- 1Department of Neurosurgery, University of Helsinki and Helsinki University Hospital, Helsinki, Finland
- 2Department of Neurosurgery, Medical Faculty and University Hospital Düsseldorf, Heinrich-Heine-University Düsseldorf, Düsseldorf, Germany
- 3Department of Neurosurgery, King Edward Medical University, Lahore, Pakistan
Introduction: The aneurysms of the anterior inferior cerebellar artery (AICA) are rare lesions of the posterior circulation and to treat them is challenging. We aim to present anatomical and morphological characteristics of AICA aneurysms in a series of 15 patients.
Method: The DSA and CT angiography images of AICA aneurysms in 15 consecutive patients were analyzed retrospectively. Different anatomical characteristics were quantified, including morphology, location, width, neck width, length, bottleneck factor, and aspect ratio.
Results: Eighty percent of the patients were females. The age was 52.4 ± 9.6 (mean ± SD) years. 11 patients were smokers. Ten patients had a saccular aneurysm and five patients had a fusiform aneurysm. Aneurysm in 10 patients were located in the proximal segment, in three patients in the meatal segment, and in two patients in the distal segment. Ten out of 15 patients presented with a ruptured aneurysm. The size of AICA aneurysms was 14.8 ± 18.9 mm (mean ± SD). The aspect ratio was 0.92 ± 0.47 (mean ± SD) and bottleneck factor was 1.66 ± 1.65 (mean ± SD).
Conclusion: AICA aneurysms are rare lesions of posterior circulation predominantly found in females, present predominantly with subarachnoid hemorrhage, and are mostly large in size.
1. Introduction
The aneurysm of the anterior inferior cerebellar artery (AICA) are very rare and they account for <1% of all intracranial aneurysms (1, 2). The reported case reports of AICA aneurysms have a single or a few patients (1, 3–62), except for a few larger case series (63), including a large series of AICA aneurysms reported by Drake and colleagues (64). However, in this series, the aneurysms originating from the basilar trunk that is near the origin of AICA were included. AICA aneurysms are more often large in size, which makes their surgical and endovascular treatments challenging. Coiling is the favored treatment of posterior circulation aneurysms (65). However, in selected cases surgery might be a better choice, particularly in larger sized AICA aneurysms (26, 57). The surgical approach depends on location of aneurysm in relation to clivus. Aneurysms laying high can be approached through sub-temporal approach and low laying aneurysms are approached through retro-sigmoidal corridor. The morphological features may be helpful in deciding upon a treatment strategy. Due to the rarity of these lesions, the anatomical and radiological characteristics in unselected patient cohorts with AICA aneurysms have seldom been reported. In this series, we report the radiological features including shape, size, aspect ratio (maximum perpendicular height divided by neck diameter), bottleneck factor (maximum height to width ratio), and frequencies of aneurysm location in different segments of AICA aneurysms in a medium-size series. We report 15 consecutive patients harboring AICA aneurysms admitted from 1968 to 2017 in Helsinki University Hospital, department of Neurosurgery.
2. Methods
2.1. Patients and radiological data
Through retrospective analysis of our aneurysm data base, a total of 21 patients harbouring AICA aneurysms were identified. Six patients were excluded because of missing CT angiography scans or DSA. The remaining 15 patients harboring AICA aneurysms were included in the study. A 4-slice scanner (GE Lightspeed QX/I; GE Medical Systems, Milwaukee, Wisconsin, USA) was used for analyzing CT angiography images until 2007. Since then, a 32-slice scanner (GE LightSpeed Pro 32) or a 64-row scanner (GE lightSpeed VCT Advantage) was used to analyze CT angiography images. The digital archiving system of the hospital (IMPAX, version 5.3, Agfa, Mortsel, Belgium) was used to store the images. Two board-certified neurosurgeons analyzed the CTA scans.
The study was approved by the local ethical committee. The ethical number for the aneurysm database is HUS/197/2016. For retrospective data collection, an additional approval/consent was not required.
2.2. Radiological measurements
For each aneurysm, the maximal length, width, neck diameter, shape (saccular/fusiform), and the location at different segments of AICA were quantified. The above measurements were used to calculate aspect ratio and bottleneck factor.
2.3. Statistical analysis
The commercial statistical software IBM SPSS (version 20.0.0.) was used to analyze the data. The data is presented as mean ± SD or in frequencies (percentage).
3. Results
3.1. Patients and aneurysms
In our series (from 1968 to 2017), a total of 9,832 patients harboring intracranial aneurysms were studied. 21 patients out of 9,832 had AICA aneurysms showing an incidence of AICA aneurysms occurrence in about 0.22% of all intracranial aneurysms. Due to missing proper scans, we could analyze AICA aneurysms in 15 patients. Out of the 15 patients with AICA aneurysms, 12 (80%) were female and 3 (20%) were males. The mean age of the patients was 52.4 ± 9.6 years. In this case series, 11 (73%) of the patients were smokers. Also, 11 (73%) of the patients had a ruptured aneurysm (Table 1).
3.2. Radiological characters of AICA aneurysms
Ten (67%) patients had a saccular aneurysm and five (33%) patients had a fusiform aneurysm. Ten (67%) aneurysms were located in the pre-meatal segment, three (20%) aneurysms were located in the meatal segment, and the two (13%) aneurysms were located in the post-meatal segment. The AICA aneurysms had a mean size of 14.8 ± 18.9 mm. The ACIA aneurysm had a mean aspect ratio of 0.92 ± 0.47 and they had a mean bottleneck factor of 1.66 ± 1.65 (Table 2). Interestingly, in the proximal segment 30% and in the distal segments 40% of the aneurysms were fusiform (Tables 1, 2).
3.3. Clinical presentation and outcomes
Out of 15 patients, 11 (63.3%) presented with subarachnoid hemorrhage, and 4 (26.7%) patients with incidental findings. Among the ruptured cases 9 out of 11 (81.8%) presented with a good grade SAH (Hunt and Hess grade 1–3) and the remaining 2 out of 11 patients presented with a poor grade SAH (Hunt and Hess 4–5). In radiological analysis 3 out of 15 patients presented with intracerebral hematoma and 6 out of 15 patients presented with intraventricular hemorrhage as reported by Muhammad et al. in 2023. 11 out of 15 patients were treated surgically, only one patient was treated with endovascular coiling and 3 patients remain conservative. One of the conservatively treated patient lived more than 40 years and finally died in 2012 due to other systemic diseases and not due to SAH. In other two cases, patients were admitted with poor grade SAH and did not survive from severe SAH. All the unruptured aneurysms had good clinical outcomes (mRS 1–2) on discharge. In patients with ruptured AICA aneurysms, 9 out of 11 patients (81.8%) had good clinical outcomes (mRS 1–2) and 2 out of 11 patients (18.2%) had poor clinical (mRS 3–6) outcomes (66).
4. Discussion
AICA aneurysms are rare and have been reported in <1% of all intracranial aneurysms (1, 2). Our data show that the incidence of AICA aneurysms in an unselected cohort was 0.22%. The most common presentation of an AICA aneurysm is subarachnoid hemorrhage (SAH). Seventy three percent of patients in our series presented with SAH, which is similar to previously published data (63). A review of data from already published case reports of 56 patients revealed that 81% of patients presented with SAH, which is slightly greater than our series and the series presented previously. Patients with more insidious onset present with cranial nerve deficits very similar to cerebellopontine angle space occupying lesions. However, patients with SAH may also have cranial nerve deficits often in the seventh and eighth cranial nerves. In our series, 33% (N = 5) of the patients had cranial nerve (VI, VII, VIII, or IX) deficits (Table 1). Rarely, patients with an AICA aneurysm present with convulsive seizure (36). In our series, none of the patients presented with epilepsy. AICA can be anatomically divided into four segments including (67) anterior pontine (a1), lateral pontine (a2), flocculopeduncular (a3), and cortical (a4). The lateral pontine segment has a close relationship with the porus of the internal acoustic meatus and with the facial and cochleovestibular nerves. AICA aneurysms can be categorized into proximal, meatal, and distal (58). Our data shows that 67% (n = 10) of the aneurysms were located proximally, 20% (n = 3) were in the meatal region, and only 13% (n = 2) were located distally. Our data are consistent with a previously published short case series where five out of six aneurysms were located proximally (1). Meatal aneurysms can be further classified into three subtypes (58). Type I (also called remote) are localized in the vascular loop outside the meatus. Type II (plugged) aneurysms are partially buried in the internal-acoustic meatus, and type III (buried) are entirely contained by the internal auditory canal). In our series, we found three aneurysms that were located in the meatal segment. Two of these were type I and one was type II (not shown in the table). The location of the aneurysm facilitates the planning of a suitable surgical approach if surgery is indicated (Figures 1–3). Most of the AICA aneurysms are reached through retrosigmoid approach (Figures 1–3). The mean ± SD size of the AICA aneurysms was 14.8 ± 18.9. The mean ± SD width was 16.9 ± 20.3 mm and the mean ± SD length was 16.9 ± 20.3 (Table 2). It is noteworthy that 73% of the patients were smokers and smoking is a potential risk factor for aneurysm formation and rupture. Further analysis of saccular aneurysms (n = 10) revealed a mean ± SD aspect ratio of 0.92 ± 0.47 and a mean ± SD bottleneck factor of 1.66 ± 1.65 (Table 2). Our data demonstrate that most AICA aneurysms are larger in size, which is consistent with a previous report that analyzed 10 thrombosed AICA aneurysms (20). In most cases in this series, the aneurysm size was >10 mm; two of these aneurysms were giant.
Figure 1. Demonstration of a ruptured AICA aneurysms at proximal location (A,B) that was treated surgically through retrosigmoid approach (C). Another patients with ruptured high laying AICA aneurysm (D,E) that was treated through sub-temporal approach (F).
Figure 2. Demonstration of a ruptured AICA aneurysms with intra cerebral hemorrhage (A–C) that was treated through retrosigmoid approach (D–F).
Figure 3. Demonstration of a ruptured AICA aneurysms at meatal loop with intra cerebral hemorrhage (A–C) that was treated through retrosigmoid approach (D–F).
5. Conclusion
AICA aneurysms are rare posterior circulation lesions predominantly found in females, present predominantly with subarachnoid hemorrhage, are mostly large in size.
6. Limitations
Our analysis was retrospective and may not completely reflect the natural history of anatomical and radiological parameters. The aspect ratio was quantified in a few cases after rupture and hence the possibility remains that the aspect ratio might have changed due to morphological changes after rupture and to a compression effect due to subarachnoid blood. Due to the small number of patients, we could not analyze the influence of aspect ratio, bottleneck factor, and segmental location of the aneurysm on aneurysm rupture.
Data availability statement
The original contributions presented in the study are included in the article, further inquiries can be directed to the corresponding author.
Ethics statement
The studies involving human participants were reviewed and approved by the local ethical committee that approved the study of intracranial aneurysms. The ethical number for the aneurysm database is HUS/197/2016. An additional approval/consent for retrospective data collection was not required. Written informed consent for participation was not required for this study in accordance with the national legislation and the institutional requirements.
Author contributions
SM and MN contributed to the conception and design of the study. SM performed the statistical analysis. SM wrote the first draft of the manuscript. AH, HK, BJ, and RK, DH, MN wrote sections of the manuscript. All authors contributed to the article and approved the submitted version.
Funding
SM was supported by Ehrnrooth foundation for clinical vascular and skull base fellowship.
Conflict of interest
The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.
The author(s) SM and BJ declared that they were an editorial board member of Frontiers, at the time of submission. This had no impact on the peer review process and the final decision.
Publisher's note
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References
1. Li X, Zhang D, Zhao J. Anterior inferior cerebellar artery aneurysms: six cases and a review of the literature. Neurosurg Rev. (2012) 35(1):111–9; discussion 9. doi: 10.1007/s10143-011-0338-1
2. Sanai N, Tarapore P, Lee AC, Lawton MT. The current role of microsurgery for posterior circulation aneurysms: a selective approach in the endovascular era. Neurosurgery. (2008) 62(6):1236–49. ; discussion 49–53.18824990
3. Adorno JO, de Andrade GC. Aneurysm of the anterior inferior cerebellar artery: case report. Arq Neuropsiquiatr. (2002) 60(4):1019–24. doi: 10.1590/S0004-282X2002000600026
4. Aguiar GB, Veiga JC, Jory M, Souza RB, Mattar Neto B, Conti ML. Fusiforme aneurysm of the anterior inferior cerebellar artery and arteriovenous malformation fed by the same vessel. Medicina (B Aires). (2012) 72(3):245.22763162
5. Akyuz M, Tuncer R. Multiple anterior inferior cerebellar artery aneurysms associated with an arteriovenous malformation: case report. Surg Neurol. (2005) 64(Suppl 2):S106–8. doi: 10.1016/j.surneu.2005.07.037
6. Andrade G, Faquini I, Azevedo-Filho H, Laercio J, Camara D, Mendes JC, et al. Dissecting anterior inferior cerebellar artery aneurysm treated by endovascular route: report of three cases and review. Arq Neuropsiquiatr. (2010) 68(4):645–7. doi: 10.1590/S0004-282X2010000400031
7. Baskaya MK, Coscarella E, Jea A, Morcos JJ. Aneurysm of the anterior inferior cerebellar artery-posterior inferior cerebellar artery variant: case report with anatomical description in the cadaver. Neurosurgery. (2006) 58(2):E388; discussion E. doi: 10.1227/01.NEU.0000199344.63306.DD
8. Cantore GP, Ciappetta P, Vagnozzi R, Bozzao L. Giant aneurysm of the anterior inferior cerebellar artery simulating a cerebellopontine angle tumor. Surg Neurol. (1982) 18(1):76–8. doi: 10.1016/0090-3019(82)90025-8
9. DiMaio S, Mohr G, Dufour JJ, Albrecht S. Distal mycotic aneurysm of the AICA mimicking intracanalicular acoustic neuroma. Can J Neurol Sci. (2003) 30(4):388–92. doi: 10.1017/S0317167100003139
10. Ebara M, Tanaka T, Sawauchi S, Morooka S, Yuhki K, Abe T. A ruptured aneurysm of the anterior and posterior inferior cerebellar artery: a case report. No Shinkei Geka. (1999) 27(11):1013–7.10565045
11. Fukuya T, Kishikawa T, Ikeda J, Kudo S, Kuwano H, Matsumoto S, et al. Aneurysms of the peripheral portion of the anterior inferior cerebellar artery; report of two cases. Neuroradiology. (1987) 29(5):493–6. doi: 10.1007/BF00341751
12. Gleeson MJ, Cox TC, Strong AJ. Aneurysm of the anterior inferior cerebellar artery mimicking an intracanalicular acoustic neuroma. J Laryngol Otol. (1989) 103(1):107–10. doi: 10.1017/S0022215100108163
13. Gopalakrishnan CV, Menon G, Nair S. Aneurysm of the anterior inferior cerebellar artery-posterior inferior cerebellar artery variant: two case reports and review of literature. Br J Neurosurg. (2009) 23(5):554–6. doi: 10.1080/02688690902987778
14. Goto S, Ohshima T, Yamamoto T, Nishihori M, Nishizawa T, Shimato S, et al. A case of ruptured intrameatal aneurysm successfully treated with coil embolization. Nagoya J Med Sci. (2015) 77(1–2):307–13.25797996
15. Honda Y, Tanaka R, Kameyama S. Ruptured distal anterior inferior cerebellar artery aneurysm–case report. Neurol Med Chir (Tokyo). (1994) 34(11):763–7. doi: 10.2176/nmc.34.763
16. Ishii D, Takechi A, Shinagawa K, Sogabe T. Endovascular treatment for ruptured distal anterior inferior cerebellar artery aneurysm -case report. Neurol Med Chir (Tokyo). (2010) 50(5):396–9. doi: 10.2176/nmc.50.396
17. Ito J, Takeda N, Suzuki Y, Takeuchi S, Osugi S, Yoshida Y. The anterior inferior cerebellar arteries originating from the internal carotid artery (author’s transl). No to Shinkei. (1979) 31(10):999–104.508439
18. Jinbo Y, Zheng Z, Jiaquan H, Hui Y, Jun L. Embolization of a ruptured aneurysm of the distal anterior inferior cerebellar artery with parent artery preservation. Neurol India. (2010) 58(5):786–8. doi: 10.4103/0028-3886.72170
19. Johnson JH Jr, Kline DG. Anterior inferior cerebellar artery aneurysms. Case report. J Neurosurg. (1978) 48(3):455–60. doi: 10.3171/jns.1978.48.3.0455
20. Kanamori F, Kawabata T, Muraoka S, Kojima T, Watanabe T, Hatano N, et al. Ruptured partially thrombosed anterior inferior cerebellar artery aneurysms: two case reports and review of literature. Nagoya J Med Sci. (2016) 78(4):517–22.28008208
21. Kang HS, Roh HG, Han MH, Koh YC. Successful endovascular occlusion of a ruptured distal anterior inferior cerebellar artery aneurysm of the caudal trunk: case report. Interv Neuroradiol. (2007) 13(3):271–6.20566118
22. Kiya K, Uozumi T, Emoto K, Matsuoka T. Anterior inferior cerebellar artery aneurysm at the internal auditory meatus—case report. Neurol Med Chir (Tokyo). (1989) 29(7):592–5. doi: 10.2176/nmc.29.592
23. Kiya K, Uozumi T, Emoto K, Matsuoka T. Aneurysm of the anterior inferior cerebellar artery at the internal auditory meatus: case report and review of the literature. Hiroshima J Med Sci. (1989) 38(1):39–44.2666361
24. Koizumi H, Kurata A, Suzuki S, Miyasaka Y, Tanaka C, Fujii K. Endosaccular embolization for a ruptured distal anterior inferior cerebellar artery aneurysm. Radiol Case Rep. (2012) 7(2):651. doi: 10.2484/rcr.v7i2.651
25. Kyoshima K, Matsuda M, Handa J. Cerebral aneurysm of the distal anterior inferior cerebellar artery: case report. Nihon Geka Hokan. (1995) 64(6):139–45.8913090
26. Lee BS, Witek AM, Moore NZ, Bain MD. Treatment of an anterior inferior cerebellar artery aneurysm with microsurgical trapping and in situ posterior inferior cerebellar artery to anterior inferior cerebellar artery bypass: case report. Oper Neurosurg (Hagerstown). (2018) 15(4):418–24. doi: 10.1093/ons/opx275
27. Lee SJ, Koh JS, Ryu CW, Lee SH. Ruptured intrameatal aneurysm of the anterior inferior cerebellar artery accompanying an arteriovenous malformation: a case report. Cerebellum. (2012) 11(3):808–12. doi: 10.1007/s12311-011-0349-z
28. Lv X, Li Y, Liu A, Zhang J, Wu Z. Parent artery occlusion for peripheral anterior inferior cerebellar artery aneurysm. A case report and review of the literature. Neuroradiol J. (2008) 21(2):261–5. doi: 10.1177/197140090802100219
29. Mahmoud M, El Serwi A, Alaa Habib M, Abou Gamrah S. Endovascular treatment of AICA flow dependent aneurysms. A report of three cases and review of the literature. Interv Neuroradiol. (2012) 18(4):449–57.23217640
30. Marchini AK, Mosimann PJ, Guichard JP, Boukobza M, Houdart E. Anterior inferior cerebellar artery aneurysms mimicking vestibular schwannomas. J Neuroimaging. (2014) 24(4):404–6. doi: 10.1111/j.1552-6569.2012.00752.x
31. Martin RG, Grant JL, Peace D, Theiss C, Rhoton AL Jr. Microsurgical relationships of the anterior inferior cerebellar artery and the facial-vestibulocochlear nerve complex. Neurosurgery. (1980) 6(5):483–507. doi: 10.1227/00006123-198005000-00001
32. Mascitelli JR, McNeill IT, Mocco J, Berenstein A, DeMattia J, Fifi JT. Ruptured distal AICA pseudoaneurysm presenting years after vestibular schwannoma resection and radiation. J Neurointerv Surg. (2016) 8(5):e19. doi: 10.1136/neurintsurg-2015-011736.rep
33. Matsushige T, Ikawa F, Ohbyashi N, Imada Y, Kajiwara Y, Inagawa T. Ruptured aneurysm arising from the anterior medullary segment of the posterior inferior cerebellar artery: report of two cases. No Shinkei Geka. (2004) 32(8):867–74.15478654
34. Matsuyama T, Okuchi K, Norimoto K, Ueyama T. Ruptured dissecting anterior inferior cerebellar artery aneurysm–case report. Neurol Med Chir (Tokyo). (2002) 42(5):214–6. doi: 10.2176/nmc.42.214
35. Menovsky T, Andre Grotenhuis J, Bartels RH. Aneurysm of the anterior inferior cerebellar artery (AICA) associated with high-flow lesion: report of two cases and review of literature. J Clin Neurosci. (2002) 9(2):207–11.11922719
36. Mizushima H, Kobayashi N, Yoshiharu S, Kazuo H, Dohi K, Sasaki K, et al. Aneurysm of the distal anterior inferior cerebellar artery at the medial branch: a case report and review of the literature. Surg Neurol. (1999) 52(2):137–42. doi: 10.1016/S0090-3019(99)00042-7
37. Mori K, Miyazaki H, Ono H. Aneurysm of the anterior inferior cerebellar artery at the internal auditory meatus. Surg Neurol. (1978) 10(5):297–300.725737
38. Nakagawa K, Sakaki S, Kimura H, Matsuoka K. Aneurysm of the anterior inferior cerebellar artery at the internal auditory meatus. Surg Neurol. (1984) 21(3):231–5. doi: 10.1016/0090-3019(84)90192-7
39. Nishimoto A, Fujimoto S, Tsuchimoto S, Matsumoto Y, Tabuchi K, Higashi T. Anterior inferior cerebellar artery aneurysm. Report of three cases. J Neurosurg. (1983) 59(4):697–702. doi: 10.3171/jns.1983.59.4.0697
40. Oh JS, Yoon SM. Endovascular treatment for ruptured distal anterior inferior cerebellar artery aneurysm. (2014) 16(1):20–5.24765609
41. Okumura Y, Sakaki T, Hirabayashi H, Shimomura T. Intrameatal aneurysm successfully treated by meatal loop trapping–case report. Neurol Med Chir (Tokyo). (1999) 39(2):161–4. doi: 10.2176/nmc.39.161
42. Pasler D, Baldauf J, Runge U, Schroeder HW. Intrameatal thrombosed anterior inferior cerebellar artery aneurysm mimicking a vestibular schwannoma. J Neurosurg. (2011) 114(4):1057–60. doi: 10.3171/2010.9.JNS10491
43. Pritz MB. Aneurysms of the anterior inferior cerebellar artery. Acta Neurochir. (1993) 120(1–2):12–9. doi: 10.1007/BF02001463
44. Russegger L, Furtschegger A. Aneurysms of the anterior inferior cerebellar artery. A case report and review of the literature. Nervenarzt. (1990) 61(8):499–503.2234227
45. Saito R, Tominaga T, Ezura M, Shimizu H, Yoshimoto T. Distal anterior inferior cerebellar artery aneurysms: report of three cases and literature review. No Shinkei Geka. (2001) 29(8):709–14.11554088
46. Santillan A, Gobin YP, Patsalides A, Riina HA, Rosengart A, Stieg PE. Endovascular management of distal anterior inferior cerebellar artery aneurysms: report of two cases and review of the literature. Surg Neurol Int. (2011) 2:95. doi: 10.4103/2152-7806.82577
47. Santucci N, Gazzeri G, Magliocco C. Aneurysm of the anterior inferior cerebellar artery (AICA). 18th case in the literature. Riv Neurol. (1985) 55(1):30–7.4023549
48. Sarkar A, Link MJ. Distal anterior inferior cerebellar artery aneurysm masquerading as a cerebellopontine angle tumor: case report and review of literature. Skull Base. (2004) 14(2):101–6. ; discussion 6–7.16145591
49. Sasame J, Nomura M. Dissecting aneurysm of anterior inferior cerebellar artery initially presenting with nonhemorrhagic symptom. J Stroke Cerebrovasc Dis. (2015) 24(8):e197–9. doi: 10.1016/j.jstrokecerebrovasdis.2015.03.055
50. Singh S, Mittal RS, Purohit D, Shekhawat J. Spontaneous resolution of ruptured dissecting anterior inferior cerebellar artery aneurysm: a rare case report. Asian J Neurosurg. (2017) 12(3):570–2. doi: 10.4103/1793-5482.145561
51. Spallone A, De Santis S, Giuffre R. Peripheral aneurysms of the anterior inferior cerebellar artery. Case report and review of literature. Br J Neurosurg. (1995) 9(4):537–41. doi: 10.1080/02688699550041197
52. Suh SH, Kim DJ, Kim DI, Kim BM, Chung TS, Hong CK, et al. Management of anterior inferior cerebellar artery aneurysms: endovascular treatment and clinical outcome. AJNR Am J Neuroradiol. (2011) 32(1):159–64. doi: 10.3174/ajnr.A2360
53. Sun Y, Wrede KH, Chen Z, Bao Y, Ling F. Ruptured intrameatal AICA aneurysms—a report of two cases and review of the literature. Acta Neurochir. (2009) 151(11):1525–30. doi: 10.1007/s00701-009-0269-6
54. Suzuki K, Meguro K, Wada M, Fujita K, Nose T. Embolization of a ruptured aneurysm of the distal anterior inferior cerebellar artery: case report and review of the literature. Surg Neurol. (1999) 51(5):509–12. doi: 10.1016/S0090-3019(97)00462-X
55. Takeuchi S, Takasato Y, Masaoka H, Hayakawa T, Otani N, Yoshino Y, et al. Trapping of ruptured dissecting aneurysm of distal anterior inferior cerebellar artery—case report. Brain Nerve. (2009) 61(2):203–7.19235471
56. Tamura Y, Shirai W, Tokumitsu N. Intrameatal aneurysm of distal anterior inferior cerebellar artery manifesting a subarachnoid hemorrhage: a report of 2 cases. No Shinkei Geka. (2018) 46(8):673–81.
57. Taussky P, Garber S, Schmidt RH. Surgical management of a ruptured and unruptured distal anterior inferior cerebellar artery aneurysm. Report of 2 cases and review of the literature. Cent Eur Neurosurg. (2011) 72(2):108–11. doi: 10.1055/s-0030-1268498
58. Yamakawa H, Hattori T, Tanigawara T, Sahashi Y, Ohkuma A. Intracanalicular aneurysm at the meatal loop of the distal anterior inferior cerebellar artery: a case report and review of the literature. Surg Neurol. (2004) 61(1):82–8; discussion 8. doi: 10.1016/S0090-3019(03)00270-2
59. Yokoyama S, Kadota K, Asakura T, Kawazoe K. Aneurysm of the distal anterior inferior cerebellar artery—case report. Neurol Med Chir (Tokyo). (1995) 35(8):587–90. doi: 10.2176/nmc.35.587
60. Zager EL. Isolated trigeminal sensory loss secondary to a distal anterior inferior cerebellar artery aneurysm: case report. Neurosurgery. (1991) 28(2):288–91. doi: 10.1227/00006123-199102000-00018
61. Zlotnik EI, Sklyut JA, Smejanovich AF, Stasenko EN. Saccular aneurysm of the anterior inferior cerebellar-internal auditory artery. Case report. J Neurosurg. (1982) 57(6):829–32. doi: 10.3171/jns.1982.57.6.0829
62. Zotta DC, Stati G, De Paulis D, Galzio RJ. Intrameatal aneurysm of the anterior inferior cerebellar artery. J Clin Neurosci. (2011) 18(4):561–3.21257312
63. Gonzalez LF, Alexander MJ, McDougall CG, Spetzler RF. Anteroinferior cerebellar artery aneurysms: surgical approaches and outcomes—a review of 34 cases. Neurosurgery. (2004) 55(5):1025–35. doi: 10.1227/01.NEU.0000141083.00866.82
64. Bojanowski MW BI, Robert T. Anterior inferior cerebellar artery aneurysms. In: Rangel-Castilla LNP, Siddiqui AH, Spetzler RF, Levy EI, editors. Decision making in neurovascular disease. Thieme (2018).
65. Spetzler RF, McDougall CG, Zabramski JM, Albuquerque FC, Hills NK, Russin JJ, et al. The barrow ruptured aneurysm trial: 6-year results. J Neurosurg. (2015) 123(3):609–17. doi: 10.3171/2014.9.JNS141749
66. Muhammad S, Hafez A, Kaukovalta H, Jahromi BR, Kivisaari R, Hanggi D, et al. Treatment and outcome of anterior inferior cerebellar artery (AICA) aneurysms: helsinki series of 15 consecutive patients. Asian J Neurosurg. (2023) 18(1):30–5. doi: 10.1055/s-0042-1758844
Keywords: AICA aneurysms, characteristics of AICA aneurysms, CT angiography, radiological features, clinical outcome
Citation: Muhammad S, Hafez A, Kaukovalta H, Rezai Jahromi B, Kivisaari R, Hänggi D and Niemelä M (2023) Anterior inferior cerebellar artery (AICA) aneurysms: a radiological study of 15 consecutive patients. Front. Radiol. 3:1229921. doi: 10.3389/fradi.2023.1229921
Received: 27 May 2023; Accepted: 18 July 2023;
Published: 8 August 2023.
Edited by:
David Pelz, Western University, CanadaReviewed by:
Bharat Hosur, Armed Forces Medical College, IndiaGennaro D’Anna, ASST Ovest Milanese, Italy
© 2023 Muhammad, Hafez, Kaukovalta, Rezai Jahromi, Kivisaari, Hänggi and Niemelä. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
*Correspondence: Sajjad Muhammad c2FqamFkLm11aGFtbWFkQG1lZC51bmktZHVlc3NlbGRvcmYuZGU=