensory fibers of the third cranial nerve. Acta Neurochir (Wien) 1993; 120 (1-2): 7-11
- 10 Birchall D, Khangure MS, McAuliffe W. Resolution of third nerve paresis after endovascular management of aneurysms of the posterior communicating artery. AJNR Am J Neuroradiol 1999; 20 (03) 411-413
- 11 Chalouhi N, Theofanis T, Jabbour P. et al. Endovascular treatment of posterior communicating artery aneurysms with oculomotor nerve palsy: clinical outcomes and predictors of nerve recovery. AJNR Am J Neuroradiol 2013; 34 (04) 828-832
- 12 Fujiwara S, Fujii K, Nishio S, Matsushima T, Fukui M. Oculomotor nerve palsy in patients with cerebral aneurysms. Neurosurg Rev 1989; 12 (02) 123-132
- 13 Leivo S, Hernesniemi J, Luukkonen M, Vapalahti M. Early surgery improves the cure of aneurysm-induced oculomotor palsy. Surg Neurol 1996; 45 (05) 430-434



