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International Journal of Medical Sciences logoLink to International Journal of Medical Sciences
. 2019 Jan 1;16(2):203–211. doi: 10.7150/ijms.29637

Current status of endovascular treatment for dural arteriovenous fistulae in the anterior cranial fossa: A systematic literature review

Kan Xu 1,*, Tiefeng Ji 2,*, Chao Li 3, Jinlu Yu 1,
PMCID: PMC6367520  PMID: 30745800

Abstract

Anterior cranial fossa (ACF) dural arteriovenous fistulae (DAVFs) are rare, and a systematic review of the literature is lacking. Such a review is necessary, however, so a systematic PubMed search of related studies was performed. Twenty-four studies were identified, reporting on 48 patients, of whom 39 had definite age and sex information and 33 (84.6%, 33/39) were male. The afflicted patients were between 37 and 80 years old (mean 55.6). Among the 48 patients, 28 (58.3%, 28/48) primarily presented with intracranial hemorrhage, 47 (97.9%, 47/48) had feeding arteries from the anterior ethmoidal artery (AEA) of the ophthalmic artery (OA), and 40 (83.3%, 40/48) had bilateral feeding arteries. All of the cases had high-grade Cognard classifications (III-IV). Among the 48 patients, 43 (89.6%, 43/48) had drainage into the superior sagittal sinus (SSS). In addition, 36 (75%, 36/48) patients were treated via transarterial embolization (TAE). Of these patients, 28 (77.8%, 28/36) were managed via the AEA of the OA. Another 12 (25%, 12/48) patients were treated via transvenous embolization (TVE), 11 of whom (91.7%, 11/12) were treated with the trans-SSS approach. Complete angiographic cure was achieved in 44 (91.7%, 44/48) patients, with 4 (8.3%, 4/48) patients suffering from postprocedural complications. All 48 patients had clear descriptions of follow-up outcomes, with 45 (93.8%, 45/48) patients having a good outcome. Thus, when treating ACF DAVFs, endovascular treatment (EVT) can completely obliterate the fistula point and correct the venous shunting. EVT is therefore an effective treatment for ACF DAVF. Although many complications can occur, this approach achieves good outcomes in most cases.

Keywords: endovascular treatment, dural arteriovenous fistula, anterior cranial fossa, systematic review

Introduction

A dural arteriovenous fistula (DAVF) is an arteriovenous shunt located in the dural wall of the venous sinus or the expanded layer of the dura mater 1-3. Intracranial DAVFs account for only 10% to 15% of intracranial vascular malformations, and only 10% of all DAVFs are located in the anterior cranial fossa (ACF) 4-7. Therefore, the rate of ACF DAVFs is 1% to 1.5% of intracranial vascular malformations, which is very rare.

ACF DAVFs are also termed ethmoidal DAVFs or cribriform plate DAVFs. These vascular events are notorious for their proclivity to drain directly into cortical veins, indicating a malignant natural history and a high bleeding risk in 91% of cases. Hence, ACF DAVFs are usually treated regardless of whether they are symptomatic 4, 8.

Currently, treatments for ACF DAVFs include surgical resection, endovascular treatment (EVT) and stereotactic radiosurgery 9. Surgical resection is very effective because it has low postoperative morbidity and can achieve a complete cure 8, 10. However, surgical resection is also associated with risks inherent to frontal craniotomy, including fontal sinus opening, cerebrospinal fluid leakage, intradural infection, and retraction damage to the frontal lobe and olfactory nerves 11. Radiosurgery has been described as an efficient treatment, but an extended period of time is required to occlude the DAVF 9.

Recently, trends in the management of ACF DAVF have been significantly affected by technological advances in EVT related to the widespread use of new microcatheters, and morbidity and modality have apparently been reduced 8. Since its introduction in 2000, the Onyx Liquid Embolic System (Irvine, CA, USA) has been widely used for embolization in DAVFs and is easier to control than previously available liquid agents 12, 13. EVT, including transarterial embolization (TAE) and transvenous embolization (TVE), is currently considered the first therapeutic option for ACF DAVFs 14, 15.

Current data regarding EVT for ACF DAVFs are sporadic. No systematic review of EVT for ACF DAVFs has previously been published; hence, we reviewed the available literature on this subject. Literature searches identified 48 cases of EVT for ACF DAVFs, which are shown in Table 1. Meanwhile, general and angiographic data on the ACF DAVF series are summarized in Table 2. In this article, EVT for ACF DAVFs is the primary focus of the systematic literature review.

Table 1.

Clinical data for patients with EVT for ACF DAVF

No. Author/Year Age/Sex Presentation Feeding arteries Venous drainage Cognard type EVT Angiographic cure Complication Outcome
1 Matsumaru et al./199717 62/M IH Bilateral AEA of the OA Frontal vein to the SSS III TAE: via both AEAs of the OAs with NBCA Complete No Good
2 Defreyne et al./200011 40/M SAH Bilateral AEA of the OA; Ethmoidal branches of the IMA Frontal vein to the SSS III TVE: trans-SSS approach with coils. Complete No Good
3 Defreyne et al./200011 39/M Asymptomatic Bilateral AEA of the OA Frontal vein to the SSS; Basal vein of Rosenthal IV TVE: trans-SSS approach with coils. Complete No Good
4 Abrahams et al./200218 77/M Dementia Bilateral AEA of the OA; Ethmoidal branches of the IMA and MMA Frontal vein to the SSS IV TAE: via ethmoidal branches of the IMA or MMA Incomplete No Good
5 Flynn et al./200719 39/F IH Unilateral AEA of the OA Basal vein of Rosenthal IV TAE: via the AEA of the OA with NBCA Complete No Good
6 Lv et al./200720 52/M IH Bilateral AEA of the OA and ethmoidal branches of the IMA Frontal vein to the SSS IV TAE: via both AEAs of the OA with Onyx, two stages. Complete No Good
7 Katsaridis et al./200721 76/M IH Bilateral AEAs of the OAs Frontal vein to the SSS IV TAE: via both AEAs of the OAs with NBCA Complete No Good
8 Lv et al./200822 65/M Dementia and seizure Unilateral AEA of the OA and ethmoidal branches of the IMA Frontal vein to the SSS III TAE: via the AEA of the OA with Onyx.
TVE: trans-SSS approach with coils.
Complete No Good
9 Lv et al./200823 48/M Headache and blurred vision Bilateral AEA of the OA, ethmoidal branches of the IMA and MMA Frontal vein to the SSS III TVE: trans-SSS approach with coils. Complete No Good
10 Lv et al./200823 60/M IH Bilateral AEAs of the OAs Frontal vein to cavernous sinus IV TAE: via the AEA of the OA with Onyx Complete No Good
11 Tahon et al./200824 50/M Headache Bilateral AEA of the OA and MMA, both pial branches of the ACA and MCA Frontal vein to the SSS; Basal vein of Rosenthal IV TAE: via the MMA with Onyx Complete No Good
12 Tsutsumi et al./200925 59/M IH Bilateral AEA of the OA; Unilateral persistent primitive olfactory artery Frontal vein to the SSS III TAE: via persistent primitive olfactory artery and AEA of the OA with NBCA Incomplete No Good
13 Agid et al./20099 55/M IH Bilateral AEA of the OA; Ethmoidal branches of the IMA Frontal vein to the SSS IV TAE: via the AEA of the OA with NBCA Complete No Good
14 Guedin et al./201026 75/M IH Unilateral the PEA of the OA Frontal vein to the SSS IV TAE: via the PEA of the OA with Onyx Complete No Good
15 Ishihara et al./201027 71/M Blurred vision Bilateral facial arteries; Unilateral AEA of the OA Frontal vein to the SSS III TAE: via facial artery with NBCA Complete No Good
16 Mack et al./201128 57/M SAH Bilateral AEA of the OA and ethmoidal branches of the IMA Frontal vein to the SSS IV TAE: via the AEA of the OA with Onyx Complete No Good
17 Mack et al./201128 54/F Headache and vision impairment Bilateral AEA and the PEA of the OA Basal vein of Rosenthal IV TAE: via both AEAs of the OA with NBCA and Onyx Complete Edema of thalamus/ midbrain IM
18 Zhao et al./201229 58/M SDH Unilateral AEA of the OA Frontal vein to the SSS IV TAE: via the AEA of the OA with Onyx. Complete No Good
19 Li et al./201312 37/M SAH Bilateral AEA of the OA; Branch of the facial artery; MMA Frontal vein to the SSS IV TAE: via the AEA of the OA and branch of the facial artery with Onyx, twice stages. Incomplete Excessive reflux Good
20 Li et al./201312 52/M Blurred vision Bilateral AEA of the OA; Pial branch of the ACA Frontal vein to the SSS III TAE: via AEA of the OA with Onyx. Complete No Good
21 Li et al./201312 68/M IH, IVH Bilateral AEA of the OA; Ethmoidal branches of the IMA Frontal vein to the SSS IV TAE: via the AEA of the OA with Onyx. Complete No Worse
22 Li et al./201312 60/M IH, SDH Bilateral AEA of the OA; Ethmoidal branches of the IMA Frontal vein to the SSS IV TAE: via the AEA of the OA with Onyx. Complete No Good
23 Li et al./201312 54/M SAH Bilateral AEA of the OA; Pial branch of the ACA Frontal vein to the SSS IV TAE: via the AEA of the OA with Onyx. Complete No Good
24 Li et al./201312 43/M IH, IVH Bilateral AEA of the OA; MMA Frontal vein to the SSS IV TAE: via AEA of the OA with Onyx. Complete No Good
25 Li et al./201312 55/M IH, IVH Bilateral AEA of the OA Frontal vein to the SSS III TAE: via the AEA of the OA with Onyx. Complete Excessive reflux Good
26 Li et al./201312 57/F SAH Bilateral AEA of the OA; Ethmoidal branches of the IMA Frontal vein to the SSS IV TAE: via the AEA of the OA with Onyx. Complete No Good
27 Li et al./201312 40/M Headache Bilateral AEA of the OA; Branches of the facial artery Frontal vein to the SSS IV TAE: via AEA of the OA with Onyx. Complete No Good
28 Li et al./201312 37/M IH, SDH Bilateral AEA of the OA; Branches of the facial artery; MMA Frontal vein to the SSS III TAE: via the AEA of the OA with Onyx. Complete No Good
29 Li et al./201312 42/M IH, IVH Bilateral AEA of the OA Frontal vein to the SSS IV TAE: via the AEA of the OA with Onyx. Complete No Good
30 Li et al./201430 NM
(range: 38-68)
IH Unilateral AEA of the OA, ethmoidal branches of the IMA and MMA Frontal vein to the SSS III or IV TAE: via AEA of the OA with Onyx. Incomplete No Good
31 Li et al./201430 NM
(range: 38-68)
IH Unilateral AEA of the OA and ethmoidal branch of the IMA; Bilateral pial branches of the ACAs Frontal vein to the SSS III or IV TAE: via the MMA and pial branches of the ACAs with Onyx. Complete Microcatheter entrapment Good
32 Li et al./201430 NM
(range: 38-68)
IH, IVH Bilateral AEA of the OA Frontal vein to the SSS; inferior frontal vein into the sylvian veins IV TAE: via both AEAs of the OAs with Onyx. Complete No Good
33 Li et al./201430 NM
(range: 38-68)
IH Bilateral AEA of the OA, unilateral ethmoidal branch of the IMA Frontal vein to the SSS; Ophthalmic vein III or IV TAE: via both AEAs of the OAs with Onyx. Complete No Good
34 Li et al./201430 NM
(range: 38-68)
Asymptomatic Bilateral AEA of the OA Frontal vein to the SSS; Basal vein of Rosenthal IV TAE: via the AEA of the OA with Onyx. Complete No Good
35 Li et al./201430 NM
(range: 38-68)
IH Bilateral AEA of the OA Inferior frontal cortical vein into the sylvian veins III or IV TAE: via the AEA of the OA with Onyx. Complete No Good
36 Spiotta et al./201431 41/M Headache and blurred vision Bilateral AEA of the OA Frontal vein to the SSS III TAE: via the AEA of the OA with Onyx.
TVE: Trans-SSS approach with Onyx
Complete No Good
37 Spiotta et al./201431 72/M Headache Bilateral AEA of the OA Frontal vein to the SSS III TVE: Trans-SSS approach with Onyx Complete No Good
38 Spiotta et al./201431 55/F Headache Bilateral AEA of the OA Frontal vein to the SSS, Basal vein of Rosenthal III TVE: Trans-SSS approach with Onyx Complete No Good
39 Albuquerque et al./201432 NM Asymptomatic Unilateral AEA of the OA Frontal vein to the SSS III TVE: Trans-SSS approach with coils. Complete No Good
40 Deng et al./201414 NM Headache Bilateral AEA of the OA, Unilateral MMA and ethmoidal branches of the IMA Frontal vein to the SSS, Basal vein of Rosenthal IV TAE: via the MMA to embolize the DAVF with Onyx. Complete No IM
41 Deng et al./201414 NM SAH Bilateral AEA of the OA, Unilateral MMA Frontal vein to the SSS IV TAE: via the MMA to embolize the DAVF with Onyx. Complete No Good
42 Inoue et al./201433 58/M Exophthalmos, chemosis and diplopia Bilateral AEA of the OA Superior and inferior ophthalmic veins III TAE: via both AEAs of the OAs with NBCA Complete No Good
43 Cannizzaro et al./201834 80/M Headache Unilateral AEA of the OA, ethmoidal branches of the IMA and MMA Frontal vein to the SSS IV TAE: via the MMA to embolize the DAVF with Onyx. Complete No Good
44 Limbucci et al./201835 59/F Headache Bilateral AEA of the OA Frontal vein to the SSS III TVE: Trans-SSS approach with coils. Complete No Good
45 Limbucci et al./201835 63/F Asymptomatic Bilateral AEA of the OA Frontal vein to the SSS III TVE: Trans-SSS approach with Onyx Complete No Good
46 Limbucci et al./201835 50/M Asymptomatic Bilateral AEA of the OA Frontal vein to the SSS III TVE: Trans-SSS approach with Onyx Complete No Good
47 Limbucci et al./201835 70/M IH Bilateral AEA of the OA, ethmoidal branches of the IMA Basal vein of Rosenthal IV TVE: Trans-Basal vein of Rosenthal approach with Onyx Complete No Good
48 Sirakov et al./201836 40/M SDH Bilateral AEA of the OA Frontal vein to the SSS IV TAE: via the AEA of the OA with Onyx. Complete No Good

Abbreviations: EVT: endovascular treatment; ACF: anterior cranial fossa; DAVF: dural arteriovenous fistula; M: male; IH: Intracerebral hematoma; AEA: anterior ethmoidal artery; OA: ophthalmic artery; SSS: superior sagittal sinus; TAE: transarterial embolization; NBCA: N-butyl-2-cyanoacrylate; SAH: subarachnoid hemorrhage; IMA: Internal maxillary artery; TVE: transvenous embolization; MMA: middle meningeal artery; ACA: anterior cerebral artery; MCA: middle cerebral artery; PEA: posterior ethmoidal artery; F: female; IM: improved; SDH: subdural hematoma; IVH: intraventricular hemorrhage; NM: not mentioned

Table 2.

General and angiographic data in ACF DAVF series

No. Author/Year Cases Mean Age (years) Male Sex Hemorrhagic presentation Arterial feeders Venous drainage
1 Başkaya et al./19946 50 cases 56 81% 77% AEA of the OA: 100%. Frontal vein into the SSS: 75%.
2 Lawton et al./199938 16 cases 62 68% 50% AEA of the OA: 100% (50% were bilateral).
Ethmoidal branch of the IMA: 31%.
Frontal vein into the SSS: 62.5%.
Cavernous sinus: 44.8%.
Basal vein of Rosenthal: 2.5%.
Labbé vein: 2.5%.
Venous ectasia: 69%.
3 Agid et al./20099 24 cases 57 92% 46% AEA of the OA: 100% (all were bilateral).
Ethmoidal branch of the IMA and MMA: 62%.
Frontal vein into the SSS: 75%.
Superficial sylvian veins: 21%.
Basal vein of Rosenthal: 4%.
Venous ectasia: 46%.
4 Li et al./201312 11 cases 50 91% 82% AEA of the OA: 100% (all bilateral).
Ethmoidal branch of the IMA: 36%.
MMA: 27%.
Pial branch of the ACA: 18%.
Branches of the facial artery: 18%.
Flow-related aneurysms: 18%.
Frontal vein into the SSS: 100%.
Venous ectasia: 73%.
Cavernous sinus and Basal vein of Rosenthal: 18%.
5 Gross et al./20164 27 cases 62 67% 37% AEA of the OA: 93% (all bilateral).
Ethmoidal branch of the IMA: 66% (bilateral in 48%).
MMA: 22%.
Dural branch of ICA: 7%.
Pial branch of the ACA: 7%.
Flow-related aneurysms: 7%.
Frontal vein into the SSS: 70%.
Basal vein of Rosenthal: 19%.
Superficial sylvian veins and Trolard or Labbé veins: 11%.
Venous ectasia: 59%.
6 Robert et al./201637 10 cases 59 67% 20% AEA of the OA: 100% (80% were bilateral).
Ethmoidal branch of the IMA: 20%.
MMA: 30%.
Frontal vein into the SSS: 60%.
Cavernous sinus: 20%.
Superficial sylvian veins: 20%.
Venous ectasia: 70%.

Abbreviations: ACF: anterior cranial fossa; DAVF: dural arteriovenous fistula; AEA: anterior ethmoidal artery; OA: ophthalmic artery; SSS: superior sagittal sinus; IMA: internal maxillary artery; MMA: Middle meningeal artery; ACA: anterior cerebral artery; ICA internal carotid artery

Material and methods

This systematic review was conducted in accordance with the Preferred Reporting Items for Systematic Reviews and Meta-Analyses (PRISMA) guidelines 16. Eligible English language articles (case reports, case series, and studies considering ACF DAVFs treated via EVT) were identified through searches of PubMed published (last search date was October 2018).

The search algorithm used the terms “anterior cranial fossa dural arteriovenous fistula,” “cribriform plate arteriovenous fistula,” “ethmoidal dural arteriovenous fistula” and “embolization” as key words in relevant combinations. The reference lists of the identified articles were also manually searched for additional studies. The resulting flowchart is depicted in Figure 1.

Figure 1.

Figure 1

Flow chart of the search strategies.

The inclusion criteria were as follows: a) full text was available, b) clinical data were largely complete, and c) EVT was the only treatment used. Patients from EVT studies without sufficient descriptions of the individual demographic, clinical, and radiological data were excluded.

Results

General demographic, clinical, and radiological characteristics

Twenty-four studies 9, 11, 12, 14, 17-36 were identified in the literature search, reporting on a total of 48 patients who met the inclusion criteria. Of these patients, 39 had definite age and sex information, 33 (84.6%, 33/39) were male, and 6 (15.4%, 6/39) were female. The affected patients ranged in age from 37 to 80 years (mean 55.6). Of these 48 patients, 28 (58.3%, 28/48) primarily presented with intracranial hemorrhage (including intracerebral hematoma, subarachnoid hemorrhage, subdural hematoma and intraventricular hemorrhage).

Among the 48 patients, 47 (97.9%, 47/48) had feeding arteries from the anterior ethmoidal artery (AEA) of the ophthalmic artery (OA), 10 (20.8%, 10/48) patients had feeding arteries from the middle meningeal artery (MMA), 16 (33.3%, 16/48) patients had feeding arteries from the ethmoidal branches of internal maxillary artery (IMA), and one (2.1%, 1/48) had feeding arteries from the posterior ethmoidal artery (PEA) of the OA. Among the 48 patients, 40 (83.3%, 40/48) had bilateral feeding arteries, with the remaining 8 (16.7%, 8/48) having unilateral feeding arteries. All 48 cases were high-grade according to the Cognard classification (III-IV) system. Of the 48 patients, 43 (89.6%, 43/48) had drainage into the superior sagittal sinus (SSS), and 8 (16.7%, 8/48) patients had drainage via the Basal vein of Rosenthal.

Treatment process

Of the 48 patients, 36 (75%, 36/48) were treated via TAE. Of these 36 patients, 28 (77.8%, 28/36) were managed via the AEA of the OA, and 6 (16.7%, 6/36) were managed via the middle meningeal artery (MMA).

Of the 48 patients, 12 (25%, 12/48) patients were treated via TVE, and 11 (91.7%, 11/12) were treated via the trans-SSS approach. Of the 12 patients treated via TVE, 2 (16.7%, 2/12) had previously undergone TAE.

Outcome and follow-up

Of the 48 patients, all treated via TAE, complete angiographic cure was achieved in 44 (91.7%, 44/48), while 4 (8.3%, 4/48) patients experienced incomplete angiographic cure. Four (8.3%, 4/48) patients suffered complications, of whom 1 (2.1%, 1/48) exhibited edema of the thalamus and midbrain, 2 (4.2%, 2/47) exhibited excessive Onyx reflux, and 1 (2.1%, 1/48) experienced microcatheter retention. The clinical data are summarized in Table 1. All 48 patients had definite descriptions of follow-up outcomes. In total, 45 (93.8%, 45/48) patients had good outcomes, 2 (4.2%, 2/48) had improved neurological state, and 1 (2.1%, 1/48) was worse than before operation.

Discussion

Angioarchitecture and grade

In ACF DAVFs, the sources of the main feeding arteries are the AEA of the OA and are primarily bilateral4, 5, 8, 9, 11, 24, 31, 37. In the considered ACF DAVF studies (Table 2), the involvement of the AEA of the OA was 93-100%, and 50-100% of ACF DAVFs had bilateral feeding arteries 4, 6, 9, 12, 37, 38. In the identified 48 cases, 97.9% of patients had feeding arteries from the AEA of the OA, and 83.3% of patients had bilateral feeding arteries.

The MMA can be involved in ACF DAVFs and, when involved, is typically unilateral 14, 15, 37. In the considered ACF DAVF studies (Table 2), the rate of MMA involvement was 20-30% 4, 6, 9, 12, 37, 38. In the 48 analyzed cases, the overall rate was 20.8%. The ethmoidal branch (sphenopalatine artery) of the internal maxillary artery (IMA) was also involved in ACF DAVFs. In the studies considered in this series (Table 2), the rate of involvement of the ethmoidal branch of the IMA was 20-66% 4, 6, 9, 12, 37, 38. In the 48 cases, the overall rate was 33.3% 8, 11, 12, 23, 28, 30.

In addition, the pial branches of the ACA and MCA, the angular branch of the facial artery and even the persistent primitive olfactory artery can be involved in ACF DAVFs in rare cases 4, 9, 12, 25, 27, 39, 40. Flow-related aneurysms can occur in the feeding artery in 18% of cases 12.

The fistula point of an ACF DAVF is usually located at the level of the cribriform plate in the lateral epidural space, which includes the lamina cribrosa and the orbital roofs. The fistula point of an ACF DAVF is most often single and located on one side of the cribriform plate 11. Rarely, an ACF DAVF can occur bilaterally 41, 42.

The venous drainage routes of ACF DAVFs include drainage to the frontal veins and then secondarily into the SSS, via the olfactory vein to the cavernous sinus or the basal vein of Rosenthal, or to the sylvian veins and then ultimately into the vein of Trolard or Labbé 8, 11, 12, 15, 24, 28, 38, 43, 44. These venous drainage routes are usually unilateral but can be bilateral in rare cases 40.

Of all such venous drainage routes, the frontal cortical veins to the SSS are the most frequently affected 8, 9, 12. In the considered ACF DAVF studies (Table 2), the rate of drainage into the SSS was 60-100% 4, 6, 9, 12, 37, 38. In the 48 cases, the overall rate was 89.6%.

In addition, Gross et al. reported that in 19% of all cases, ACF DAVFs had venous drainage that was routed posteriorly into the basal vein of Rosenthal and then into the deep venous circulation, sometimes including the lateral mesencephalic vein 4, 11. In the 48 analyzed cases, 16.7% of patients had drainage via Basal vein of Rosenthal. This drainage pattern could be related to hemorrhages that occur at a position remote from the DAVF site 10, 28, 30.

Because the ACF contains no dural sinuses, ACF DAVFs always drain via the cortical venous drainage system. In approximately one-half of ACF DAVFs, hemodynamic stress causes fragile draining veins to undergo progressive structural modifications, including dilation and the formation of a venous aneurysm 8-12, 40, 45-49. Hence, when using the Cognard classification system, ACF DAVFs are often graded as Cognard Type III/IV 10, 12, 24, 37, 50-52. The 48 cases we considered all had high-grade (III-IV) Cognard classifications.

Cognard et al. noted that intracranial hemorrhage was observed in 10% of patients with type II, 40% with type III and 65% with type IV DAVFs 51. In the assessed ACF DAVF studies (Table 2), the rate of intracranial hemorrhage was 22-82% 4, 6, 9, 12, 37, 38. In the 48 cases, the overall rate of intracranial hemorrhage was 58.3%.

Outline of EVT

The therapeutic goal of EVT is for the embolic agents to penetrate through the transosseous shunt to obliterate the fistula point 4, 12. Performing TAE through the OA is considered technically challenging because the surgeon must avoid occluding the central retinal artery (CRA) 17, 30. TVE can achieve complete obliteration, but the route from the puncture point to the DAVF is long and difficult to navigate, especially when passing the venous varix, and TVE is more time consuming and therefore requires more patience 10.

In ACF DAVFs, EVT should be considered only in patients with favorable angiographic anatomy. However, in appropriate patients, EVT is effective and associated with a high obliteration rate 14. TAE is the first option in cases with good transarterial access to the fistulous point (e.g., via a large and easily navigable OA with limited proximal vessel tortuosity) that allows distal microcatheterization to be performed in close proximity to the fistulous point and a tolerable degree of reflux 14, 17, 30. Additionally, due to safety issues, TVE is preferred if the ACF DAVF has an easily navigable draining vein and covers a short cortical distance 10, 37.

Transarterial embolization

When performing TAE for ACF DAVFs, almost all feeding arteries can be used as the TAE path 24, 30. However, TAE is rarely performed when the feeding arteries are too thin, such as when the ethmoidal branch of the IMA is involved 11, 38. Currently, TAE is primarily performed via the OA and MMA, although in rare cases, the facial artery can be used 27.

(i) AEA of OA

In ACF DAVFs, the AEA of the OA is the most frequently reported feeding artery, and in these cases, TAE must be performed via these arteries 12, 53. In the 48 studied cases, 36 patients were treated via TAE. Of these 36 patients, 28 (77.8%, 28/36) were managed via the AEA of the OA. When using TAE to treat an ACF DAVF via the OA, the CRA must be given sufficient consideration during Onyx injection to reduce the risk of retinal ischemia and acute vision loss. Because the space available for Onyx reflux is limited in these patients, excessive reflux should be strictly controlled 9, 30.

The origin of the CRA is at the same level of the ciliary arteries and originates from the second segment of the OA 54. Therefore, the surgeon should ensure that the ciliary arteries are recognized. Moreover, it is essential that there is no evidence of retinal choroidal blush on superselective angiography before the Onyx injection is performed 30. Therefore, the optimal position of the microcatheter is as close as possible to the fistula, and the microcatheter should be placed in the third segment of the OA immediately proximal to the origin of the AEA. Finally, when injecting Onyx, the origin of the CRV should also be noted and kept under consideration 37, 55.

(ii) MMA

In ACF DAVFs, the MMA is usually not the main feeding artery, and its route to the DAVF is very long and occasionally tortuous. For this reason, the MMA is not often used for TAE 14, 15. However, the MMA is actually an excellent path to take when performing TAE because it is strongly resistant to rupturing when the microcatheter is pulled back. Moreover, this vessel contains sufficient space for Onyx reflux, increasing the forward penetration of the Onyx into vascular networks, including nearby drainage veins or feeders 15, 56, 57. Occasionally, a dual lumen balloon and the pressure-cooker technique can help to increase the penetration of the Onyx 37. In our summarized 48 cases, 36 were treated via TAE. Of these 36 patients, 6 (16.7%, 6/36) were managed via the MMA.

However, most ACF DAVFs are primarily supplied by the ethmoidal artery, and in these cases, the OA must be used 12.

Transvenous embolization

In ACF DAVFs, the main advantage of TVE over TAE is that TVE is not associated with a risk of occluding the CRA because the Onyx is deployed directly into the vein 4, 10. In TVE, the trans-SSS approach is widely used. In the 48 cases considered herein, 12 (25%, 12/48) patients were treated via TVE, and 11 (91.7%, 11/12) were treated with the trans-SSS approach. The TVE approach via deep veins is considered to be dangerous.

However, when TVE is used in ACF DAVFs, venous retrograde catheterization becomes difficult because the transvenous routes are tortuous 11, 58. To overcome this difficulty, it is recommended that TVE be performed via a puncture of the internal jugular vein 10, 11. In addition, it can be helpful to use a flexible intracranial guiding catheter or an intermediate catheter that is advanced to the ostium of the cortical draining vein 10, 31.

When TVE is performed in an ACF DAVF, after the microcatheter tip is positioned in the fistula point, arteriography of the OA and superselective venography of the microcatheter are necessary to confirm the placement of the microcatheter tip 11, 31. When performing TVE, Onyx is a good choice because it can penetrate the fistula through the cribriform plate and can pass retrogradely into the tiny transosseous arterial feeders 59. In the 48 cases we considered, we found that Onyx has become popular in EVT for ACF DAVFs since 2005.

Complications

In EVT for ACF DAVFs, the overall complication rate is 6.25% 4. In the 48 cases considered in this review, the rate of postprocedure complications was 8.3%. Of all complications, CRA ischemia is the most dangerous and damaging complication associated with TAE and is caused by Onyx excessive reflux into the OA 37. In our paper, 2 (4.2%, 2/47) patients experienced excessive Onyx reflux. Thus, when retrograde Onyx approaches the origin of the CRA, low molecular-weight heparin should be postoperatively administered every 12 h for the first 72 h, and 100 mg aspirin should be administered per day for the first month to prevent ischemic events in the CRA 12.

Microcatheter retention can occur when using an undetachable microcatheter. In addition, while injecting Onyx via a feeding artery in TAE, the Onyx may reflux into the contralateral ethmoidal branches and then into the OA. Therefore, the inappropriate migration of Onyx to the contralateral side must be closely monitored during injection 60.

When performing TVE in a patient with tortuous vein anatomy, vein navigation may cause venous perforation, resulting in intracranial hemorrhage. Alternatively, the microcatheter can become embedded in the veins. Hence, excessively tortuous vein anatomy is a contraindication for TVE 30. Rarely, if the EVT disturbs the drainage of the deep vein system, congestion in the BVR is likely to result in transient thalamic and brainstem edema.

Prognosis

After appropriate patients are selected, EVT, including TAE and TVE, achieve good therapeutic outcomes 10, 12, 15, 28, 30. From a statistical standpoint, TAE has an occlusion rate ranging from 12.5% to 63.6% in ACF DAVFs 4, 9, whereas TVE has achieved a complete occlusion rate of 63.3-91% in a larger series 8. Completely occluding the ACF DAVF is associated with good outcomes. In the 48 cases considered herein, 91.7% of patients experienced complete angiographic cure, and 93.8% of patients had a good outcome.

Summary

The fistula point of an ACF DAVF is usually located at the level of the cribriform plate, and the AEA of the OA was the most commonly observed feeding artery. The frontal cortical veins to the SSS are the most frequently involved. Because of their cortical vein drainage pattern, ACF DAVFs often have a malignant natural history with high-grade Cognard classifications (III-IV). EVT, including TAE and TVE, is currently considered an effective therapeutic option in ACF DAVFs. The therapeutic goal of EVT is for the embolic agents to penetrate through the transosseous shunt to obliterate the fistula point.

When performing TAE through the AEA of the OA, it is important to ensure that the CRA is not occluded. TVE can also achieve complete obliteration, but the path from the puncture point to the DAVF is longer and difficult to navigate, meaning that TVE is more time consuming and requires more patience. EVT is associated with both technique- and treatment-related complications. However, although complications may occur, AVF DAVFs have an acceptable prognosis when the patients are appropriately selected.

Limitations

ACF DAVFs are rare intracranial lesions, most of which are sporadically presented as case reports. As a result of the small sample size in this review, the statistical analysis is inappropriate. Because of the selection criteria in this study, cases without adequate description of the patients' medical histories were excluded. Cases mixed in with larger case series with DAVFs of other intracranial locations were also occasionally omitted due to the difficulty of data extraction. Furthermore, only articles written in English were included in this study. Hence, the findings of this review may not reflect actual circumstances in the clinic, and readers should interpret the presented results with the appropriate level of caution.

References

  • 1.Guo Y, Yu J, Zhao Y, Yu J. Progress in research on intracranial multiple dural arteriovenous fistulas. Biomed Rep. 2018;8:17–25. doi: 10.3892/br.2017.1021. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 2.Yu J, Lv X, Li Y, Wu Z. Therapeutic progress in pediatric intracranial dural arteriovenous shunts: A review. Interv Neuroradiol. 2016;22:548–56. doi: 10.1177/1591019916653254. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 3.Ishikawa T, Houkin K, Tokuda K, Kawaguchi S, Kashiwaba T. Development of anterior cranial fossa dural arteriovenous malformation following head trauma. Case report. J Neurosurg. 1997;86:291–3. doi: 10.3171/jns.1997.86.2.0291. [DOI] [PubMed] [Google Scholar]
  • 4.Gross BA, Moon K, Kalani MY, Albuquerque FC, McDougall CG, Nakaji P. et al. Clinical and Anatomic Insights From a Series of Ethmoidal Dural Arteriovenous Fistulas at Barrow Neurological Institute. World Neurosurg. 2016;93:94–9. doi: 10.1016/j.wneu.2016.05.052. [DOI] [PubMed] [Google Scholar]
  • 5.Hattori T, Kobayashi H, Inoue S, Sakai N. Angiographically occult dural arteriovenous malformation in the anterior cranial fossa-case report. Neurol Med Chir (Tokyo) 1999;39:291–3. doi: 10.2176/nmc.39.291. [DOI] [PubMed] [Google Scholar]
  • 6.Baskaya MK, Suzuki Y, Seki Y, Negoro M, Ahmed M, Sugita K. Dural arteriovenous malformations in the anterior cranial fossa. Acta Neurochir (Wien) 1994;129:146–51. doi: 10.1007/BF01406494. [DOI] [PubMed] [Google Scholar]
  • 7.Tsai LK, Liu HM, Jeng JS. Diagnosis and management of intracranial dural arteriovenous fistulas. Expert Rev Neurother. 2016;16:307–18. doi: 10.1586/14737175.2016.1149063. [DOI] [PubMed] [Google Scholar]
  • 8.Meneghelli P, Pasqualin A, Lanterna LA, Bernucci C, Spinelli R, Dorelli G. et al. Surgical treatment of anterior cranial fossa dural arterio-venous fistulas (DAVFs): a two-centre experience. Acta Neurochir (Wien) 2017;159:823–30. doi: 10.1007/s00701-017-3107-2. [DOI] [PubMed] [Google Scholar]
  • 9.Agid R, Terbrugge K, Rodesch G, Andersson T, Soderman M. Management strategies for anterior cranial fossa (ethmoidal) dural arteriovenous fistulas with an emphasis on endovascular treatment. J Neurosurg. 2009;110:79–84. doi: 10.3171/2008.6.17601. [DOI] [PubMed] [Google Scholar]
  • 10.Limbucci N, Leone G, Nappini S, Rosi A, Renieri L, Consoli A, Transvenous Embolization of Ethmoidal Dural Arteriovenous Fistulas: Case Series and Review of the Literature. World Neurosurg; 2017. [DOI] [PubMed] [Google Scholar]
  • 11.Defreyne L, Vanlangenhove P, Vandekerckhove T, Deschrijver I, Sieben G, Klaes R. et al. Transvenous embolization of a dural arteriovenous fistula of the anterior cranial fossa: preliminary results. AJNR Am J Neuroradiol. 2000;21:761–5. [PMC free article] [PubMed] [Google Scholar]
  • 12.Li Q, Fang YB, Huang QH, Zhang Q, Hong B, Zhao WY. et al. Transarterial embolization of dural arteriovenous fistulas of the anterior cranial fossa with Onyx. J Clin Neurosci. 2013;20:287–91. doi: 10.1016/j.jocn.2012.03.031. [DOI] [PubMed] [Google Scholar]
  • 13.Kortman HG, Bloemsma G, Boukrab I, Peluso JP, Sluzewski M, van der Pol B. et al. Treatment of cranial dural arteriovenous fistulas with exclusive cortical venous drainage: A single-center cohort of 35 patients. Interv Neuroradiol. 2017;23:661–5. doi: 10.1177/1591019917728399. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 14.Deng JP, Li J, Zhang T, Yu J, Zhao ZW, Gao GD. Embolization of dural arteriovenous fistula of the anterior cranial fossa through the middle meningeal artery with Onyx. Clin Neurol Neurosurg. 2014;117:1–5. doi: 10.1016/j.clineuro.2013.11.013. [DOI] [PubMed] [Google Scholar]
  • 15.Cannizzaro D, Peschillo S, Cenzato M, Pero G, Resta MC, Guidetti G, Endovascular and surgical approaches of ethmoidal dural fistulas: a multicenter experience and a literature review. Neurosurg Rev; 2016. [DOI] [PubMed] [Google Scholar]
  • 16.Liberati A, Altman DG, Tetzlaff J, Mulrow C, Gotzsche PC, Ioannidis JP. et al. The PRISMA statement for reporting systematic reviews and meta-analyses of studies that evaluate healthcare interventions: explanation and elaboration. BMJ. 2009;339:b2700. doi: 10.1136/bmj.b2700. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 17.Matsumaru Y, Alvarez H, Rodesch G, Lasjaunias PL. Embolisation of branches of the ophthalmic artery. Interv Neuroradiol. 1997;3:239–45. doi: 10.1177/159101999700300306. [DOI] [PubMed] [Google Scholar]
  • 18.Abrahams JM, Bagley LJ, Flamm ES, Hurst RW, Sinson GP. Alternative management considerations for ethmoidal dural arteriovenous fistulas. Surg Neurol. 2002;58:410–6. doi: 10.1016/s0090-3019(02)00871-6. discussion 6. [DOI] [PubMed] [Google Scholar]
  • 19.Flynn TH, McSweeney S, O'Connor G, Kaar G, Ryder DQ. Dural AVM supplied by the ophthalmic artery. Br J Neurosurg. 2007;21:414–6. doi: 10.1080/02688690701411590. [DOI] [PubMed] [Google Scholar]
  • 20.Xianli L, Youxiang L, Aihua L, Ming L, Zhongxue W. Transarterial embolization of dural arteriovenous fistulas of the anterior cranial fossa using onyx-18. A case report. Neuroradiol J. 2007;20:348–54. doi: 10.1177/197140090702000318. [DOI] [PubMed] [Google Scholar]
  • 21.Katsaridis V, Papagiannaki C, Violaris C. Endovascular treatment of a bilateral ophthalmic-ethmoidal artery dural arteriovenous fistula. J Neuroophthalmol. 2007;27:281–4. doi: 10.1097/WNO.0b013e31815b99ee. [DOI] [PubMed] [Google Scholar]
  • 22.Lv X, Jiang C, Li Y, Yang X, Wu Z. Percutaneous Transvenous Embolization of Intracranial Dural Arteriovenous Fistulas with Detachable Coils and/or in Combination with Onyx. Interv Neuroradiol. 2008;14:415–27. doi: 10.1177/159101990801400407. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 23.Lv X, Li Y, Wu Z. Endovascular treatment of anterior cranial fossa dural arteriovenous fistula. Neuroradiology. 2008;50:433–7. doi: 10.1007/s00234-007-0346-6. [DOI] [PubMed] [Google Scholar]
  • 24.Tahon F, Salkine F, Amsalem Y, Aguettaz P, Lamy B, Turjman F. Dural arteriovenous fistula of the anterior fossa treated with the Onyx liquid embolic system and the Sonic microcatheter. Neuroradiology. 2008;50:429–32. doi: 10.1007/s00234-007-0344-8. [DOI] [PubMed] [Google Scholar]
  • 25.Tsutsumi S, Shimizu Y, Nonaka Y, Abe Y, Yasumoto Y, Ito M. et al. Arteriovenous fistula arising from the persistent primitive olfactory artery with dual supply from the bilateral anterior ethmoidal arteries. Neurol Med Chir (Tokyo) 2009;49:407–9. doi: 10.2176/nmc.49.407. [DOI] [PubMed] [Google Scholar]
  • 26.Guedin P, Gaillard S, Boulin A, Condette-Auliac S, Bourdain F, Guieu S. et al. Therapeutic management of intracranial dural arteriovenous shunts with leptomeningeal venous drainage: report of 53 consecutive patients with emphasis on transarterial embolization with acrylic glue. J Neurosurg. 2010;112:603–10. doi: 10.3171/2009.7.JNS08490. [DOI] [PubMed] [Google Scholar]
  • 27.Ishihara H, Ishihara S, Neki H, Okawara M, Kanazawa R, Kohyama S. et al. Dural arteriovenous fistula of the anterior cranial fossa with carotid artery stenosis treated by simultaneous transarterial embolization and carotid artery stenting. Neurol Med Chir (Tokyo) 2010;50:995–7. doi: 10.2176/nmc.50.995. [DOI] [PubMed] [Google Scholar]
  • 28.Mack WJ, Gonzalez NR, Jahan R, Vinuela F. Endovascular management of anterior cranial fossa dural arteriovenous malformations. A technical report and anatomical discussion. Interv Neuroradiol. 2011;17:93–103. doi: 10.1177/159101991101700115. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 29.Zhao WY, Krings T, Yang PF, Liu JM, Xu Y, Li Q. et al. Balloon-assisted superselective microcatheterization for transarterial treatment of cranial dural arteriovenous fistulas: technique and results. Neurosurgery. 2012;71:ons269–73. doi: 10.1227/NEU.0b013e3182684b70. discussion ons73. [DOI] [PubMed] [Google Scholar]
  • 30.Li C, Wu Z, Yang X, Li Y, Jiang C, He H. Transarterial treatment with Onyx of Cognard type IV anterior cranial fossa dural arteriovenous fistulas. J Neurointerv Surg. 2014;6:115–20. doi: 10.1136/neurintsurg-2012-010641. [DOI] [PubMed] [Google Scholar]
  • 31.Spiotta AM, Hawk H, Kellogg RT, Turner RD, Chaudry MI, Turk AS. Transfemoral venous approach for Onyx embolization of anterior fossa dural arteriovenous fistulae. J Neurointerv Surg. 2014;6:195–9. doi: 10.1136/neurintsurg-2012-010642. [DOI] [PubMed] [Google Scholar]
  • 32.Albuquerque FC, Ducruet AF, Crowley RW, Bristol RE, Ahmed A, McDougall CG. Transvenous to arterial Onyx embolization. J Neurointerv Surg. 2014;6:281–5. doi: 10.1136/neurintsurg-2012-010628. [DOI] [PubMed] [Google Scholar]
  • 33.Inoue A, Tagawa M, Kumon Y, Watanabe H, Shoda D, Sugiu K. et al. Ethmoidal dural arteriovenous fistula with unusual drainage route treated by transarterial embolization. J Neurointerv Surg. 2015;7:e15. doi: 10.1136/neurintsurg-2013-011098.rep. [DOI] [PubMed] [Google Scholar]
  • 34.Cannizzaro D, Peschillo S, Cenzato M, Pero G, Resta MC, Guidetti G. et al. Endovascular and surgical approaches of ethmoidal dural fistulas: a multicenter experience and a literature review. Neurosurg Rev. 2018;41:391–8. doi: 10.1007/s10143-016-0764-1. [DOI] [PubMed] [Google Scholar]
  • 35.Limbucci N, Leone G, Nappini S, Rosi A, Renieri L, Consoli A. et al. Transvenous Embolization of Ethmoidal Dural Arteriovenous Fistulas: Case Series and Review of the Literature. World Neurosurg. 2018;110:e786–e93. doi: 10.1016/j.wneu.2017.11.095. [DOI] [PubMed] [Google Scholar]
  • 36.Sirakov S, Sirakov A, Hristov H, Ninov K. Successful endovascular treatment of ruptured bilateral ophthalmic frontal dural arteriovenous fistula. Radiol Case Rep. 2018;13:1036–41. doi: 10.1016/j.radcr.2018.04.011. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 37.Robert T, Blanc R, Smajda S, Ciccio G, Redjem H, Bartolini B. et al. Endovascular treatment of cribriform plate dural arteriovenous fistulas: technical difficulties and complications avoidance. J Neurointerv Surg. 2016;8:954–8. doi: 10.1136/neurintsurg-2015-011956. [DOI] [PubMed] [Google Scholar]
  • 38.Lawton MT, Chun J, Wilson CB, Halbach VV. Ethmoidal dural arteriovenous fistulae: an assessment of surgical and endovascular management. Neurosurgery. 1999;45:805–10. doi: 10.1097/00006123-199910000-00014. discussion 10-1. [DOI] [PubMed] [Google Scholar]
  • 39.Ros de San Pedro J, Perez CJ, Parra JZ, Lopez-Guerrero AL, Sanchez JF. Bilateral ethmoidal dural arteriovenous fistula: unexpected surgical diagnosis. Clin Neurol Neurosurg. 2010;112:903–8. doi: 10.1016/j.clineuro.2010.07.006. [DOI] [PubMed] [Google Scholar]
  • 40.Kohama M, Nishimura S, Mino M, Hori E, Yonezawa S, Kaimori M. et al. Anterior cranial fossa dural arteriovenous fistula with bilateral cortical drainers-case report. Neurol Med Chir (Tokyo) 2010;50:217–20. doi: 10.2176/nmc.50.217. [DOI] [PubMed] [Google Scholar]
  • 41.Deshmukh VR, Chang S, Albuquerque FC, McDougall CG, Spetzler RF. Bilateral ethmoidal dural arteriovenous fistulae: a previously unreported entity: case report. Neurosurgery. 2005;57:E809. doi: 10.1093/neurosurgery/57.4.e809. [DOI] [PubMed] [Google Scholar]
  • 42.Yurekli VA, Orhan G, Gurkas E, Senol N. Bilateral ophthalmic-ethmoidal dural arteriovenous fistula presenting with intracranial hemorrhage: a rare entity. Neurol Sci. 2013;34:1851–3. doi: 10.1007/s10072-013-1331-y. [DOI] [PubMed] [Google Scholar]
  • 43.Kiyosue H, Hori Y, Okahara M, Tanoue S, Sagara Y, Matsumoto S. et al. Treatment of intracranial dural arteriovenous fistulas: current strategies based on location and hemodynamics, and alternative techniques of transcatheter embolization. Radiographics. 2004;24:1637–53. doi: 10.1148/rg.246045026. [DOI] [PubMed] [Google Scholar]
  • 44.Tanei T, Fukui K, Wakabayashi K, Mitsui Y, Inoue N, Watanabe M. Dural arteriovenous fistula in the anterior cranial fossa: four case reports. Neurol Med Chir (Tokyo) 2008;48:560–3. doi: 10.2176/nmc.48.560. [DOI] [PubMed] [Google Scholar]
  • 45.Ding D, Starke RM, Crowley RW, Liu KC. Interhemispheric approach for endoscopic ligation of an anterior cranial fossa dural arteriovenous fistula. J Clin Neurosci. 2015;22:1969–72. doi: 10.1016/j.jocn.2015.06.003. [DOI] [PubMed] [Google Scholar]
  • 46.Sato K, Shimizu T, Fukuhara T, Namba Y. Ruptured anterior communicating artery aneurysm associated with anterior cranial fossa dural arteriovenous fistula-case report. Neurol Med Chir (Tokyo) 2011;51:40–4. doi: 10.2176/nmc.51.40. [DOI] [PubMed] [Google Scholar]
  • 47.Chen Z, Tang W, Liu Z, Li F, Feng H, Zhu G. A dural arteriovenous fistula of the anterior cranial fossa angiographically mimicking an anterior ethmoidal artery aneurysm. J Neuroimaging. 2010;20:382–5. doi: 10.1111/j.1552-6569.2009.00392.x. [DOI] [PubMed] [Google Scholar]
  • 48.Hashiguchi A, Mimata C, Ichimura H, Morioka M, Kuratsu J. Venous aneurysm development associated with a dural arteriovenous fistula of the anterior cranial fossa with devastating hemorrhage-case report. Neurol Med Chir (Tokyo) 2007;47:70–3. doi: 10.2176/nmc.47.70. [DOI] [PubMed] [Google Scholar]
  • 49.Ogawa T, Okudera T, Miyauchi T, Inugami A, Uemura K, Yasui N. Anterior cranial fossa dural arteriovenous fistula with a varix mimicking an anterior communicating artery aneurysm. Neuroradiology. 1996;38:252–3. doi: 10.1007/BF00596541. [DOI] [PubMed] [Google Scholar]
  • 50.Gomez J, Amin AG, Gregg L, Gailloud P. Classification schemes of cranial dural arteriovenous fistulas. Neurosurg Clin N Am. 2012;23:55–62. doi: 10.1016/j.nec.2011.09.003. [DOI] [PubMed] [Google Scholar]
  • 51.Cognard C, Gobin YP, Pierot L, Bailly AL, Houdart E, Casasco A. et al. Cerebral dural arteriovenous fistulas: clinical and angiographic correlation with a revised classification of venous drainage. Radiology. 1995;194:671–80. doi: 10.1148/radiology.194.3.7862961. [DOI] [PubMed] [Google Scholar]
  • 52.Borden JA, Wu JK, Shucart WA. A proposed classification for spinal and cranial dural arteriovenous fistulous malformations and implications for treatment. J Neurosurg. 1995;82:166–79. doi: 10.3171/jns.1995.82.2.0166. [DOI] [PubMed] [Google Scholar]
  • 53.Gliemroth J, Nowak G, Arnold H. Dural arteriovenous malformation in the anterior cranial fossa. Clin Neurol Neurosurg. 1999;101:37–43. doi: 10.1016/s0303-8467(98)00075-4. [DOI] [PubMed] [Google Scholar]
  • 54.Tsutsumi S, Rhoton AL Jr. Microsurgical anatomy of the central retinal artery. Neurosurgery. 2006;59:870–8. doi: 10.1227/01.NEU.0000232654.15306.4A. discussion 8-9. [DOI] [PubMed] [Google Scholar]
  • 55.Alvarez H, Rodesch G, Garcia-Monaco R, Lasjaunias P. Embolisation of the ophthalmic artery branches distal to its visual supply. Surg Radiol Anat. 1990;12:293–7. doi: 10.1007/BF01623709. [DOI] [PubMed] [Google Scholar]
  • 56.Griessenauer CJ, He L, Salem M, Chua MH, Ogilvy CS, Thomas AJ. Middle meningeal artery: Gateway for effective transarterial Onyx embolization of dural arteriovenous fistulas. Clin Anat. 2016;29:718–28. doi: 10.1002/ca.22733. [DOI] [PubMed] [Google Scholar]
  • 57.Yu J, Guo Y, Xu B, Xu K. Clinical importance of the middle meningeal artery: A review of the literature. Int J Med Sci. 2016;13:790–9. doi: 10.7150/ijms.16489. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 58.Matsuzaki J, Kono K, Umesaki A, Kashimura Y, Matsumoto H, Terada T. [Transvenous Embolization by Direct Puncture of the Superior Sagittal Sinus Using Indocyanine Green(ICG)Videoangiography for Treatment of Dural Arteriovenous Fistula of the Transverse-Sigmoid Sinus:A Case Report] No Shinkei Geka. 2017;45:591–8. doi: 10.11477/mf.1436203556. [DOI] [PubMed] [Google Scholar]
  • 59.Mendes GA, Caire F, Saleme S, Ponomarjova S, Mounayer C. Retrograde leptomeningeal venous approach for dural arteriovenous fistulas at foramen magnum. Interv Neuroradiol. 2015;21:244–8. doi: 10.1177/1591019915582942. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 60.Jamous MA, Satoh K, Satomi J, Matsubara S, Nakajima N, Uno M. et al. Detection of enlarged cortical vein by magnetic resonance imaging contributes to early diagnosis and better outcome for patients with anterior cranial fossa dural arteriovenous fistula. Neurol Med Chir (Tokyo) 2004;44:516–20. doi: 10.2176/nmc.44.516. discussion 20-1. [DOI] [PubMed] [Google Scholar]

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