- •Foreword
- •Preface
- •Glossary
- •1. Introduction
- •2. Historical Considerations
- •2.1 Arteriovenous Fistula and Pulsating Exophthalmos
- •2.2 Angiography
- •2.3 Therapeutic Measures
- •2.4 Embolization
- •References
- •3.1 Osseous Anatomy
- •3.1.1 Orbit
- •3.2 Anatomy of the Dura Mater and the Cranial Nerves
- •3.2.1 Autonomic Nervous System
- •3.3 Vascular Anatomy
- •3.3.1 Arterial Anatomy
- •3.3.1.1 Internal Carotid Artery
- •Meningohypophyseal Trunk (MHT)
- •Ophthalmic Artery
- •Ethmoidal Arteries
- •3.3.1.2 External Carotid Artery
- •3.3.1.2.1 Ascending Pharyngeal Artery
- •3.3.1.2.2 Internal Maxillary Artery
- •3.3.1.2.3 Middle Meningeal Artery
- •3.3.1.2.4 Accessory Meningeal Artery
- •3.3.2 Venous Anatomy
- •3.3.2.1.1 Embryology
- •3.3.2.1.2 Anatomy and Topography
- •Orbital Veins
- •Superior Ophthalmic Vein
- •Inferior Ophthalmic Vein
- •Central Retinal Vein (No Direct CS Tributary)
- •Uncal Vein, Uncinate Vein
- •Sphenoparietal sinus (Breschet), Sinus alae parvae, Sinus sphenoidales superior (Sir C. Bell)
- •Intercavernous Sinus, Sinus intercavernosus, Sinus circularis (Ridley), Sinus ellipticus, Sinus coronarius, Sinus clinoideus (Sir C. Bell), Sinus transversus sellae equinae (Haller)
- •Meningeal Veins
- •Veins of the Foramen Rotundum, Emissary Vein
- •Inferior Petrosal Sinus, Sinus petrosus profundus, Sinus petro-occipitalis superior (Trolard)
- •Venous Plexus of the Hypoglossal Canal, Anterior Condylar Vein
- •Posterior Condylar Vein
- •Lateral Condylar Vein
- •Inferior Petroclival Vein
- •Petro-occipital Sinus, Sinus petro-occipitalis inferior, petro-occipital vein (Padget)
- •Transverse Occipital Sinus (Doyen)
- •Basilar Plexus (Virchow)
- •Marginal Sinus
- •Foramen Ovale Plexus (Trigeminal Sinus), Sphenoid Emissary, “Rete” of the Foramen Ovale
- •Vein of the Sphenoid Foramen (Foramen Venosum, Foramen of Vesalius)
- •Foramen Lacerum Plexus
- •Pterygoid Plexus
- •3.3.2.4 Other Veins of Importance for the CS Drainage or for Transvenous Access to the CS
- •Facial Vein
- •Frontal Vein
- •Angular Vein
- •Middle Temporal Vein
- •Internal Jugular Vein
- •The External Jugular Vein
- •Vertebral Vein, Vertebral Artery Venous Plexus
- •Deep Cervical Vein
- •References
- •Introduction
- •4.1.1 Dural Arteriovenous Fistulas (DAVFs)
- •4.1.2 Cavernous Sinus Fistulas (CSFs)
- •References
- •Introduction
- •5.1 Etiology and Pathogenesis of Type A Fistulas
- •5.2 Etiology and Pathogenesis of Type B–D Fistulas
- •5.2.1 Pregnancy
- •5.2.2 Hormonal Factors
- •5.2.3 Thrombosis
- •5.2.4 Venous Hypertension
- •5.2.5 Trauma
- •5.2.6 Embolization
- •5.2.7 Congenital
- •5.2.8 Other Potential Factors
- •5.2.9 Various
- •5.3 Prevalence
- •5.3.1 Natural History
- •References
- •Introduction
- •6.1 Extraorbital Ocular Symptoms
- •6.1.1 Orbital Pain
- •6.2 Orbital Symptoms
- •6.2.1 Exophthalmos
- •6.2.2 Conjunctival Engorgement and Chemosis
- •6.2.2.1 Retinal Hemorrhage
- •6.2.3 Corneal Damage
- •6.2.4 Orbital Bruit
- •6.2.6 Secondary Glaucoma and Visual Loss
- •6.3 Other and Neurological Symptoms
- •References
- •7. Radiological Diagnosis of DCSFs
- •7.1 Non-invasive Imaging Techniques
- •7.1.2 Doppler and Carotid Duplex Sonography
- •7.2 Intra-arterial Digital Subtraction Angiography (DSA)
- •7.2.1 Introduction
- •7.2.2 Technique
- •7.2.3 Angiographic Protocol for DCSFs
- •7.2.4 Angiographic Anatomy of the Cavernous Sinus
- •7.2.5 Flat Detector Technology in Neuroangiography
- •7.2.6 Rotational Angiography and 3D-DSA
- •7.2.6.1 Dual Volume Technique (DVT)
- •7.2.6.2 Angiographic Computed Tomography (ACT), DynaCT (Siemens), C-arm Flat Detector CT (FD-CT), Flat Panel CT (FP-CT) or Cone Beam CT
- •7.2.6.3 Image Post-Processing
- •7.2.6.4 3D Studies of the Cavernous Sinus Region
- •References
- •8. Endovascular Treatment
- •8.1 Techniques of Transvenous Catheterization
- •8.1.1 Inferior Petrosal Sinus Approach
- •8.1.2 Alternative Approaches to the Cavernous Sinus
- •8.1.3 Other Techniques
- •8.2 Embolic Agents
- •8.2.1 Polyvinyl Alcohol (PVA) and Embospheres
- •8.2.2 Stainless Steel Coils
- •8.2.5 Stents
- •8.3.1 Approaches (Benndorf et al. 2004)
- •8.3.2 Angiographic and Clinical Outcome
- •8.4 Discussion of Transvenous Occlusions
- •8.4.1 Approaches
- •8.4.1.1 IPS Approaches
- •8.4.1.6 Transfemoral Pterygoid Plexus Approach (PP Approach)
- •8.4.1.7 Transfemoral Cortical Vein Approach
- •8.4.1.10 Direct Puncture of the Foramen Ovale
- •8.4.2 Embolic Materials
- •8.4.2.1 Particles
- •8.4.2.2 Coils
- •HydroCoils (Hydrogel)
- •8.4.2.4 Ethylene-Vinyl Alcohol Copolymer (OnyxTM)
- •8.4.2.5 Stents and Covered Stents
- •8.4.3 Anatomic Results, Clinical Outcome and Complications of Transvenous Occlusions and Transarterial Embolizations
- •8.5 Conclusion
- •References
- •9. Alternative Treatment Options
- •9.1 Spontaneous Thrombosis
- •9.2 Manual Compression Therapy
- •9.4 Radiotherapy
- •9.5 Surgery
- •References
- •10. Hemodynamic Aspects of DCSFs
- •10.1 Introduction
- •10.2 Basic Hemodynamic Principles
- •10.3 Invasive Assessment of Hemodynamics
- •10.4 Flow Velocity and Pressure Measurements in Brain AVMs and DAVFs
- •10.5 Hemodynamics and Pathophysiology in CSFs
- •Comments
- •References
- •11. Summary
- •Subject Index
106 7 |
Radiological Diagnosis of DCSFs |
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Fig. 7.9 a,b. MRA source images in a DCSF pre and post embolization. Contrast enhanced T1-weighted images preand post transvenous occlusion of a bilateral DCSF. The dark areas in b correspond to the bright areas in both CSs in a (asterisks), confirming that platinum coils have been packed in the previously AV shunting compartments. There is no signal abnormality that would indicate a residual shunt, suggesting that MRA could be used for non-invasive FU. Note, however, that a minimal AV shunt can be missed; to rule out a small residual fistula with certainty, intra-arterial DSA remains indispensable. (Courtesy: G. Gal, Odense)
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Fig. 7.10 a,b. Computed tomography in two DCSF patients post embolization. a Post-embolization CT reveals the positioning of the coils within the right CS. b Follow-up CT after a patient presented with transient deficit after TVO. The small hyperdense area in the left frontal lobe (arrow) is likely due to repeated contrast injections during endovascular treatment. Both indications for cross-sectional imaging have become clinical applications for DynaCT (see below)
7.1.2
Doppler and Carotid Duplex Sonography
(Fig. 7.11)
Ultra-sonography represents a cost-effective, noninvasive method for the study of intraorbital hemo-
dynamic parameters in patients with CSFs. However, ultra-sonography is not suitable to visualize the complex venous anatomy of the cavernous sinus, or to rule out cortical or leptomeningeal venous drainage (Belden et al. 1995; Flaharty et al. 1991); therefore, its value for treatment planning is limited.
7.1 Non-invasive Imaging Techniques |
107 |
a
b
c
Fig. 7.11a–c. Color-Doppler ultrasound in a DCSF: Flow reversal in the superior ophthalmic vein.
a A 39 year-old man with dural AV shunt at the posterior CS causing orbital signs on the right
side before embolization. Arteriovenous flow directed towards the probe, depth 4.5 cm. Total flow: 234 ml/min. b Measurement of the inferior ophthalmic vein also
shows arterio-venous shunting flow, directed towards the probe. c Superior ophthalmic vein after successful embolization: Normalization of blood flow direction (Courtesy:
R. de Keizer, Leiden)
108 |
7 Radiological Diagnosis of DCSFs |
In some studies, Doppler sonography has shown value for diagnosis and follow-up in patients with CSF (Belden et al. 1995; Flaharty et al. 1991; Erickson et al. 1989; Munk et al. 1992). It allows for the assessment of direction and velocity of blood flow, as well as the differentiation of a typical venous flow pattern from an arterialized vein with characteristic bi-phasic flow (Erickson et al. 1989).
De Keizer (1986) performed Doppler flow velocity measurements in 35 patients with direct and indirect fistulas (14 traumatic, 21 spontaneous) and found a specific flow pattern in 100% of direct and in 80% of the indirect communications. He recorded his measurements as hematotachograms (HTGs) and found normalization of flow pattern in patients with direct fistulas after embolization. In a more recent article (de Keizer 2003) he points to the difficulty of separating the arterial flow in the supratrochlear artery from the abnormal arterialized flow velocities and pattern in the ophthalmic veins. When the flow velocity in the ICA was additionally found to be abnormal, a direct fistula could be identified in all cases. Color Doppler methods are helpful in differentiating arterial from venous flow. De Keizer also recommends the use of Doppler measurements for monitoring conservative treatment using manual compression.
Lin et al. (1994) suggested the application of duplex carotid sonography (DCS) for hemodynamic classification of CSFs (see Chap. 4) with special emphasis on the resistance index (RI) and the flow volume, based on 14 cases. The authors suggest the use of sonography for screening and follow-up because DCS cannot accurately identify Type B fistulas and is limited in its differentiation between Types C and D fistulas for which angiography remains indispensable. Chiou et al. (1998) were able to verify the complete obliteration of carotid cavernous fistulas in 13 patients (10 posttraumatic and three spontaneous) with color Doppler ultrasonography. The authors found a spiculated waveform with turbulent flow pattern in most of their direct (Type A) fistulas, while patients with indirect fistulas showed a low-resistive arterial pulsatile pattern. In these six patients with DCSFs, radiosurgery was performed and a cure was documented by sonography, a reasonable approach when repeated angiography can be spared. Nevertheless, for final documentation of anatomical cure, angiography was performed. Arning et al. (2006) studied 17 patients with DAVFs and were able to detect AV shunting lesions in 100% if the ECA was examined. In contrast to brain AVMs
that are detectable only in cases with large shunt volume, most DAVFs can be diagnosed because of their supply by ECA branches that lose their characteristic flow pattern as resistance vessels. Assessment of venous drainage pattern, however, is difficult if not impossible and DSA as an initial diagnostic tool remains necessary. Tsai LK et al. (2005) studied a similar series of patients with DAVFs, one group undergoing endovascular treatment and another undergoing only clinical and sonographic follow-up. The authors found a good correlation between the increase of the RI and the effectiveness of the treatment in DAVF located at major sinuses, but not at the CS. This finding was in agreement with a previous study of the same group (Tsai LK et al. 2004) in which the sensitivity of using the ECA-RI was only 54% for cavernous sinus fistulas while it was 86% for non-cavernous sinus AVFs. This discrepancy is likely explained by the relatively small AV shunting volume in most DCSFs thus having rather little impact on the flow in the ECA. Therefore, it appears advisable to combine DCS with Doppler flow imaging of the superior ophthalmic veins (Chen YW et al. 2000). In patients with solely posterior drainage, it might be impossible to depict an abnormal Doppler flow pattern in the SOV, thus leaving angiography as a last resort for a correct diagnosis.
In summary, modern cross-sectional imaging such as CT and MRI provide a correct diagnosis in many cases or can at least raise the suspicion of a CSF. The combination of transcranial and transorbital Doppler sonography and carotid duplex sonography further increases the sensitivity of non-inva- sive imaging. Sonography provides information on blood flow, while CTA and MRI help to delineate the angiomorphology of the arteriovenous communication.
The venous drainage pattern, representing the main morphological feature of a DCSF, causing mainly the clinical symptoms and being often the potential endovascular approach, can often not be imaged to a satisfactory degree. Low-flow fistulas with small or partially thrombosed SOVs may be completely missed. Therefore, not only patients with unclear symptoms, but all patients with DCSFs should eventually undergo an i.a. (intra-arterial) DSA at least once during the course of the disease, regardless of the planned therapeutic management.
