Next Article in Journal
RETRACTED: Bouam et al. Rapid Isothermal Amplification for the Buccal Detection SARS-CoV-2 in the Context of Out-Patient COVID-19 Screening. J. Clin. Med. 2021, 10, 2643
Previous Article in Journal
Comment on Benekos et al. Intraocular Pressure Reduction Following Phacoemulsification in Patients with Exfoliation: A Systematic Review and Meta-Analysis. J. Clin. Med. 2024, 13, 6774
 
 
Font Type:
Arial Georgia Verdana
Font Size:
Aa Aa Aa
Line Spacing:
Column Width:
Background:
Case Report

Carotid Web as a Cause of Ischemic Stroke: Effective Treatment with Endovascular Techniques

by
Magdalena Konieczna-Brazis
1,
Pawel Brazis
2,*,
Milena Switonska
1 and
Arkadiusz Migdalski
2
1
Department of Neurology and Clinical Neurophysiology, Jan Biziel University Hospital No. 2, Collegium Medicum in Bydgoszcz, Nicolaus Copernicus University in Torun, Poland, Ujejskiego Street 75, 85-168 Bydgoszcz, Poland
2
Department of Vascular Surgery and Angiology, University Hospital No. 1, Collegium Medicum in Bydgoszcz, Nicolaus Copernicus University in Torun, Poland, M. Sklodowskiej-Curie Street 9, 85-094 Bydgoszcz, Poland
*
Author to whom correspondence should be addressed.
J. Clin. Med. 2025, 14(8), 2568; https://doi.org/10.3390/jcm14082568
Submission received: 11 February 2025 / Revised: 6 April 2025 / Accepted: 7 April 2025 / Published: 9 April 2025
(This article belongs to the Topic Diagnosis and Management of Acute Ischemic Stroke)

Abstract

:
Background: Carotid web (CaW) usually presents as a shelf-like intimal flap at the beginning of the internal carotid artery. It has been proven that CaW is associated with ischemic stroke, particularly in young patients without other risk factors. This case report aimed to describe the carotid web that causes ischemic stroke due to embolic complications. Moreover, both pathologies were successfully treated with endovascular techniques in the presented case study. Methods: A 59-year-old male presented to the neurological department with motor aphasia, right-sided weakness, and hypoesthesia. Computer tomography (CT) of the head and computed tomography angiography (CTA) of the aortic arch and intracranial arteries were performed. Due to the unknown onset of the presented stroke symptoms, diagnostics were extended to magnetic resonance (MR), and based on this, the patient qualified for immediate mechanical thrombectomy (according to the DAWN trial protocol). Intraoperative digital subtraction angiography (DSA) revealed embolism material in the left middle cerebral artery (segment M1). The artery was recanalized via aspiration thrombectomy using the Penumbra system, and complete restoration of flow was obtained (according to the TICI scale). In addition, DSA revealed the presence of CaW changes in the left internal carotid artery (LICA). In the control CT scanning, an acute ischemic area in the left temporal lobe was found. After the treatment, the patient demonstrated complete neurological improvement from his initial presentation. He qualified for carotid artery stenting of the LICA, which was postponed to a later period due to the presence of an area of infarction. The angioplasty with stenting was performed 6 months later, and a carotid antiembolic “mesh” stent (Roadsaver, Terumo) was implanted into the LICA across the carotid web. Conclusions: CaW should be considered in the case of stroke resulting from unknown causes. The presented case study demonstrated that both carotid web and ischemic stroke pathologies can be effectively treated with emerging endovascular techniques.

1. Introduction

Carotid web (CaW), also known as carotid diaphragm, is an unusual variant of fibro-muscular dysplasia (FMD). CaW is specified by the fibrous intimal flap, located on the posterior wall of the carotid bulb. The development of thrombogenesis behind the intimal flap is usually associated with an increased risk of cerebral embolic stroke [1].
Although the incidence of CaW is rare, a strong relationship between this change and stroke has been shown, especially in young patients without other vascular conditions. A study showed that CaW occurred in 7/576 (1.2%) patients with suspected stroke during a hospital-based period and indicated that it may be a reasonable expectation in 2.5–37% of cryptogenic strokes [2,3,4,5,6]. CaW is also characterized by a high percentage of recurrent stroke, with a rate of about 27% at 5 years if conservative treatment is used [5].
Endovascular treatment significantly reduces the risk of recurrent stroke. In such cases, angioplasty with stenting is a notably minimally invasive and relatively safe procedure. There is no significant narrowing of the vessel in the place of the CaW, which significantly facilitates the passage of the guidewire and stent implantation [7].
We present a CaW case complicated by acute ischemic stroke of the left-brain hemisphere as a result of the occluded middle cerebral artery (MCA). In the first stage, the patient was treated with intracranial thrombectomy, and then in the second stage, carotid angioplasty with stenting (CAS) was performed. The treatment strategies applied in both phases were shown to be effective and promising.

2. Case History

A 59-year-old male with a history of arterial hypertension and hyperlipidemia was transferred to our Department of Neurology at the Center of Interventional Treatment of Stroke due to motor aphasia, right-sided weakness, and hypoesthesia. The patient awoke with neurological symptoms on the day of admission.
Computer tomography (CT) of the head and computed tomography angiography (CTA) of the aortic arch and intracranial arteries were performed. The patient did not qualify for thrombolysis because of the occlusion of the intracranial artery and the unknown time of the onset of stroke. The diagnostics were extended to magnetic resonance (MR), and based on this, the patient qualified for immediate mechanical thrombectomy according to the DAWN trial protocol (NIHSS scale: 11; DWI MRI: 9 mL) [8].
Digital subtraction angiography (DSA) revealed the embolism material in the M1 section of the left middle cerebral artery (LMCA). The artery was recanalized via aspiration thrombectomy using the Penumbra system, and complete restoration of flow was obtained (according to the Thrombolysis in Cerebral Infarction scale, TICI scale 3) [9], as shown in Figure 1a,b.
In addition, CTA revealed the presence of carotid web changes in the left internal carotid artery (LICA), as shown in Figure 2a,b.
In the control CT scanning, an acute ischemic area in the left temporal lobe was found, as shown in Figure 3.
After the treatment, the patient demonstrated complete neurological improvement from his initial presentation of right weakness, hypoesthesia, and motor aphasia, with no residual deficit.
In additional studies, such as fasting blood sugar, LDL cholesterol, triglycerides, echocardiography, and Holter monitor, no significant pathologies were found. Duplex scan images showed a thickening of the intima–media complex in the LICA. In the secondary prevention period, double-platelet therapy (clopidogrel 75 mg and acetylsalicylic acid 75 mg) and statin treatment (atorvastatin 40 mg) were implemented.
The patient received consultations from a cardiologist and a vascular surgeon. The patient then qualified for carotid artery stenting (CAS) of the LICA, which was postponed to a later period due to the presence of an area of infarction. The angioplasty with stenting was performed 6 months later, and a carotid antiembolic “mesh” stent (Roadsaver, Terumo) was implanted into the LICA across the web with good vascular effect, as shown in Figure 4a,b.

3. Discussion

The literature clearly indicates that CaW is usually found in young patients under 60 years of age [10,11]. Our patient also belongs to this age group. In the case series study published by Multon et al., the median age among 11 symptomatic CaW patients was 41 years (range: 39–51 years) [12]. However, the youngest patient’s description of symptomatic CaW was reported by Kyaw et al. A 20-year-old female presented ischemic stroke symptoms related to the region of the ipsilateral middle cerebral artery [13].
Although CaW is usually associated with the female sex [1,3,14,15,16], in some studies, males and females show similarity [2,5,11].
The pathogenesis of CaW is not clearly explained. Genetic reasons, trauma mechanisms, or hormonal disorders are suspected [17]. The presentation of CaW is most often one-sided and located on the posterior wall of the internal carotid artery (ICA). In the study published by Rzepka M. et al., among 181 patients with acute ischemic stroke or TIA, CaW was found in 27, giving a prevalence of 14.9%. In 16/27, CaW was on the left side; in 9/27, on the right side; and in 2/27, bilateral [18].
Unlike typical FMD, changes in CaW cover only the intima of the artery and do not reach the media [19,20]. In this location, a small valve usually appears, where clots are formed as a result of the slowed blood flow. Such conditions may lead to embolization and ischemic stroke, especially when large intracranial vessels are involved [4,7,19,21]. This is in accordance with the results of a single-center study involving 466 patients with anterior circulation ischemic stroke. Ipsilateral CaW was more frequent in embolic stroke of unknown source than in the rest of the sample (10.7% (confidence interval 95% = 2.7–18.7) vs. 0.7% (0–1.5), p < 0.001). This difference remained significant after adjustment for sex, age, and vascular risk factors (odds ratio: 12.5 (2.1–72), p = 0.005) or after the exclusion of patients with any other bulb wall thickening (p = 0.025) [21].
Our patient experienced an ischemic stroke as a result of an occluded MCA. The stroke occurred on the same side as the CaW location, and no other possible causes were found.
According to Tabibian BE et al., the size and morphology of CaW may be associated with the risk of stroke. The authors concluded that such morphological features of CaW as a length ≥ 3 mm, an acute angle relative to the carotid wall, a thickness ≥ 1.85 mm, and stenosis of lumen > 50% were present more often in symptomatic patients compared with asymptomatic. However, vessel narrowing caused by CaW may be a doubtful parameter in relation to stroke occurrence [22]. Kim SJ et al. examined patients with cryptogenic stroke and found that symptomatic CaW formed less than 30% of the degree of stenosis [23].
In the performed imaging studies before the intervention, the CaW change was detected only in the CTA with morphology suitable for the features mentioned above.
In the Duplex scan images, only local non-specific thickening of the wall was found, which is consistent with other reports. Duplex scanning alone is insufficient for recognizing CaW, as it is easy to confuse this pathology with atherosclerotic plaque. Therefore, CTA remains a gold diagnostic standard and is considered the first-line diagnostic modality [16,20,24].
CaW pathology is best viewed in an oblique projection using the multiplanar reconstruction (MPR) technique. Moreover, it should be differentiated from atherosclerotic plaque, dissection, and FMD [7]. Atherosclerotic plaque is rarely limited to the posterior wall; its surface is often irregular and calcified and covers the entire circumference of the vessel. Dissection, in turn, most often includes a longer section of the artery, below and above the carotid bulb. FMD usually affects the middle section of the ICA [25,26,27].
In our case, in an acute phase of stroke, we performed an intracranial endovascular treatment. The patient was enrolled for such treatment according to the DAWN protocol, based on imaging studies and a therapeutic window between 6 and 24 h [8]. DSA showed embolism deposits in the LMCA, which were removed using aspiration thrombectomy. This technique is considered a therapeutic option for patients with stroke due to intracranial atherosclerotic and embolic large vessel occlusion. In both etiologies, the results regarding recanalization, favorable outcomes (at 90 days), and mortality (at 90 days) are comparable [28]. After the stroke episode, we commenced double-platelet therapy. This pharmacological therapy is preferred as the initial treatment in both asymptomatic and symptomatic CaW [11].
In observational studies, the risk of the recurrence of stroke in symptomatic CaW is 17% over 2 years [29]. This was also proven in a systematic review of CaW therapies published by Zhang et al. The authors identified 135 patients with symptomatic CaW, and those who were not treated with invasive techniques had a 56% rate of recurrent stroke. In the subgroup that received carotid intervention (CEA or CAS), no recurrent strokes were observed [15]. Therefore, invasive treatment should be offered to these patients. Surgical endarterectomy can be technically difficult, as there is usually no significant narrowing in the CaW location. The only advantage of this method is the histopathological evaluation of excised tissue [7].
Angioplasty with stenting is a remarkable and less invasive technique. The validity of this method was confirmed in a study of symptomatic patients with stent implantation across the CaW lesion. No patient had a recurrent stroke during the 12-month follow-up period [11,30]. In our case, a mesh stent (Roadsaver, Terumo) with a double layer dedicated to thrombogenic changes was successfully implanted [31,32].
The number of published CaW case reports is growing. Authors are beginning to pay special attention to CaW as a cause of stroke. We are currently observing significant developments of endovascular techniques and products that can be effectively used to treat both stroke and CaW lesions. Our study is a case in point of this. The extended therapeutic window after stroke allowed for aspiration thrombectomy with an excellent clinical effect. In turn, we believe that the stent treatment of CaW lesions is a much better solution than endarterectomy. Table 1 presents a summary of published CaW case reports. While some authors reported stent implantation, only two studies specified the type of stent used. Our patient was ultimately treated with the dual-layer stent, which allows appropriate radial force to be applied to arterial wall and limits the risk of thrombo-embolism complications with its dense mesh structure. Nevertheless, future registry is required to assess the safety and efficacy of mesh stent use in CaW.

4. Conclusions

CaW should be considered in the case of stroke resulting from unknown causes. Moreover, imaging studies performed during stroke diagnostics require precise attention to CaW changes. The case presented in this study demonstrates that CaW with subsequent stroke due to the occlusion of the MCA can be effectively treated with emerging endovascular techniques.

Author Contributions

Conceptualization, M.K.-B. and P.B.; methodology, P.B. and M.K.-B.; soft-ware, M.K.-B. and P.B.; formal analysis M.K.-B. and P.B.; investigation M.K.-B. and P.B.; data curation, M.K.-B. and P.B.; writing—original draft preparation, M.K.-B. and P.B.; writing—review and editing, P.B. and M.K.-B.; supervision, P.B., M.K.-B., M.S. and A.M. All authors have read and agreed to the published version of the manuscript.

Funding

There were no sources of funding for this study.

Institutional review Board Statement

Ethical review and approval were waived for this study because the patient did not require the consent of the Ethics Committee or Institutional Review Board to describe his case. His image and personal data were not used for this purpose.

Informed Consent Statement

The patient provided his written informed consent for data collection on admission.

Data Availability Statement

All the data and models that support the findings of this study are available from the corresponding author upon reasonable request.

Conflicts of Interest

The authors declare no conflicts of interest.

References

  1. Mac Grory, B.; Emmer, B.J.; Roosendaal, S.D.; Zagzag, D.; Yaghi, S.; Nossek, E. Carotid web: An occult mechanism of embolic stroke. J. Neurol. Neurosurg. Psychiatry 2020, 91, 1283–1289. [Google Scholar] [CrossRef] [PubMed]
  2. Choi, P.M.; Singh, D.; Trivedi, A.; Qazi, E.; George, D.; Wong, J.; Demchuk, A.M.; Goyal, M.; Hill, M.D.; Menon, B.K. Carotid Webs and Recurrent Ischemic Strokes in the Era of CT Angiography. Am. J. Neuroradiol. 2015, 36, 2134–2139. [Google Scholar] [CrossRef]
  3. Compagne, K.C.J.; van Es, A.C.G.M.; Berkhemer, O.A.; Borst, J.; Roos, Y.B.W.E.M.; van Oostenbrugge, R.J.; van Zwam, W.H.; Majoie, C.B.L.M.; Marquering, H.A.; Dippel, D.W.J.; et al. Prevalence of Carotid Web in Patients with Acute Intracranial Stroke Due to Intracranial Large Vessel Occlusion. Radiology 2018, 286, 1000–1007. [Google Scholar] [CrossRef] [PubMed]
  4. Turpinat, C.; Collemiche, F.L.; Arquizan, C.; Molinari, N.; Cagnazzo, F.; Mourand, I.; Lefèvre, P.H.; Henneton, P.; Corti, L.; Gascou, G.; et al. Prevalence of carotid web in a French cohort of cryptogenic stroke. J. Neurol. Sci. 2021, 427, 117513. [Google Scholar] [CrossRef]
  5. Olindo, S.; Chausson, N.; Signate, A.; Mecharles, S.; Hennequin, J.-L.; Saint-Vil, M.; Edimonana-Kaptue, M.; Jeannin, S.; Landais, A.; Cabre, P.; et al. Stroke Recurrence in First-Ever Symptomatic Carotid Web: A Cohort Study. J. Stroke 2021, 23, 253–262. [Google Scholar] [CrossRef] [PubMed]
  6. Joux, J.; Boulanger, M.; Jeannin, S.; Chausson, N.; Hennequin, J.-L.; Molinié, V.; Smadja, D.; Touzé, E.; Olindo, S. Association Between Carotid Bulb Diaphragm and Ischemic Stroke in Young Afro-Caribbean Patients. Stroke 2016, 47, 2641–2644. [Google Scholar] [CrossRef]
  7. Chen, H.; Colasurdo, M.; Costa, M.; Nossek, E.; Kan, P. Carotid webs: A review of pathophysiology, diagnostic findings, and treatment options. J. Neurointerv. Surg. 2024, 16, 1294–1299. [Google Scholar] [CrossRef]
  8. Nogueira, R.G.; Jadhav, A.P.; Haussen, D.C.; Bonafe, A.; Budzik, R.F.; Bhuva, P.; Yavagal, D.R.; Ribo, M.; Cognard, C.; Hanel, R.A.; et al. Thrombectomy 6 to 24 Hours after Stroke with a Mismatch between Deficit and Infarct. N. Engl. J. Med. 2018, 378, 11–21. [Google Scholar] [CrossRef]
  9. Zaidat, O.O.; Yoo, A.J.; Khatri, P.; Tomsick, T.A.; von Kummer, R.; Saver, J.L.; Marks, M.P.; Prabhakaran, S.; Kallmes, D.F.; Fitzsimmons, B.-F.M.; et al. Recommendations on Angiographic Revascularization Grading Standards for Acute Ischemic Stroke. Stroke 2013, 44, 2650–2663. [Google Scholar] [CrossRef]
  10. Sajedi, P.I.; Gonzalez, J.N.; Cronin, C.A.; Kouo, T.; Steven, A.; Zhuo, J.; Thompson, O.; Castellani, R.; Kittner, S.J.; Gandhi, D.; et al. Carotid Bulb Webs as a Cause of “Cryptogenic” Ischemic Stroke. Am. J. Neuroradiol. 2017, 38, 1399–1404. [Google Scholar] [CrossRef]
  11. Haussen, D.C.; Grossberg, J.A.; Koch, S.; Malik, A.; Yavagal, D.; Gory, B.; Leesch, W.; Hassan, A.E.; Derelle, A.-L.; Richard, S.; et al. Multicenter Experience with Stenting for Symptomatic Carotid Web. Interv. Neurol. 2018, 7, 413–418. [Google Scholar] [CrossRef] [PubMed]
  12. Multon, S.; Denier, C.; Charbonneau, P.; Sarov, M.; Boulate, D.; Mitilian, D.; Mougin, J.; Chassin, O.; Legris, N.; Fadel, E.; et al. Carotid webs management in symptomatic patients. J. Vasc. Surg. 2020, 73, 1290–1297. [Google Scholar] [CrossRef]
  13. Kyaw, K.; Latt, H.; Aung, S.S.M.; Babu, J.; Rangaswamy, R. A rare case of carotid web presenting with ischemic stroke in a young woman and a brief review of the literature. Case Rep. Med. 2018, 2018, 3195679. [Google Scholar] [CrossRef] [PubMed]
  14. El-Masri, S.; Wilson, M.M.; Kleinig, T. Systematic review and meta-analysis of ipsilateral and contralateral carotid web prevalence in embolic supratentorial strokes of undetermined source. J. Clin. Neurosci. 2022, 107, 118–123. [Google Scholar] [CrossRef]
  15. Zhang, A.J.; Dhruv, P.; Choi, P.; Bakker, C.; Koffel, J.; Anderson, D.; Kim, J.; Jagadeesan, B.; Menon, B.K.; Streib, C. A Systematic Literature Review of Patients With Carotid Web and Acute Ischemic Stroke. Stroke 2018, 49, 2872–2876. [Google Scholar] [CrossRef] [PubMed]
  16. Fontaine, L.; Guidolin, B.; Viguier, A.; Gollion, C.; Barbieux, M.; Larrue, V. Ultrasound characteristics of carotid web. J. Neuroimaging 2022, 32, 894–901. [Google Scholar] [CrossRef]
  17. Olin, J.W.; Gornik, H.L.; Bacharach, J.M.; Biller, J.; Fine, L.J.; Gray, B.H.; Gray, W.A.; Gupta, R.; Hamburg, N.M.; Katzen, B.T.; et al. Fibromuscular Dysplasia: State of the Science and Critical Unanswered Questions. Circulation 2014, 129, 1048–1078. [Google Scholar] [CrossRef]
  18. Rzepka, M.; Chmiela, T.; Bosowska, J.; Cebula, M.; Krzystanek, E. Fibromuscular Dysplasia/Carotid Web in Angio-CT Imaging: A Rare Cause of Ischemic Stroke. Medicina 2021, 57, 1112. [Google Scholar] [CrossRef]
  19. Kim, S.J.; Nogueira, R.G.; Haussen, D.C. Current Understanding and Gaps in Research of Carotid Webs in Ischemic Strokes: A Review. JAMA Neurol. 2019, 76, 355–361. [Google Scholar] [CrossRef]
  20. Liang, S.; Qin, P.; Xie, L.; Niu, S.; Luo, J.; Chen, F.; Chen, X.; Zhang, J.; Wang, G. The carotid web: Current research status and imaging features. Front. Neurosci. 2023, 17, 1104212. [Google Scholar] [CrossRef]
  21. Labeyrie, M.-A.; Serrano, F.; Civelli, V.; Jourdaine, C.; Reiner, P.; Saint-Maurice, J.-P.; Chabriat, H.; Houdart, E. Carotid artery webs in embolic stroke of undetermined source with large intracranial vessel occlusion. Int. J. Stroke 2020, 16, 392–395. [Google Scholar] [CrossRef] [PubMed]
  22. Tabibian, B.E.; Parr, M.; Salehani, A.; Mahavadi, A.; Rahm, S.; Kaur, M.; Howell, S.; Jones, J.G.; Liptrap, E.; Harrigan, M.R. Morphological characteristics of symptomatic and asymptomatic carotid webs. J. Neurosurg. 2022, 137, 1727–1732. [Google Scholar] [CrossRef] [PubMed]
  23. Kim, S.J.; Allen, J.W.; Bouslama, M.; Nahab, F.; Frankel, M.R.; Nogueira, R.G.; Haussen, D.C. Carotid Webs in Cryptogenic Ischemic Strokes: A Matched Case-Control Study. J. Stroke Cerebrovasc. Dis. 2019, 28, 104402. [Google Scholar] [CrossRef] [PubMed]
  24. Madaelil, T.P.; Grossberg, J.A.; Nogueira, R.G.; Anderson, A.; Barreira, C.; Frankel, M.; Haussen, D.C. Multimodality Imaging in Carotid Web. Front. Neurol. 2019, 10, 220. [Google Scholar] [CrossRef]
  25. Zelada-Ríos, L.; Barrientos-Imán, D.; Simbrón-Ribbeck, L.; Argomedo, C.A.; Ramírez-Quiñones, J.; La Rosa, P.C.; Chávez, A.V.; Otiniano-Sifuentes, R. Importance of multiplanar reformation angiographic images for the detection of carotid web. Brain Circ. 2023, 9, 44–47. [Google Scholar] [CrossRef]
  26. Wintermark, M.; Jawadi, S.S.; Rapp, J.H.; Tihan, T.; Tong, E.; Glidden, D.V.; Abedin, S.; Schaeffer, S.; Acevedo-Bolton, G.; Boudignon, B.; et al. High-Resolution CT Imaging of Carotid Artery Atherosclerotic Plaques. Am. J. Neuroradiol. 2008, 29, 875–882. [Google Scholar] [CrossRef]
  27. Sharashidze, V.; Nogueira, R.G.; Al-Bayati, A.R.; Bhatt, N.; Nahab, F.B.; Yun, J.; Allen, J.W.; Frankel, M.; Haussen, D.C. Carotid Web Phenotype Is Uncommonly Associated With Classic Fibromuscular Dysplasia: A Retrospective Observational Study. Stroke 2022, 53, E33–E36. [Google Scholar] [CrossRef]
  28. Zeng, F.; Pan, Q.; Wang, X.; Wang, Z.; Ni, J. The Efficacy and Safety of Endovascular Treatment on Large Vessel Occlusion of Intracranial Atherosclerosis Versus Embolism: A Meta-Analysis. Cardiol. Rev. 2024. [Google Scholar] [CrossRef]
  29. Guglielmi, V.; Compagne, K.C.J.; Sarrami, A.H.; Sluis, W.M.; van den Berg, L.A.; van der Sluijs, P.M.; Mandell, D.M.; van der Lugt, A.; Roos, Y.B.W.E.M.; Majoie, C.B.L.M.; et al. Assessment of Recurrent Stroke Risk in Patients With a Carotid Web. JAMA Neurol. 2021, 78, 826–833. [Google Scholar] [CrossRef]
  30. Haussen, D.C.; Grossberg, J.A.; Bouslama, M.; Pradilla, G.; Belagaje, S.; Bianchi, N.; Allen, J.W.; Frankel, M.; Nogueira, R.G. Carotid Web (Intimal Fibromuscular Dysplasia) Has High Stroke Recurrence Risk and Is Amenable to Stenting. Stroke 2017, 48, 3134–3137. [Google Scholar] [CrossRef]
  31. Marnat, G.; Holay, Q.; Darcourt, J.; Desilles, J.-P.; Obadia, M.; Viguier, A.; Caroff, J.; Denier, C.; Papillon, L.; Barreau, X.; et al. Dual-layer carotid stenting for symptomatic carotid web: Results from the Caroweb study. J. Neuroradiol. 2022, 50, 444–448. [Google Scholar] [CrossRef]
  32. Musiałek, P.; Tekieli, L.; Umemoto, T. Carotid Antiembolic (“Mesh”) Stents: Not Created Equal. J. Soc. Cardiovasc. Angiogr. Interv. 2024, 3, 102429. [Google Scholar] [CrossRef] [PubMed]
  33. Yokoyama, K. Clinical Insights on My Acute Ischemic Stroke Caused by a Carotid Web. Cureus 2024, 16, e76093. [Google Scholar] [CrossRef]
  34. Takahashi, T.; Yanaka, K.; Aiyama, H.; Saura, M.; Kajita, M.; Takahashi, N.; Marushima, A.; Matsumaru, Y.; Ishikawa, E. Spontaneous asymptomatic common carotid artery dissection resembling a carotid web: Illustrative case. J. Neurosurg. Case Lessons 2024, 8, CASE24344. [Google Scholar] [CrossRef] [PubMed]
  35. Wojcik, K.; Milburn, J.; Vidal, G.; Steven, A. Carotid Webs: Radiographic Appearance and Significance. Ochsner J. 2018, 18, 115–120. [Google Scholar] [CrossRef] [PubMed]
  36. Martinez-Perez, R.; Lownie, S.P.; Pandey, S.K.; Boulton, M.R. Stent Placement for Carotid Web. World Neurosurg. 2017, 98, 879.e9–879.e11. [Google Scholar] [CrossRef]
  37. Elmokadem, A.H.; Ansari, S.A.; Sangha, R.; Prabhakaran, S.; Shaibani, A.; Hurley, M.C. Neurointerventional management of carotid webs associated with recurrent and acute cerebral ischemic syndromes. Interv. Neuroradiol. 2016, 22, 432–437. [Google Scholar] [CrossRef]
Figure 1. The first stage of endovascular treatment. Initial angiography of the left middle cerebral artery (LMCA) before (a) and after the thrombectomy (b), showing the achieved complete patency.
Figure 1. The first stage of endovascular treatment. Initial angiography of the left middle cerebral artery (LMCA) before (a) and after the thrombectomy (b), showing the achieved complete patency.
Jcm 14 02568 g001
Figure 2. CT angiography showed a carotid web lesion (CaW) in the LICA (a) and the nest-like (cross-plane, indicated with an arrow) structure in the posterolateral wall of the carotid bulb (b), which is characteristic of CaW.
Figure 2. CT angiography showed a carotid web lesion (CaW) in the LICA (a) and the nest-like (cross-plane, indicated with an arrow) structure in the posterolateral wall of the carotid bulb (b), which is characteristic of CaW.
Jcm 14 02568 g002
Figure 3. Control CT scan after 24 h of LMCA thrombectomy. An ischemic area appeared in the left temporal lobe, which required postponement of the final endovascular procedure.
Figure 3. Control CT scan after 24 h of LMCA thrombectomy. An ischemic area appeared in the left temporal lobe, which required postponement of the final endovascular procedure.
Jcm 14 02568 g003
Figure 4. The second stage of endovascular treatment. Intraoperative angiography with confirmed CaW (indicated by the arrow) pathology (a) and implanted mesh stent across the lesion (b).
Figure 4. The second stage of endovascular treatment. Intraoperative angiography with confirmed CaW (indicated by the arrow) pathology (a) and implanted mesh stent across the lesion (b).
Jcm 14 02568 g004
Table 1. Summary of published CaW case reports.
Table 1. Summary of published CaW case reports.
Case ReportsAgeGenderRaceStrokeCardiovasc. DiseaseDiabetes MellitusSmokingOral
Contracept.
Medical Management of StrokeStroke
Intervention
Carotid InterventionClinical
Outcome
Yokoyama K [33]46MAsianYesNoNoNo-NotPA, MTCEAResidual symptoms
Takahashi T et al. [34]50FAsianYesNoNoNo-NotPA, MT
Decompressive craniectomy
CEAPartial recovery
Kyaw K et al. [13]20FCaucasianYesNoNoNoYesYesNoNoPoor recovery
Wojcik K et al. [35]45F-Yes, r----YesNoCEAPartial recovery
44F-Yes----NotPA, MTCAS *Full recovery
52F-Yes----NotPANoProbable recovery
47M-TIA----YesNoNoFull recovery
51F-Yes----NotPA, MTCASPartial recovery
Martinez-Perez R et al. [36]47F-Yes----NoMTCASFull recovery
Elmokadem AH et al. [37]36M-Yes, rAHNoNo-NoMTCAS *Residual symptoms
41F-Yes, rNoNoNo-NoMTCAS *Residual symptoms
Our case59MCaucasianYesAHNoNo-NoMTCAS **Full recovery
AH—arterial hypertension, tPA—tissue plasminogen activator, MT—mechanical thrombectomy, CEA—carotid endarterectomy, CAS—carotid artery stenting, r—recurrent, * closed cell stent, ** double-layer mesh stent.
Disclaimer/Publisher’s Note: The statements, opinions and data contained in all publications are solely those of the individual author(s) and contributor(s) and not of MDPI and/or the editor(s). MDPI and/or the editor(s) disclaim responsibility for any injury to people or property resulting from any ideas, methods, instructions or products referred to in the content.

Share and Cite

MDPI and ACS Style

Konieczna-Brazis, M.; Brazis, P.; Switonska, M.; Migdalski, A. Carotid Web as a Cause of Ischemic Stroke: Effective Treatment with Endovascular Techniques. J. Clin. Med. 2025, 14, 2568. https://doi.org/10.3390/jcm14082568

AMA Style

Konieczna-Brazis M, Brazis P, Switonska M, Migdalski A. Carotid Web as a Cause of Ischemic Stroke: Effective Treatment with Endovascular Techniques. Journal of Clinical Medicine. 2025; 14(8):2568. https://doi.org/10.3390/jcm14082568

Chicago/Turabian Style

Konieczna-Brazis, Magdalena, Pawel Brazis, Milena Switonska, and Arkadiusz Migdalski. 2025. "Carotid Web as a Cause of Ischemic Stroke: Effective Treatment with Endovascular Techniques" Journal of Clinical Medicine 14, no. 8: 2568. https://doi.org/10.3390/jcm14082568

APA Style

Konieczna-Brazis, M., Brazis, P., Switonska, M., & Migdalski, A. (2025). Carotid Web as a Cause of Ischemic Stroke: Effective Treatment with Endovascular Techniques. Journal of Clinical Medicine, 14(8), 2568. https://doi.org/10.3390/jcm14082568

Note that from the first issue of 2016, this journal uses article numbers instead of page numbers. See further details here.

Article Metrics

Back to TopTop