CC BY-NC-ND 4.0 · Asian J Neurosurg 2023; 18(01): 201-205
DOI: 10.1055/s-0043-1764119
Case Report

Fenestrated Anterior Communicating Artery Complex Mimicking an Unruptured Aneurysm: Diagnostic Pitfall

Atsushi Tsukada
1   Department of Neurosurgery, Tsukuba Memorial Hospital, Kaname, Tsukuba, Ibaraki, Japan
,
Kiyoyuki Yanaka
1   Department of Neurosurgery, Tsukuba Memorial Hospital, Kaname, Tsukuba, Ibaraki, Japan
,
Hayato Takeda
1   Department of Neurosurgery, Tsukuba Memorial Hospital, Kaname, Tsukuba, Ibaraki, Japan
,
Kuniyuki Onuma
1   Department of Neurosurgery, Tsukuba Memorial Hospital, Kaname, Tsukuba, Ibaraki, Japan
,
Maya Takada
1   Department of Neurosurgery, Tsukuba Memorial Hospital, Kaname, Tsukuba, Ibaraki, Japan
,
Kazuhiro Nakamura
1   Department of Neurosurgery, Tsukuba Memorial Hospital, Kaname, Tsukuba, Ibaraki, Japan
,
Eiichi Ishikawa
2   Department of Neurosurgery, Faculty of Medicine, University of Tsukuba, Tennodai 1-1-1, Tsukuba, Ibaraki, Japan
› Institutsangaben
 

Abstract

Anatomical variations often occur in the anterior communicating artery (AComA) complex, and a careful preoperative evaluation is required before repair of this lesion. We report a case of a fenestrated AComA complex mimicking an unruptured cerebral aneurysm. A 49-year-old woman was referred to our hospital under suspicion of unruptured aneurysms of the AComA and the left middle cerebral artery on magnetic resonance angiography (MRA). Additional three-dimensional computed tomographic angiography (CTA) showed the lesion arising from the AComA complex with a maximum diameter of 4.2 mm. Intraoperative findings showed that the putative aneurysm was actually a fenestrated AComA complex as the blood vessels that formed the AComA complex were dilated and meandering. After the operation, MRA and CTA three-dimensional images were reviewed again but we could still not diagnose the lesion as a fenestrated AComA complex rather than an aneurysm. However, in the MRA source image, a secant line in the lesion was the only finding suggestive of a fenestration. The AComA complex is often associated with various vascular malformations, and it is essential to consider this association in the preoperative evaluation. The interpretation of source images may be helpful for accurate diagnosis and surgical planning.


#

Introduction

With recent advances in non-invasive diagnostic imaging methods, such as magnetic resonance (MR) imaging and computed tomography (CT), the detection rate of unruptured cerebral aneurysms is increasing. Imaging techniques for visualizing intracranial vasculature include MR angiography (MRA), CT angiography (CTA), and digital subtraction angiography (DSA). DSA is a gold standard but invasive and noninvasive MRA and/or CTA are often used instead of DSA to delineate and monitor the aneurysm.[1] [2]

According to a recent survey of cerebrovascular treatment specialists, for aneurysms in locations other than the MCA, 68% of unruptured aneurysms and 73% of ruptured aneurysms underwent microsurgery without preoperative DSA.[3] Therefore, when planning treatment for aneurysms without DSA, it is necessary to be familiar with the diagnostic pitfalls of MRI and CTA.

The AComA complex is a challenging part of the preoperative vascular evaluation as vascular malformations, including fenestration, are often encountered during AComA aneurysm surgery.[4] Here, we report a case of a fenestrated AComA complex that was inaccurately diagnosed by CTA and several MRAs before surgery.


#

Case Description

A 49-year-old woman was referred to our hospital under suspicion of unruptured cerebral aneurysms of the AComA and the left middle cerebral artery. MRI was performed using a 1.5T MRI scanner (Philips, Philips Achieva, Amsterdam, Netherlands) for a checkup 5 years ago at our hospital that showed no abnormalities. The imaging conditions were repetition time (TR); 24 ms, echo time (TE); 6.91 ms, flip angle (FA); 17, and the thickness was 1.7 mm ([Fig. 1A]).

Zoom Image
Fig. 1 Magnetic resonance (MR) angiography (upper) and its source image (lower) were taken at the age of 44 (A), 49 (B), and 51 (C) years. The 1.5 Tesla MR angiography showing no obvious aneurysm (A). The 3.0 Tesla MR angiography showing an aneurysm (arrow) arising from the anterior communicating artery complex (B, C). The initial MR angiographs point to an aneurysm arising from the complex of the anterior communicating artery (B, C).

Although the possibility of de novo aneurysms could not be ruled out, the patient was conservatively followed up with a 3.0 Tesla MRI every 6 months (Philips, Philips Ingenia Cx, Amsterdam, Netherlands or Philips, Amsterdam, the Netherlands). The imaging conditions were TR; 24 ms, TE; 6.91 ms, FA; 17, and the thickness; 1.3 mm) ([Fig. 1B,C]).

MRI at the age of 51 years showed a gradual growth in the AComA aneurysm ([Fig. 1B,C]), while an additional three-dimensional CTA (3D-CTA) showed an aneurysm arising from the right A1-A2 junction with a maximum diameter of 4.2 mm ([Fig. 2]). The 3D-CTA was performed with iopamidol 370 on a multi-detector CT scanner (Philips, IQon spectral CT, Amsterdam, the Netherlands) with 64 detector rows. The protocol consisted of 64 × 0.625 mm collimation, 1 mm slide, 0.703 pitch, and 120 kV tube voltage).The size of the aneurysm was still small, less than 5 mm, but demonstrated gradual growth.

Zoom Image
Fig. 2 The three-dimensional computed tomography (CT) angiography (A; lateral view, B; A-P view) showing suspected aneurysm (arrow) arising from the right A1-A2 junction. The source image of the CT angiography also showing the lesion arising from the anterior communicating artery complex.

Considering the risk of rupture, a right pterional craniotomy was performed to obliterate the AComA aneurysm. No aneurysm was observed in the expected area, and the lesion, which was preoperatively diagnosed as an aneurysm, was actually a fenestrated AComA complex as the blood vessels forming the AComA complex were dilated and meandering. A small aneurysm-like bulge with strong arteriosclerosis was found in the ipsilateral right A2-fenestrated AComA junction ([Fig. 3]) and coated with a piece of muscle and fibrin glue. The postoperative course was uneventful and the patient was discharged 8 days after surgery. Such unruptured/untreated left middle cerebral artery aneurysms are followed up regularly with MRI.

Zoom Image
Fig. 3 Intraoperative images showing fenestrated anterior communicating artery (AComA) complex with no obvious aneurysm (dotted line: fenestrated AComA, arrow: right A1 segment, arrowhead: left A1 segment, double arrowhead: left A2 segment, white asterisk: fenestration). The magnified view (right) with the vessels forming the fenestration showing dilatation and meandering with pronounced atherosclerosis. The right A2 segment (double arrow) and a small aneurysm-like bulge (black asterisk) with strong arteriosclerosis in the right A2- fenestrated AComA junction were also found.

#

Discussion

Intracranial arterial fenestration is an anatomic variant more often manifesting at the AComA complex and basilar artery junction.[5] AComA forms part of the circle of Willis and is developed by the fusion of the medial vascular network between the left and right anterior cerebral arteries, which is itself derived from the cranial division of the primitive internal carotid artery,[6] and several variations have been reported.[7] In both endovascular treatment and microsurgical clipping, preoperative evaluation, including the spatial relationship with the blood vessels around the aneurysm (in addition to the size and the shape of the aneurysm itself), is imperative.[7] [8] [9] [10] However, such complex vasculature renders accurate diagnosis difficult.

Due to recent advances in imaging technology, the diagnostic accuracy of noninvasive MRI plus 3D-CTA is ever increasing. A recent systematic review and meta-analysis of MRA in the detection of intracranial aneurysms reported sensitivity and specificity of 95% and 89%, respectively, when compared to DSA.[11] Similar studies have been conducted with CTA and found a sensitivity and specificity of 90% or more.[12] [13] [14] Recently, MRA at 3.0 Tesla has a good correlation with DSA and aneurysms as small as 1 mm in size can be detected.[15] [16]

According to the latest research, about 70% of cases undergo microsurgery without preoperative DSA.[3] Therefore, when planning the treatment of an aneurysm without DSA, it is essential to be familiar with the diagnostic pitfalls of MRI and CTA. As a pitfall of MRI, we assume that the aneurysm-like lesion appeared larger because of the change from 1.5 T to 3.0 T and/or because of the different slice thickness, and probably not because of the small AN-like bulge seen in the operative field. We should note that lesions are seen differently when we change MRI models or imaging conditions.

The usual preoperative evaluation of unruptured cerebral aneurysms is performed solely by MRA plus 3D-CTA in our hospital. DSA is added in cases to clarify features or where endovascular treatment seems to be more suitable than craniotomy. However, noninvasive imaging methods may result in false-positive or false-negative findings for aneurysms with a diameter of 3 mm or less, anomalies located near bony structures, or lesions of the AComA complex, internal carotid artery, or posterior circulatory system.[17] [18] [19] [20] In our case, DSA was not performed because the aneurysm was identified on both MRA and CTA and the size of the aneurysm was over 3 mm in diameter. The 3D images of MRA and CTA were carefully reviewed again after surgery, but the lesion could not be diagnosed as a fenestrated AComA complex rather than an aneurysm.

DSA remains the gold standard for imaging quality and detection sensitivity in the evaluation of intracranial vessels.[21] If DSA or 3D rotational catheter angiography had been performed preoperatively, the correct diagnosis could have been obtained in our case. However, there are reports of cases in which DSA or 3D rotational angiography mistook a vascular abnormality of the AComA complex for an aneurysm.[22] [23] Therefore, it should be recognized that even DSA does not have 100% diagnostic ability. In particular, DSA has difficulty assessing aneurysm thrombosis and calcification around the aneurysm neck. Consequently, physicians need to understand the strengths and weaknesses of each imaging method when choosing an imaging modality.

Interestingly, careful, retrospective observation of this case's source MRA images revealed a secant line in the lesion ([Fig. 4]), suggestive of fenestration. Therefore, a detailed interpretation of the source images from MRA and CTA, as well as 3D images, may be helpful for accurate diagnosis in some cases. Because the AComA complex itself has diverse phenotypes and can be difficult to diagnose, the use of multiple diagnostic methods, including DSA, can be definitely recommended. Our case thus draws further attention to the preoperative diagnostic modalities used for this region.

Zoom Image
Fig. 4 Review of original MR angiography images taken at the age of 51 years with a suspected secant line in an aneurysm-like lesion (arrow).

#

Conclusion

The AComA complex is often associated with various vascular malformations and it is essential to consider this association in the preoperative evaluation. The interpretation of source images may be helpful for accurate diagnosis and surgical planning.


#
#

Conflict of Interest

None declared.

Acknowledgments

We thank Dr. Alexander Zaboronok, MD, PhD, Assistant Professor, Department of Neurosurgery, Faculty of Medicine of the University of Tsukuba for professional and English revision, and Dr. Bryan J. Mathis of the University of Tsukuba Hospital International Medical Center for language revision.

Authors' Contributions

Substantial contributions to the conception or design of the work; or the acquisition, analysis, or interpretation of data for the work: Atsushi Tsukada and Kiyoyuki Yanaka. Drafting the work: Atsushi Tsukada. Revising it critically for important intellectual content: Kiyoyuki Yanaka, Hayato Takeda, Kuniyuki Onuma, Maya Takada, Kazuhiro Nakamura, and Eiichi Ishikawa. Final approval of the version to be published: Eiichi Ishikawa and all other coauthors. Agreement to be accountable for all aspects of the work in ensuring that questions related to the accuracy or integrity of any part of the work are appropriately investigated and resolved: Eiichi Ishikawa.


  • References

  • 1 Howard BM, Hu R, Barrow JW, Barrow DL. Comprehensive review of imaging of intracranial aneurysms and angiographically negative subarachnoid hemorrhage. Neurosurg Focus 2019; 47 (06) E20
  • 2 Tsunou K, Yamanaka R. Usefulness of the low tube voltage scan in the head CT-angiography with the subarachnoid hemorrhage. Journal of Japanese Society for Emergency Medicine. 2018; 21: 672-679
  • 3 Choi JH, Jo KII, Kim KH. et al. Morphological risk factors for the rupture of anterior communicating artery aneurysms: the significance of fenestration. Neuroradiology 2016; 58 (02) 155-160
  • 4 Cooke DL, Stout CE, Kim WT. et al. Cerebral arterial fenestrations. Interv Neuroradiol 2014; 20 (03) 261-274
  • 5 Osborn AG. Diagnostic Cerebral Angiography. 2nd ed. Philadelphia: Lippincott Williams & Wilkins; 1999: 105-116
  • 6 López-Sala P, Alberdi N, Mendigaña M, Bacaicoa MC, Cabada T. Anatomical variants of anterior communicating artery complex. A study by computerized tomographic angiography. J Clin Neurosci 2020; 80: 182-187
  • 7 Kwak R, Niizuma H, Hatanaka M, Suzuki J. Anterior communicating artery aneurysms accompanied with anomalies or anterior communicating artery (author's transl) [article in Japnese]. No To Shinkei 1978; 30 (11) 1221-1225
  • 8 Kwak R, Niizuma H, Hatanaka M, Suzuki J. Anterior communicating artery aneurysms with associated anomalies. J Neurosurg 1980; 52 (02) 162-164
  • 9 Cai W, Hu C, Gong J, Lan Q. Anterior communicating artery aneurysm morphology and the risk of rupture. World Neurosurg 2018; 109: 119-126
  • 10 Sailer AM, Wagemans BA, Nelemans PJ, de Graaf R, van Zwam WH. Diagnosing intracranial aneurysms with MR angiography: systematic review and meta-analysis. Stroke 2014; 45 (01) 119-126
  • 11 Chappell ET, Moure FC, Good MC. Comparison of computed tomographic angiography with digital subtraction angiography in the diagnosis of cerebral aneurysms: a meta-analysis. Neurosurgery 2003; 52 (03) 624-631 , discussion 630–631
  • 12 Menke J, Larsen J, Kallenberg K. Diagnosing cerebral aneurysms by computed tomographic angiography: meta-analysis. Ann Neurol 2011; 69 (04) 646-654
  • 13 White PM, Wardlaw JM, Easton V. Can noninvasive imaging accurately depict intracranial aneurysms? A systematic review. Radiology 2000; 217 (02) 361-370
  • 14 Bernstein MA, Huston III J, Lin C, Gibbs GF, Felmlee JP. High-resolution intracranial and cervical MRA at 3.0T: technical considerations and initial experience. Magn Reson Med 2001; 46 (05) 955-962
  • 15 Tang PH, Hui F, Sitoh YY. Intracranial aneurysm detection with 3T magnetic resonance angiography. Ann Acad Med Singap 2007; 36 (06) 388-393
  • 16 Serizawa T, Saeki N, Yamaura A. Microsurgical anatomy and clinical significance of the anterior communicating artery and its perforating branches. Neurosurgery 1997; 40 (06) 1211-1216 , discussion 1216–1218
  • 17 Sebök M, Dufour JP, Cenzato M. et al. When is diagnostic subtraction angiography indicated before clipping of unruptured and ruptured intracranial aneurysms? An international survey of current practice. Acta Neurochir Suppl (Wien) 2021; 132: 9-17
  • 18 Turan N, Heider RA, Roy AK. et al. Current perspectives in imaging modalities for the assessment of unruptured intracranial aneurysms: a comparative analysis and review. World Neurosurg 2018; 113: 280-292
  • 19 Okahara M, Kiyosue H, Yamashita M. et al. Diagnostic accuracy of magnetic resonance angiography for cerebral aneurysms in correlation with 3D-digital subtraction angiographic images: a study of 133 aneurysms. Stroke 2002; 33 (07) 1803-1808
  • 20 Pradilla G, Wicks RT, Hadelsberg U. et al. Accuracy of computed tomography angiography in the diagnosis of intracranial aneurysms. World Neurosurg 2013; 80 (06) 845-852
  • 21 Korogi Y, Takahashi M, Katada K. et al. Intracranial aneurysms: detection with three-dimensional CT angiography with volume rendering–comparison with conventional angiographic and surgical findings. Radiology 1999; 211 (02) 497-506
  • 22 Weil AG, Bojanowski MW, Scholtes F, Darsaut TE, Signorelli F, Weill A. Angiographic pitfall: duplicated tapered A1 segment of the anterior cerebral artery mimicking an anterior communicating artery aneurysm. Interv Neuroradiol 2011; 17 (02) 179-182
  • 23 Park J, Kang DH. Infundibular widening mimicking anterior communicating artery aneurysm: report of 2 cases. J Neurosurg 2013; 119 (01) 243-246

Address for correspondence

Eiichi Ishikawa, MD, PhD
Department of Neurosurgery, Faculty of Medicine, University of Tsukuba
2-1-1 Amakubo, Tsukuba, Ibaraki, 305-8576
Japan   

Publikationsverlauf

Artikel online veröffentlicht:
31. März 2023

© 2023. 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/)

Thieme Medical and Scientific Publishers Pvt. Ltd.
A-12, 2nd Floor, Sector 2, Noida-201301 UP, India

  • References

  • 1 Howard BM, Hu R, Barrow JW, Barrow DL. Comprehensive review of imaging of intracranial aneurysms and angiographically negative subarachnoid hemorrhage. Neurosurg Focus 2019; 47 (06) E20
  • 2 Tsunou K, Yamanaka R. Usefulness of the low tube voltage scan in the head CT-angiography with the subarachnoid hemorrhage. Journal of Japanese Society for Emergency Medicine. 2018; 21: 672-679
  • 3 Choi JH, Jo KII, Kim KH. et al. Morphological risk factors for the rupture of anterior communicating artery aneurysms: the significance of fenestration. Neuroradiology 2016; 58 (02) 155-160
  • 4 Cooke DL, Stout CE, Kim WT. et al. Cerebral arterial fenestrations. Interv Neuroradiol 2014; 20 (03) 261-274
  • 5 Osborn AG. Diagnostic Cerebral Angiography. 2nd ed. Philadelphia: Lippincott Williams & Wilkins; 1999: 105-116
  • 6 López-Sala P, Alberdi N, Mendigaña M, Bacaicoa MC, Cabada T. Anatomical variants of anterior communicating artery complex. A study by computerized tomographic angiography. J Clin Neurosci 2020; 80: 182-187
  • 7 Kwak R, Niizuma H, Hatanaka M, Suzuki J. Anterior communicating artery aneurysms accompanied with anomalies or anterior communicating artery (author's transl) [article in Japnese]. No To Shinkei 1978; 30 (11) 1221-1225
  • 8 Kwak R, Niizuma H, Hatanaka M, Suzuki J. Anterior communicating artery aneurysms with associated anomalies. J Neurosurg 1980; 52 (02) 162-164
  • 9 Cai W, Hu C, Gong J, Lan Q. Anterior communicating artery aneurysm morphology and the risk of rupture. World Neurosurg 2018; 109: 119-126
  • 10 Sailer AM, Wagemans BA, Nelemans PJ, de Graaf R, van Zwam WH. Diagnosing intracranial aneurysms with MR angiography: systematic review and meta-analysis. Stroke 2014; 45 (01) 119-126
  • 11 Chappell ET, Moure FC, Good MC. Comparison of computed tomographic angiography with digital subtraction angiography in the diagnosis of cerebral aneurysms: a meta-analysis. Neurosurgery 2003; 52 (03) 624-631 , discussion 630–631
  • 12 Menke J, Larsen J, Kallenberg K. Diagnosing cerebral aneurysms by computed tomographic angiography: meta-analysis. Ann Neurol 2011; 69 (04) 646-654
  • 13 White PM, Wardlaw JM, Easton V. Can noninvasive imaging accurately depict intracranial aneurysms? A systematic review. Radiology 2000; 217 (02) 361-370
  • 14 Bernstein MA, Huston III J, Lin C, Gibbs GF, Felmlee JP. High-resolution intracranial and cervical MRA at 3.0T: technical considerations and initial experience. Magn Reson Med 2001; 46 (05) 955-962
  • 15 Tang PH, Hui F, Sitoh YY. Intracranial aneurysm detection with 3T magnetic resonance angiography. Ann Acad Med Singap 2007; 36 (06) 388-393
  • 16 Serizawa T, Saeki N, Yamaura A. Microsurgical anatomy and clinical significance of the anterior communicating artery and its perforating branches. Neurosurgery 1997; 40 (06) 1211-1216 , discussion 1216–1218
  • 17 Sebök M, Dufour JP, Cenzato M. et al. When is diagnostic subtraction angiography indicated before clipping of unruptured and ruptured intracranial aneurysms? An international survey of current practice. Acta Neurochir Suppl (Wien) 2021; 132: 9-17
  • 18 Turan N, Heider RA, Roy AK. et al. Current perspectives in imaging modalities for the assessment of unruptured intracranial aneurysms: a comparative analysis and review. World Neurosurg 2018; 113: 280-292
  • 19 Okahara M, Kiyosue H, Yamashita M. et al. Diagnostic accuracy of magnetic resonance angiography for cerebral aneurysms in correlation with 3D-digital subtraction angiographic images: a study of 133 aneurysms. Stroke 2002; 33 (07) 1803-1808
  • 20 Pradilla G, Wicks RT, Hadelsberg U. et al. Accuracy of computed tomography angiography in the diagnosis of intracranial aneurysms. World Neurosurg 2013; 80 (06) 845-852
  • 21 Korogi Y, Takahashi M, Katada K. et al. Intracranial aneurysms: detection with three-dimensional CT angiography with volume rendering–comparison with conventional angiographic and surgical findings. Radiology 1999; 211 (02) 497-506
  • 22 Weil AG, Bojanowski MW, Scholtes F, Darsaut TE, Signorelli F, Weill A. Angiographic pitfall: duplicated tapered A1 segment of the anterior cerebral artery mimicking an anterior communicating artery aneurysm. Interv Neuroradiol 2011; 17 (02) 179-182
  • 23 Park J, Kang DH. Infundibular widening mimicking anterior communicating artery aneurysm: report of 2 cases. J Neurosurg 2013; 119 (01) 243-246

Zoom Image
Fig. 1 Magnetic resonance (MR) angiography (upper) and its source image (lower) were taken at the age of 44 (A), 49 (B), and 51 (C) years. The 1.5 Tesla MR angiography showing no obvious aneurysm (A). The 3.0 Tesla MR angiography showing an aneurysm (arrow) arising from the anterior communicating artery complex (B, C). The initial MR angiographs point to an aneurysm arising from the complex of the anterior communicating artery (B, C).
Zoom Image
Fig. 2 The three-dimensional computed tomography (CT) angiography (A; lateral view, B; A-P view) showing suspected aneurysm (arrow) arising from the right A1-A2 junction. The source image of the CT angiography also showing the lesion arising from the anterior communicating artery complex.
Zoom Image
Fig. 3 Intraoperative images showing fenestrated anterior communicating artery (AComA) complex with no obvious aneurysm (dotted line: fenestrated AComA, arrow: right A1 segment, arrowhead: left A1 segment, double arrowhead: left A2 segment, white asterisk: fenestration). The magnified view (right) with the vessels forming the fenestration showing dilatation and meandering with pronounced atherosclerosis. The right A2 segment (double arrow) and a small aneurysm-like bulge (black asterisk) with strong arteriosclerosis in the right A2- fenestrated AComA junction were also found.
Zoom Image
Fig. 4 Review of original MR angiography images taken at the age of 51 years with a suspected secant line in an aneurysm-like lesion (arrow).