In this article, the authors review general principles and technical details of preoperative embolization of various hypervascular head, neck, and spinal tumors encountered in contemporary neuroendovascular practice. Indications, treatment goals, techniques, outcomes, and complications are discussed, and illustrative case examples are presented.
Key points
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Preoperative endovascular tumor embolization can be used to decrease overall blood loss; to improve visualization at surgery thus facilitating tumor resection; and/or to selectively occlude deep, inaccessible arterial feeders to the tumor.
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Liquid embolic agents (eg, Onyx or NBCA) are the first-line choices for preoperative tumor embolization if distal selective arterial microcatheter access to the tumor is possible; otherwise, particle embolic agents (eg, PVA) can be used.
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Direct tumor puncture with subsequent tumor embolization is an alternative to traditional transarterial embolization for selected tumor types and locations, avoids the need for multiple vessel catheterizations to achieve tumor devascularization, and more reliably achieves intraparenchymal tumor penetration of the liquid embolic agent, which has been suggested but not proven to reduce blood loss at surgery.
Introduction
Endovascular surgery has emerged as an important tool in the treatment of a variety of hypervascular head, neck, and spinal tumors. Although the concept and first use of tumor embolization date back several decades, recent improvements in catheter design, enhanced angiographic imaging capabilities, and the development of novel embolic agents have all combined to make endovascular intervention safer, easier, and thus more commonly used in the management of selected tumors. However, deciding when and how to use endovascular therapy requires careful consideration of multiple patient- and tumor-related factors to achieve the greatest benefit while minimizing the risk of potentially dangerous complications, which may occur during or after embolization. Embolization can be used in select cases as a primary therapy to reduce tumor-related pain, prevent tumor progression, or stop acute tumor-related hemorrhage. This article focuses on preoperative elective tumor embolization, which is used to decrease blood loss and to facilitate surgical resection.
Introduction
Endovascular surgery has emerged as an important tool in the treatment of a variety of hypervascular head, neck, and spinal tumors. Although the concept and first use of tumor embolization date back several decades, recent improvements in catheter design, enhanced angiographic imaging capabilities, and the development of novel embolic agents have all combined to make endovascular intervention safer, easier, and thus more commonly used in the management of selected tumors. However, deciding when and how to use endovascular therapy requires careful consideration of multiple patient- and tumor-related factors to achieve the greatest benefit while minimizing the risk of potentially dangerous complications, which may occur during or after embolization. Embolization can be used in select cases as a primary therapy to reduce tumor-related pain, prevent tumor progression, or stop acute tumor-related hemorrhage. This article focuses on preoperative elective tumor embolization, which is used to decrease blood loss and to facilitate surgical resection.
General principles
Indications
We are increasingly referred patients with a variety of tumors for consideration of preoperative embolization. In such cases, an a priori suspicion exists that the tumor is hypervascular, based on the tumor type, radiographic imaging, or possibly after a biopsy or attempted surgical resection at which time profuse bleeding was encountered. From an anatomic or technical standpoint, if embolization is deemed unfeasible or poses very high risk to a patient, it obviously should not be attempted. However, more commonly, the relevant question is not whether embolization is feasible but rather whether it is necessary. It is important to recognize that tumor hypervascularity alone is not a good reason to subject the patient to the added risk of preoperative embolization, particularly if the tumor is small, the major blood supply to the tumor is superficial or readily accessible early at surgery (as in most meningiomas), and/or if the extra blood loss anticipated without embolization is not excessive and would be physiologically well-tolerated by the patient. However, if substantial blood loss is anticipated without embolization beyond what would be medically acceptable in a given patient harboring a sizable tumor in a difficult surgical location with numerous deep, surgically inaccessible arterial feeders, the appeal of embolization becomes readily apparent. Embolization to devascularize a tumor may also decrease procedural time, which certainly increases convenience to the surgeon, decreases anesthesia time for the patient, and may or may not reduce the total cost of treatment. Overall, the combined risks of embolization and surgery should be less than that of surgery alone to benefit the patient. In any given case, several factors may impact the decision to offer preoperative tumor embolization ( Box 1 ).
Lesion size, location, vascularity, edema
Surgical accessibility of arterial feeders
Endovascular accessibility of arterial feeders
Proximity of important vessels at risk during embolization
Dangerous vascular collaterals and anastomoses
Flow dynamics within lesion
Atherosclerosis, great vessel tortuousity
Medical condition, anesthetic risk
Open surgical plan and associated risk
Embolic Agents
Particle embolic agents
A variety of agents have been used for tumor embolization including silk, gelatin sponge, fibrin glue, and gelatin spheres ( Box 2 ). Particles, such as polyvinyl alcohol (PVA) or Embospheres (Guerbet Biomedical, Louvres, France), may be used to achieve distal tumor penetration when distal, selective feeding artery catheterization is not possible. Smaller particles penetrate more deeply but carry a greater risk of inadvertent embolization of normal adjacent arterial feeders; choosing the particle diameter that maximizes the effectiveness of tumor embolization while minimizing the risk of nontarget embolization of adjacent vessels is an important step and requires experience with these agents. A major disadvantage of the particle embolic agents in current use is that they are radiolucent; therefore, the extent of tumor embolization must be determined indirectly by contrast injection. Furthermore, they have a tendency to dissipate over time, allowing for vessel recanalization before surgical resection if the embolization is performed too far in advance of the planned surgical procedure.
Embolic Agent | Indication |
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Onyx | Intraparenchymal penetration |
NBCA | Distal feeding artery occlusion |
Particle embolics (PVA, Embospheres) | Flow-directed embolization when unable to achieve distal feeding artery access |
Liquid embolic agents
Although particle embolic agents remain widely used at many centers as first-line agents for tumor embolization, the use of liquid embolics, such as n -butyl cyanoacrylate (NBCA; Codman, Raynham, MA) and Onyx (Covidien, Mansfield, MA), has increased significantly in recent years. They allow for excellent tumor capillary bed penetration but require selective feeding artery catheterization with distal microcatheter placement. NBCA is a radiopaque liquid adhesive glue that polymerizes rapidly on contact with ionic substances, such as blood, and can be injected to achieve permanent vessel occlusion. NBCA can be mixed with varying amounts of Ethiodol to modify the rate at which it polymerizes and to customize the injection flow rate and depth during embolization, which is truly “more art than science.” In general, however, NBCA injections must be performed rapidly and continuously and the microcatheter removed in a timely fashion. As injection time increases beyond a relatively short time window, the risk of microcatheter adherence to the glue cast or to the adjacent vessel walls increases, potentially resulting in catheter retention or vessel avulsion.
Onyx, an ethylene vinyl copolymer mixed with dimethyl sulfoxide (DMSO), is a cohesive liquid agent that gradually precipitates in a centripetal fashion after injection as the DMSO diffuses away on contact with blood. Depending on the flow dynamics within the tumor vasculature, lower (Onyx-18) or higher (Onyx-34) viscosity Onyx formulations can be selected for use during embolization. Onyx is less adherent than NBCA, and so a greater degree of reflux around the microcatheter during injection can be tolerated with less risk of catheter retention. Unlike NBCA, Onyx can be injected slowly, and the injection can be interrupted to perform angiographic runs to view the progress of embolization. Because of these properties, a greater degree of embolization can be achieved from a single vessel with Onyx than with NBCA, necessitating fewer vessel catheterizations to achieve the same degree of embolization, as a rule. Despite these advantages, Onyx has been reported to cause DMSO-related angiotoxicity and pulmonary edema and has the potential to create sparks during surgery if contacted by monopolar, or less frequently bipolar, cautery. Furthermore, Onyx has a propensity to penetrate arterial feeders in a retrograde fashion or venous outflow channels, which if not recognized may result in nontarget embolization causing potentially significant ischemic complications.
Embolization Goals
Preoperative endovascular tumor embolization can be used to decrease overall blood loss; to improve visualization at surgery thus facilitating tumor resection; and/or to selectively occlude deep, inaccessible arterial feeders to the tumor. Transarterial embolization has been the traditional method to achieve these goals. Targeted embolization and occlusion of deep, prominent arterial feeders not accessible until late during the course of surgery is particularly useful for selected hypervascular tumors, where delicate microdissection and selective preservation of the normal, nontumor vasculature are necessitated by the site and local anatomy of the lesion. When multiple arterial feeders exist, transarterial occlusion of some may or may not result in significant overall tumor devascularization if others are left patent; however, if the remaining patent vessels are readily accessible at surgery, there may still be a significant benefit to selective embolization of only the deep feeders.
Even when near-complete or complete angiographic devascularization is achieved after preoperative feeding artery occlusion, surgeons may still note that the tumor bleeds significantly at surgery, reflecting collateralization and/or angiographically occult vascularization after embolization. It has been suggested but not substantiated that intraparenchymal tumor penetration of the embolic agent results in less operative blood loss compared with arterial feeding artery occlusion alone. Furthermore, it has been reported that intraparenchymal tumor penetration with Onyx is difficult to achieve by a transarterial route unless the microcatheter is situated within 2 cm of the tumor. In our experience, intraparenchymal tumor penetration of Onyx is best achieved by direct tumor puncture, which is an option in certain types of tumors ( Box 3 ), but obviously not all tumors can be accessed directly. Another advantage of embolization by direct puncture is that it offers the opportunity to achieve significant tumor devascularization while avoiding the need to catheterize multiple arterial feeders to the lesion, which may be difficult or dangerous to access transarterially.
Juvenile nasal angiofibromas
Carotid body tumors
Glomus vagale tumors
Other head and neck tumors
Tumor embolization procedure details
Anesthesia
We prefer to perform all tumor embolization procedures with the patient fully anesthetized and intubated. This minimizes patient motion and allows for intermittent suspension of the patient’s respirations, which greatly enhances angiographic visualization during embolization. Furthermore, the DMSO in Onyx is angiotoxic and makes injection of this embolic agent quite painful and poorly tolerated in awake patients. For cooperative patients, intravenous sedation and appropriate analgesia without general anesthesia may be considered in selected cases, such as proximal segmental spinal artery occlusions using NBCA.
Angiography
Percutaneous transfemoral artery angiography is performed to delineate the extent of tumor blush, arterial supply, tumor flow dynamics, and venous drainage, and to identify important normal vasculature to be preserved. Using standard endovascular techniques, 5F guide catheters and DMSO-compatible microcatheters are generally used to access the target vessels leading to the tumor. Intravenous heparinization is initiated to achieve and maintain an activated clotting time of 200 to 300 seconds. A microangiogram should always be performed before embolization to ascertain tumor vascularity and identify any dangerous anastomoses to the adjacent normal vasculature.
Embolization
Liquid embolic embolization should be performed as close to the lesion as possible to achieve maximal intratumoral penetration of embolic material. Direct tumor puncture can be performed in selected cases using an 18-gauge spinal needle, with subsequent angiography and embolization carried out through the needle, as detailed previously. We typically use NBCA for distal feeding artery occlusion in cases where Onyx embolization is believed to be either too risky or unnecessary. For example, if the local vascular anatomy is such that deep intratumoral penetration of Onyx poses a high risk of nontarget embolization into important adjacent vessels, or if there is not enough of a safe distance proximally on the target vessel to allow for enough Onyx reflux to form an adequate “plug” (which must occur before the Onyx is able to be “pushed” forward), then we favor NBCA to achieve a focal occlusion of the target vessel. In selected tumors with rapid arteriovenous shunting, in which there is concern that an injected liquid embolic agent may inadvertently flow through the lesion and into the venous side, coils may be deployed first to partially devascularize the tumor, making it safer to then use the desired liquid embolic agent.
In those instances where distal selective catheterization is not possible, we prefer to use PVA particles for preoperative tumor embolization. This requires a slightly larger microcatheter than those used for liquid embolic embolization and also demands a careful review of the local vascular anatomy to identify potentially dangerous collaterals and to choose appropriately sized particles.
Postprocedure Care
After embolization, follow-up angiography demonstrates the extent of tumor devascularization and is also necessary to evaluate patency of the important adjacent normal vasculature. Intravenous steroids are often given to mitigate the expected peritumoral edema that occurs as a consequence of embolization. Routine postangiography care includes groin and distal pulse checks and frequent neurologic examinations to detect any clinical deterioration, which may be secondary to ischemia, hemorrhage, or postembolization tumor swelling.

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