Anterior and Subtemporal Approaches to the Infratemporal Fossa

Published on 13/06/2015 by admin

Filed under Surgery

Last modified 22/04/2025

Print this page

rate 1 star rate 2 star rate 3 star rate 4 star rate 5 star
Your rating: none, Average: 5 (1 votes)

This article have been viewed 3261 times

Chapter 54 Anterior and Subtemporal Approaches to the Infratemporal Fossa

The infratemporal fossa (ITF) is a potential space bounded superiorly by the greater wing of the sphenoid and the temporal bone. Neurovascular foramina, including the carotid canal, jugular foramen, foramen spinosum, foramen ovale, and foramen lacerum, connect the ITF with the middle cranial fossa. Medially, the ITF is contained by the superior constrictor muscle, the pharyngobasilar fascia, and the pterygoid plates. Medially, the ITF communicates with the pterygopalatine fossa via the pterygomaxillary fissure, which is continuous with the inferior orbital fissure and the orbit. Laterally, the ITF is bounded by the zygoma, mandible, parotid gland, and masseter muscle. The pterygoid muscles constitute the anterior boundary; posteriorly, the ITF is confined by the articular tubercle of the temporal bone, glenoid fossa, and styloid process. Using this definition, the ITF contains the parapharyngeal space (i.e., internal carotid artery [ICA], internal jugular vein, CN IV to XI) and the masticator space (i.e., internal maxillary artery, pterygoid venous plexus, and pterygoid muscles).

The presence of neurovascular structures within the ITF (e.g., ICA) or adjacent to it (e.g., CN VII) is the limiting step for designing a surgical approach to the ITF. Surgical approaches often center on the preservation and identification of these neurovascular entities. The first report in the English literature of a surgical approach to the ITF is attributed to Barbosa,1 who in 1961 described his approach for advanced tumors of the maxillary sinus. Transtemporal approaches described by Fisch and preauricular approaches by Schramm and Sekhar are the basis for other modifications.28 Subsequent approaches follow the surgical and anatomic principles shown by these authors.

PREOPERATIVE EVALUATION

Diagnostic and Staging Work-up

Owing to the inaccessibility of the ITF to physical examination, radiographic imaging is a vital component of the evaluation. Computed tomography (CT) and magnetic resonance imaging (MRI) provide valuable information and are obtained using standard skull base protocols. CT is superior to MRI, showing the remodeling or erosion of neurovascular foramina or other bones of the skull base. MRI better delineates the soft tissue planes, the tumor–soft tissue interface, and the presence of tumor along neural and vascular structures (Fig. 54-1). CT and MRI are often complementary.

Another crucial question is the relationship of the tumor to the ICA. Magnetic resonance angiography (MRA) and computerized tomography angiography (CTA) provide a noninvasive assessment of the vasculature of the ITF and brain. If preoperative embolization of the tumor is indicated (e.g., juvenile nasopharyngeal angiofibromas, paragangliomas), angiography is preferred over MRA. Angiography provides important information regarding the vascularity of the tumor, its relationship to the ICA, and the cerebral circulation and its collateral blood supply. Neither angiography nor MRA is adequate, however, to predict reliably the adequacy of the collateral intracranial circulation if sacrifice of the ICA is necessary.

If the risk for injury or sacrifice of the ICA is high, the collateral cerebral blood flow may be evaluated using angiography-balloon occlusion with xenon CT (ABOX-CT). A nondetachable balloon is inserted in the ICA via the femoral artery. The balloon is inflated for 15 minutes while the awake patient is monitored for any neurologic deficit. If the patient does not develop any deficit, the balloon is deflated, and the patient is transferred to a CT suite. A mixture of 32% xenon/68% oxygen is administered via facial mask for 4 minutes. CT shows the distribution of xenon, which reflects the blood flow within the cerebral tissue, providing a quantitative assessment of milliliters of blood flow per minute per 100 g of brain tissue. The process is repeated after reinflation of the arterial balloon. A computer calculates the differential of the xenon diffusion in the brain before and after the balloon inflation, identifying patients at risk for an ischemic stroke secondary to reduced blood flow after occlusion of the ipsilateral ICA (Table 54-1).9

TABLE 54-1 Xenon Computed Tomography

Cerebral Blood Flow (mL/min/100 g Tissue) Risk Implication
>35 Low Carotid may be sacrificed
21-35 Moderate Patient would tolerate occlusion under controlled circumstances; reconstruction is recommended
≤20 High Patient would not tolerate occlusion of internal carotid artery

Despite a negative finding from ABOX-CT testing, patients can sustain ischemic brain injury because of the loss of collateral vessels that are not assessed by balloon occlusion testing (“watershed area”), or because of embolic phenomena. In addition, this test is performed under ideal and controlled circumstances, and does not account for the possibility of episodes of hypoxia, hypotension, or electrolyte and acid-base disturbances that may alter the brain’s hemodynamics. Every effort should be made to preserve or reconstruct the ICA and to diminish the possibility of embolus formation during the surgery. Other techniques that provide information regarding collateral cerebral blood flow include single photon emission CT (SPECT) with balloon occlusion and transcranial Doppler.

Histologic diagnosis should be obtained before the extirpative surgery whenever possible. Tumors amenable to a punch or open biopsy are approached in this manner. Tumors that are in deeper planes may be sampled by fine-needle aspiration biopsy. Rarely, a histologic diagnosis cannot be obtained before the approach because of the intrinsic limitations of fine-needle aspiration biopsy. Under these circumstances, a frozen section analysis, obtained via a skull base approach, may be sufficient to justify the resection of the tumor. Vital neurovascular structures, such as the ICA, the eye, and cranial nerves, should not be sacrificed, however, based on a frozen section analysis.

The extent of the evaluation to rule out regional or distant metastasis or to determine that the ITF tumor is a metastasis is dictated by the histologic type and stage of the tumor. CT scan of the neck is more sensitive than physical examination for the detection of regional lymphadenopathy. Patients presenting with tumors that metastasize hematogenously (sarcoma, melanoma) should undergo CT scan of the chest and abdomen and a bone scan. Cerebrospinal fluid (CSF) cytology is advised for patients with tumors that have invaded the dura. These patients are also at risk for “drop metastasis,” which should be ruled out by spinal MRI.

Rehabilitation Considerations

Functional or neurologic deficits that are identified preoperatively should be taken into consideration during the surgical planning and during postoperative care. These deficits often have a significant impact on the recovery and functional rehabilitation of the patient.

Dysfunction of the trigeminal nerve or the masticator muscles or both is commonly underdiagnosed. Cutaneous and corneal sensation should be assessed preoperatively. Corneal anesthesia associated with concomitant facial nerve palsy requires aggressive measures to prevent corneal injury.

Lateral deviation of the jaw on opening may reflect weakness or paralysis of the ipsilateral pterygoid muscles, invasion of the muscles, or dysfunction of the temporomandibular joint (TMJ). Likewise, trismus may be due to mechanical restriction caused by the bulk of the tumor, ankylosis of the TMJ, scarring, tumor tethering, or pain. The nature of the trismus is an important consideration in the perioperative management of the airway. Trismus secondary to pain resolves with the induction of general anesthesia, allowing safe oral endotracheal intubation. In patients with mechanical trismus, an awake nasotracheal intubation may be performed if it is anticipated that surgery would correct the trismus. Otherwise, a tracheostomy, performed under local anesthesia, is the safest perioperative airway.

Neoplastic invasion of the facial nerve may manifest with facial weakness or paralysis, facial spasms, epiphora, facial spasms, and dysgeusia. Significant destruction of the facial nerve by tumor may occur before the patient develops these clinical signs. A gold weight, implanted in the upper eyelid, or surgical tightening of the lower lid may be necessary to protect the cornea.

Hearing loss caused by a tumor of the ITF may be either conductive, resulting from eustachian tube dysfunction, or sensorineural, resulting from tumor involvement of the temporal bone or posterior cranial fossa. A myringotomy or amplification or both facilitate communication with the patient.

Deficits of the lower cranial nerves (CN IX, X, XI, and XII) are associated with tumors that originate in the parapharyngeal space or tumors that extend to the jugular foramen, or both. Patients with deficits of CN IX, X, and XII present with varying degrees of swallowing or speech problems, such as hypernasal or slurred speech, nasal regurgitation, dysphagia, aspiration, and dysphonia. Findings on physical examination reflect the involvement of specific cranial nerves, and include decreased elevation of the palate, decreased mobility and strength of the tongue with deviation to the involved side on protrusion, decreased supraglottic sensation, pooling of secretions in the hypopharynx, ipsilateral vocal cord paralysis, and decreased bulk and strength of the sternocleidomastoid and trapezius muscles. Patients with partial deficits of the lower cranial nerves (paresis) often experience a complete deficit (paralysis) after surgery, resulting in increased dysphagia and aspiration. Consequently, a tracheostomy for tracheal toilet and a gastrostomy tube for nutrition and hydration are often necessary during the perioperative period.

Laryngeal framework surgery (thyroplasty) performed during the extirpative surgery or the early postoperative period improves the glottic closure and decreases the risk for aspiration, often obviating the need for a tracheotomy for the sole purpose of tracheopulmonary toilet.1012 Laryngeal framework surgery allows the patient to compensate for the deficits using the remaining function (contralateral side) more effectively. Laryngeal framework surgery does not restore the motor or the sensory function. These patients remain at a higher risk for aspiration and nutritional deficiencies. Collaboration with an experienced speech-language pathologist, who can assist with the monitoring of the patient and the diet modifications and provide intensive swallowing therapy, is crucial to prevent the pulmonary and nutritional complications of aspiration. In patients with severe deficits or in patients with cognitive problems, strong consideration should also be given to placement of a gastrostomy tube to facilitate postoperative feeding and decrease the risk of prandial aspiration.

Velopharyngeal insufficiency may be ameliorated by a palatal lift prosthesis that pushes the soft palate against the posterior pharyngeal wall. Alternatively, a pharyngeal flap or a palatopexy may be performed in patients who do not tolerate the prosthesis.

Reconstructive Considerations

Most commonly, a temporalis muscle transposition flap is adequate to separate the cranial cavity from the upper aerodigestive tract and obliterate the dead space. Microvascular free flaps, such as rectus abdominis flap (for soft tissue defects), latissimus dorsi flap (for myocutaneous or massive defects), and iliac composite flap (for defects requiring bone reconstruction), are indicated when the temporalis muscle or its blood supply is sacrificed as part of the oncologic resection, when the patient requires a complex resection involving composite tissue flaps with skin or bone or both, or when the extirpative surgery leads to a massive soft tissue defect and dead space. These needs are usually anticipated during the surgical planning, and the patient and consultants (e.g., the microvascular surgeon) are informed accordingly.

Ideally, functional and cosmetic deficits created by the tumor or the surgery should be addressed in a single stage, concomitant with the oncologic resection. When a temporary facial palsy is anticipated, corneal protection using lubricants or a temporary lateral tarsorrhaphy or both is usually adequate. Grafting of the facial nerve involves a longer recovery period, however. Insertion of a gold weight implant into the upper eyelid is advisable. When an immediate reconstruction of the facial nerve is impossible, static fascial slings or muscle transpositions are indicated. Lower cranial nerve deficits may be ameliorated by laryngeal framework surgery, tracheotomy, or laryngotracheal separation, as previously discussed.

Other Perioperative Considerations

Preoperatively, the patient’s blood is typed and crossmatched for 2 to 6 U of packed red blood cells, according to the extent and nature of the tumor and surgery. Autologous blood banking is used when feasible, although it is frequently impractical. A Cell Saver autologous transfusion device may be used during the resection of benign vascular tumors.

Perioperative antibiotic prophylaxis with a wide spectrum against the flora of the skin and upper aerodigestive tract and that exhibits good penetration of the blood-brain barrier is administered before the surgery and is continued for 48 hours after the surgery. The use of a broad-spectrum cephalosporin with good CSF penetration (e.g., ceftriaxone) seems to be as effective as multiple antibiotic regimens.

Somatosensory evoked potential monitoring using the median nerve is indicated whenever surgical manipulation of the ICA is anticipated. Lower cranial nerve monitoring is not routinely employed. It may be useful for the identification and preservation of nerve function when the tumor is in close proximity to these nerves. Conversely, facial nerve monitoring is routinely used for transparotid or transtemporal approaches. Monitoring electrodes and lines for vascular access should be secured with sutures, staples, or adhesive dressings.

The choice of anesthetic agent is influenced by the extent of intracranial dissection, potential for brain injury, systemic hemodynamics, the need for monitoring of cortical and brainstem functions (e.g., brainstem-evoked response, somatosensory evoked potentials, electroencephalography), and the need for cranial nerve monitoring (CN VII, and X to XII). All these factors should be thoroughly discussed with the anesthesiologist.

When changes of head position during surgery are anticipated, the endotracheal tube should be secured with a circumdental or circum-mandibular wire ligature (No. 26 stainless steel wire). The operating table is positioned perpendicular to the anesthesia staff, and if intradural dissection is anticipated, a spinal drain is inserted and secured with sutures and adhesive dressing (e.g., Tegaderm, Op-Site). Other measures to diminish the intracranial pressure, such as hyperventilation, osmotic diuresis, and corticosteroids, are used as needed throughout the surgery.

A nasogastric tube and Foley catheter are passed and secured after adequate placement is corroborated. Antiembolic sequential compression stockings are recommended to prevent deep venous thrombosis.

SURGICAL APPROACHES

The head of the patient is positioned on a horseshoe headrest or, if necessary for intracranial neurovascular or neurosurgical work, on a three-pin head fixation system. When the horseshoe headrest is used, it is important to use additional “egg-crate” foam padding because the scalp may develop a decubitus ulcer during prolonged surgery. If the ICA is at risk, the head should be positioned in slight extension to provide access to the neck for proximal control of the ICA. Tarsorrhaphy sutures are placed for protection of the eyes. The scalp is shaved following the planned incision line (e.g., bicoronal), and the incision line is infiltrated with a solution of lidocaine and epinephrine (1:100,000 to 1:400,000).

Preauricular (Subtemporal) Approach

The preauricular approach is suited for tumors that originate in the ITF and intracranial tumors that originate at the anterior aspect of the temporal bone, or greater wing of the sphenoid bone, and that extend into the ITF.5,13,14 It may also be combined with other approaches, such as a subfrontal approach to expose massive tumors that extend to the anterior and middle skull base. The preauricular approach does not provide an adequate exposure for the resection of tumors that invade the tympanic bone, however, and does not provide control of the intratemporal facial nerve or jugular bulb.

An incision, following a hemicoronal or bicoronal line, is carried through the subcutaneous tissue, galea, and pericranium (Fig. 54-2). Over the temporal area, the incision extends down to the deep layer of the temporal fascia. The anterior branches of the superficial temporal artery are preserved, ensuring adequate blood supply to the scalp flap. Ipsilateral to the tumor, the incision is extended following into the preauricular crease down to the level of the tragus. When proximal control of the ICA is warranted, the incision is extended into the neck using a lazy S pattern, or, alternatively, a separate cervical incision is performed. The scalp is dissected following a subpericranial plane, separating the attachments of the pericranium to the deep layer of the temporal fascia. The scalp flap is elevated from the deep temporal fascia using a broad periosteal elevator.

Above the zygoma, the deep temporal fascia splits into superficial and deep layers, which attach to the lateral and medial surfaces of the zygomatic arch. To continue the surgical exposure, the superficial layer of the deep temporal fascia is incised following an imaginary line that joins the superior orbital rim to the zygomatic root. The dissection continues deep to this plane, elevating the superficial layer of the deep temporal fascia off the zygomatic arch (see Fig. 54-2). Fascia and periosteum are reflected anteriorly with the scalp flap. This maneuver protects the frontal branches of the facial nerve that are just lateral to the superficial layer of the deep temporal fascia. Elevation of the periosteum from the lateral surface of the zygomatic arch and malar eminence completes exposure of the orbitozygomatic complex. The periorbita is elevated from the lateral orbit using a Penfield No. 1 dissector, exposing the roof and lateral wall of the orbit down to the inferior orbital fissure.

The fascial attachments of the temporalis and masseter muscles to the zygomatic arch are transected using electrocautery. The attachments of the temporalis muscle to the cranium are transected with the electrocautery, and the muscle is elevated off the temporal fossa. If the temporalis muscle is to be returned to its original position at the completion of the surgery, a curved titanium plate (1.5 to 1.7 mm) is screwed at the temporal line, leaving some screw holes empty to facilitate suturing from the plate to the muscle (Fig. 54-3). Then the masseteric fascia is dissected from the masseter muscle, elevating the overlying parotid gland with a broad periosteal elevator (see Fig. 54-2). To increase the arc of rotation of the scalp flap, any soft tissue anterior to the tympanic bone can be transected from superior to inferior, down to the level of the facial nerve. The facial nerve is identified and preserved using a standard technique. It is helpful to preserve a cuff of soft tissue around the main trunk of the facial nerve to prevent a traction injury to the main trunk of the facial nerve.

Using the caudal limb of the incision, the sternocleidomastoid muscle is dissected laterally, and the carotid sheath is exposed. When necessary, the contents of the carotid sheath, including the ICA and common and external carotid arteries, and the internal jugular vein are exposed, dissected, and controlled. CN X to XII are also identified and preserved. Vessel loops are placed around these structures and secured with hemoclips rather than hemostats to avoid inadvertent traction.

Orbitozygomatic osteotomies are performed at the zygomatic root posteriorly, the zygomaticofrontal suture superiorly, and the zygomaticomaxillary buttress at the level of the zygomaticofacial nerve medially (see Fig. 54-3). Prior periorbital elevation off the lateral and inferior walls is necessary to identify the inferior orbital fissure and to complete the osteotomies of the orbitozygomatic complex. The tip of the reciprocating saw is placed in the most lateral aspect of the inferior orbital fissure; an osteotomy is performed through the malar eminence following a vertical imaginary line medial to the zygomaticofacial foramen. This osteotomy separates the zygoma from the maxilla. Accidental entry into the maxillary sinus may occur, requiring closure of the defect using fascia or pericranium free grafting or both. These free tissue grafts are held in place by compression against the opening when orbitozygomatic bone graft is replaced and plated at the completion of the surgery. All osteotomies are completed with a reciprocating saw transecting the bone in beveled or V-shaped manner in such a way that maximizes the exposure and facilitates replacement of the bone graft at the completion of the surgery. If tumor involvement of the orbit is present, the osteotomies are modified to secure a complete resection.

In cases requiring intracranial and extracranial exposure, the superior and lateral osteotomies are made through the superior and lateral orbital walls after the craniotomy is completed, and the brain is separated from the skull base. This way, the orbital walls can be incorporated in the orbitozygomatic graft. Using intracranial and extracranial exposures, osteotomies are made through the superior and lateral orbital walls to remove the orbitozygomatic bone segment. This approach provides excellent access to the infratemporal skull base, orbital apex, and lateral maxilla.

The temporalis muscle is reflected inferiorly until the infratemporal crest is fully visualized. A subperiosteal plane is followed to dissect the soft tissues from the infratemporal cranium. Bleeding from the underlying bone is controlled by the application of bone wax.

Fracturing or removal of the coronoid process increases the arc of rotation of the temporalis muscle. Care should be exercised when dissecting the medial aspect of the temporalis muscle, especially near its insertion (coronoid process) because the blood supply to the muscle (deep temporal artery from the internal maxillary artery) penetrates the muscle at this area. Likewise, the soft tissue at the sigmoid notch should be dissected carefully to prevent accidental injury to the internal maxillary artery that travels adjacent to the medial surface of the mandibular ramus.

Dissection of the soft tissues from the infratemporal skull base is usually associated with troublesome bleeding arising from the pterygoid plexus. Bleeding is controlled with the use of bipolar cautery or Cottonoids moistened in oxymetazoline 0.05%, or both. Unipolar cautery is seldom used because it stimulates V3, causing contraction of the mastication muscles and occasional cardiac arrhythmias.

A subtemporal craniectomy may aid in the identification of neurovascular structures piercing the infratemporal skull base and to augment the exposure. The lateralmost bone is removed using rongeurs. The origin of the lateral pterygoid plate at the skull base is identified anteriorly. Anatomic relationships that are useful for the identification of infratemporal skull base structures are shown in Figure 54-4, including the posterior curve of the attachment of the lateral pterygoid plate that is in alignment with the foramen ovale, foramen spinosum, and the spine of the sphenoid bone. These structures lie in a straight “line of sight” that is lateral to the canal of the ICA. The inferolateral aspect of the sphenoid sinus may be accessed by removing the bone (i.e., pterygoid plates) between the second and third divisions of the trigeminal nerve. The extirpation of the tumor can now proceed, including the involved soft tissue and bone. To continue the subtemporal exposure, the middle meningeal artery is clipped or cauterized using bipolar electrocautery and transected. Bleeding from the venous plexus that accompanies V3 through the foramen ovale may be controlled with absorbable knitted fabric (Surgicel) packing.

Lesions that do not involve the temporal bone or petrous portion of the ICA are adequately exposed with this stepwise approach. Dissection of the petrous ICA is necessary, however; the glenoid fossa is removed as part of the orbitozygomatic bone graft. It is first necessary to perform a temporal craniotomy for exposure of the superior aspect of the glenoid fossa (Fig. 54-5). The capsule of the TMJ is dissected free from the fossa and displaced inferiorly. If possible, the capsule and meniscus are preserved. With use of a reciprocating saw, osteotomies are made through the glenoid fossa, incorporating the lateral two thirds of the fossa (see Fig. 54-5). This maneuver avoids potential injury to the ICA that is located medial to the fossa. In addition, this modification provides stability for the mandibular condyle after reconstruction, although it can be prone to anterior dislocation. Injury to the cochlea is possible if the osteotomies are made too posteriorly. If additional exposure is necessary (i.e., carotid canal and extratemporal ICA), the condylar neck and contents of the condylar fossa can be transected at the level of the sigmoid notch and removed (Fig. 54-6).

To dissect the petrous segment of the ICA, it is necessary to transect the mandibular division of the trigeminal nerve at the foramen ovale (see Fig. 54-6). When the ICA is mobilized from its horizontal canal, it can be transposed or retracted to facilitate the resection of tumor, or to gain access to the petrous apex.

Approaches to the ITF are modified according to the extent of the tumor and other clinical circumstances. Tumors that invade the mandible mandate a partial mandibulectomy to obtain negative margins. In a pediatric patient, the distance from the body of the mandible to the infratemporal skull base is greatly foreshortened. Adequate exposure of the infratemporal skull base can often be achieved using a transcervical approach with superior transposition of the facial nerve.

After extirpation of the tumor, it is necessary to close any communication with the upper aerodigestive tract. If viable, a temporalis muscle flap is used to obliterate the dead space and protect the ICA (Fig. 54-7). Because of the branching pattern of the blood supply to the temporalis muscle, the muscle can be divided vertically, and the anterior half of the muscle may be transposed with an intact blood supply. The remaining posterior half of the muscle is transposed anteriorly to fill the temporal fossa defect.

Defects of the orbital floor may be reconstructed with titanium mesh, which is then covered with a temporalis muscle transposition flap or temporoparietal fascia flap. Likewise, defects of the lateral orbital wall can be reconstructed with titanium mesh. In selected patients, anteriorly or posteriorly based pericranial scalp flaps may be elevated to provide protection of the infratemporal skull base. When the temporalis muscle is unavailable, massive soft tissue defects are best reconstructed with microvascular free tissue flaps.

The orbitozygomatic bone graft is replaced and fixated in its original position with titanium alloy adaptation plates, wire, or braided nylon sutures. Plating of the bone grafts is preferred because it provides greater stability. To avoid compression of reconstructive flaps, it is sometimes necessary to remove a portion of the zygomatic arch.

If resection of the mandibular condyle was necessary to expose the petrous ICA, reconstruction of the TMJ is not attempted. Reconstruction of the TMJ after oncologic exenteration of the ITF does not improve the postoperative function significantly, and may lead to scarring, ankylosis, and trismus.

Periosteal and muscular attachments to the craniofacial skeleton must be repaired to prevent retraction or sagging, or both, of the muscles and other soft tissues. The skin and mucosal incisions are closed using a multilayered technique

Postauricular (Transtemporal) Approach

The postauricular approach is designed to expose and resect lesions involving the temporal bone and extending into the ITF.3,14 A question mark–shaped or C-shaped incision is started in the temporal area and extended, postauricularly, into the mastoid region, curving down to follow one of the midneck horizontal skin creases (Fig. 54-8).

If the middle ear is to be sacrificed as part of the approach or the tumor resection, and there is a risk of a postoperative CSF leak (intradural work), the external auditory canal (EAC) is closed permanently to prevent CSF otorrhea. The EAC is divided at the bony-cartilaginous junction and then closed using everting stitches. This closure is reinforced with a myoperiosteal U-shaped flap based on the posterior margin of the EAC. Alternatively, if the middle ear is to be spared, the canal may be preserved by placing the incisions in the conchal area (Fig. 54-8B). The incision follows the margin of the conchal bowl and tragus so that the scar would be hidden.

In the conchal area, the skin, cartilage, and perichondrium are incised to communicate with the retroauricular plane of dissection. These incisions, placed laterally, facilitate the anastomosis of the EAC to the pinna at the end of the extirpative procedure. An incision inside the EAC is not recommended because it is difficult to suture in a watertight manner, and tends to stenose. A Penrose drain can be inserted through the conchal defect in the skin-auricle flap to facilitate its retraction. Elevation of the cervicofacial flap is carried in a subplatysmal plane in the cervical area, suprasuperficial musculoaponeurotic system plane over the parotid area, and following the deep layer of the deep temporal fascia over the cranium.

The main trunk of the facial nerve is identified anterior to the EAC just distal to the stylomastoid foramen, as is described for a parotidectomy. If circumferential mobilization of the main trunk is unnecessary, a cuff of soft tissue is preserved around its main trunk to minimize the possibility of a traction injury when the facial flap is retracted anteriorly. In selected cases, a “tail” parotidectomy may enhance the access to the retromandibular area. A total parotidectomy is indicated when facing an epithelial malignancy of the parotid gland. Skeletonization of the main trunk of the facial nerve and its branches facilitates their retraction and the access to the ITF. Resection of the main trunk of the facial nerve and its branches (radical parotidectomy) is indicated when the nerve is invaded by the tumor.

Attention is then directed to the cervical exposure to obtain proximal control of the common, internal, and external carotid arteries, and the internal jugular vein. CN X to XII are identified and preserved. The sternocleidomastoid and digastric muscles are transected at their insertion to the mastoid bone. The stylohyoid and stylopharyngeus muscles are transected, and the styloid process is removed. CN IX usually can be identified at this time, as it crosses lateral to the ICA.

A mastoidectomy and dissection of the vertical portion of the facial nerve allows the transposition of the facial nerve, providing a wider access to the infratemporal fossa (see Fig. 54-9). In patients who require a radical parotidectomy, a mastoidectomy provides the means to obtain proximal control of the neural margins and to graft the nerve. It also provides access to the jugular bulb and adjacent lower cranial nerves.

Orbitozygomatic osteotomies may be performed as previously described (preauricular approach). After the orbitozygomatic complex is removed, the anterior, superior, medial, and posterior boundaries of the infratemporal fossa are well exposed, and all major vessels are “controlled.” Completion of the infratemporal skull base approach, including a temporal craniotomy, is performed as described in the previous section. The extirpation of the tumor can now proceed, including the involved soft tissue and bone. Reconstruction of the defect follows the principles outlined in previous sections.

Lateral Fisch Infratemporal Fossa Approaches

Fisch has described an array of lateral infratemporal fossa approaches that are the prototypic otologic approaches to the ITF (Fig. 54-8,9,10)3. The hallmark of these approaches is temporal bone management emphasizing facial nerve rerouting and subtemporal dural exposure for wide access to the lateral skull base. Figure 54-10 illustrates the anatomic regions appropriate for the Fisch type A, B, and C approaches. The Fisch type A approach has been described in detail in Chapter 46 regarding its application in glomus jugulare surgery. The Fisch type B and C approaches are designed to approach more anterior pathology involving the petrous apex and clivus. The type C approach is an extension of the type B approach, and is used for lesions of the anterior ITF, sella, and nasopharynx. The Fisch type D is a preauricular ITF approach using an orbitozygotomy and resection of the floor of the middle fossa for medial dural exposure without a lateral temporal craniotomy.

Fisch Type B

The principal exposure maneuver in the Fisch type B ITF approach is reflection of the zygomatic arch and temporalis muscle inferiorly and removal of the bone of the skull base floor to provide access to the ITF. The incision is wide and C-shaped beginning at the angle of the mandible and extending retroauricularly and anterior laterally to the eyebrow. The ear canal is transected and closed in the same manner as described in Chapter 47 in a two-layer technique.

The main trunk of the facial nerve is identified using standard landmarks at the stylomastoid foramen. The superior division is followed to the level of the frontalis branch. With this direct visualization, the periosteum attached to the zygomatic arch is reflected down to protect the frontalis branch of the facial nerve. At this point, the osteotomies of the zygomatic arch can be completed anteriorly as close as possible to the orbital rim and posteriorly at the root of the zygoma. The masseter muscle is left attached at the zygomatic arch to be reflected inferiorly. The temporalis muscle is completely reflected inferiorly, carefully protecting its blood supply.

A key to this extradural exposure is the subtotal “petrosectomy.” This step includes a canal wall down mastoidectomy including complete skeletonization of the labyrinth, facial nerve, sigmoid sinus, middle fossa, and posterior fossa dura and the jugular bulb, and exenteration of all hypotympanic air cells and skeletonization of the ICA. The unique aspect is that by removing the ossicular chain and middle ear structures, the carotid artery can be skeletonized completely beyond the genu to the foramen lacerum.

The TMJ is disarticulated by incising the capsule and removing the articular disc. At this point, the bone of the glenoid fossa and the root of the zygoma are completely removed with cutting and diamond burrs. Middle fossa dura in the subtemporal region is completely skeletonized. By placing the infratemporal fossa retractor over the mandibular condyle, additional skeletonization of the middle fossa dura can be accomplished medially until reaching the middle meningeal artery and V3 at the foramen ovale. Cauterization of the middle meningeal artery and transection of the mandibular nerve permit greater exposure. At this point, further skeletonization of the carotid artery is possible along the lateral and anterior wall of the ICA. Complete exposure of the carotid artery permits its mobilization out of the carotid canal, providing free access to the petrous apex and clivus. The eustachian tube must be sutured closed to prevent infection of the nasal cavity. Although the bone defect is filled with abdominal fat, temporalis muscle is used to cover the fat and is placed inferior to the skeletonized middle fossa dura and mandibular condyle. The zygomatic arch can be secured with microplates, and the skin can be closed in a standard fashion.

Anterior Transfacial Approach (Facial Translocation)

The anterior transfacial technique is best used to approach sinonasal tumors invading the ITF, the masticator space, or the pterygomaxillary fossa, and for tumors of the nasopharynx extending into the ITF (Fig. 54-11).7,13,14 A bicoronal incision with an ipsilateral preauricular extension is performed and extended through the subcutaneous tissue (see the section on preauricular approach). A Weber-Fergusson incision is completed and extended down to the periosteum of the maxilla, nasal bones, and orbital rim. During a “traditional” translocation approach, a horizontal incision is carried over the superior edge of the zygomatic bone, extending into the lateral canthus, to meet the Weber-Fergusson incision (see Fig. 54-11). The frontal branches of the facial nerve are identified and dissected as they cross over the zygomatic arch. They are then entubulated with silicone tubing and transected. These nerve branches are reanastomosed at the end of the case, using an entubulation technique.

Subperiosteal dissection of the anterior maxilla exposes the infraorbital nerve, which is then transected and tagged to facilitate its identification and reanastomosis at the end of the case. Then, an inferiorly based flap including the upper third of the upper lip, entire cheek, lower eyelid, parotid gland, and facial nerve is reflected inferiorly. The frontotemporal scalp flap is elevated in a subpericranial plane. This flap is reflected anteriorly, exposing the superior orbital rims (see Fig. 54-11). Alternatively, the exposure can be achieved without the temporal incision by combining the preauricular approach with the anterior exposure provided by the Weber-Fergusson incision.

Orbitozygomatic osteotomies are performed and joined with the maxillary osteotomies to free the anterior face of the ipsilateral maxilla en bloc with the orbitozygomatic complex. Alternatively, the maxillary bone graft can be elevated as a vascularized graft attached to the cheek flap, as described by Catalano and Biller.8 The temporalis and masseter muscles are dissected from the zygomatic bone with electrocautery. Osteotomies are completed, and the bone graft is removed. The temporalis muscle is reflected inferiorly. Removal of the coronoid process increases the caudal arc of rotation of the temporalis muscle. After completion of these steps, the anterior, medial, and lateral boundaries of the ITF are well exposed.

In selected cases, the pterygoid plates can be excised to provide further access to the medial ITF or nasopharynx. A temporosubtemporal craniotomy provides additional exposure superiorly and allows dissection of intracranial structures (Fig. 54-12). After the tumor resection, the temporalis muscle may be used to obliterate the surgical defect and provide separation of the cranial cavity from the upper aerodigestive tract, as previously described.

Periosteal and muscular attachments are repaired, and the incisions are closed using a multilayer technique. The conjunctiva is repaired with running 6-0 fast-absorbing suture. The lacrimal canaliculi are stented with Crawford silicone tubing that is tied to itself in the nasal cavity. The eye is closed with a temporary tarsorrhaphy for 10 to 14 days to prevent a lower lid ectropion.

Transorbital Approach

In selected cases, a transorbital approach may be used to complement the exposures obtained with one of the previous approaches enhancing the exposure of the orbital apex and cavernous sinus. This approach consists of transection of the orbital tissues posterior to the globe with preservation of the attachments of the orbital soft tissues, including the globe, to the scalp flap. The orbital apex is removed to provide direct anterior access to the cavernous sinus and cavernous ICA. This approach is reserved for patients with benign tumors of the orbita apex and cavernous sinus who have lost vision as a result of tumor growth. It may also be employed for low-grade malignant neoplasms with minimal involvement of the orbital soft apex or optic nerve to obtain complete tumor removal. Extensive involvement of the orbital soft tissues requires an orbital exenteration. The advantages of this approach include improved cosmesis, a result of the preservation of the globe, and excellent anterior and lateral exposure of the cavernous sinus and its associated structures.

A preauricular infratemporal skull base approach is performed, as previously described. The periorbita is elevated from the superior, lateral, and inferior walls of the orbit. The periorbita is then incised, and the orbital tissues are transected posterior to the globe using bipolar electrocautery and sharp dissection. A cuff of tissue remains at the orbital apex to provide an adequate tumor margin. The remaining periorbital attachments are elevated medially to allow complete displacement of the globe from the orbital cavity. Over the medial wall, the neurovascular bundles are clipped or cauterized and transected. The lacrimal duct is transected, and the sac is marsupialized. Using rongeurs, bone is removed from the lateral wall of the orbit to the superior orbital fissure. The contents of the superior orbital fissure and optic canal are transected to provide additional exposure of the orbital apex.

Because of the loss of orbital bone, enophthalmos results unless the orbital defect is reconstructed with bone grafts or titanium mesh. A temporalis transposition or free tissue transfer provides soft tissue augmentation and protection of the carotid artery.

POSTOPERATIVE CARE

After surgery, the patient is transferred to the intensive care unit for continuous cardiovascular and neurologic monitoring. Laboratory tests to rule out postoperative anemia and electrolyte imbalance are performed. Patients who required multiple blood transfusions should be screened for transfusion-induced coagulation disorders. Mild narcotic analgesia is provided, avoiding sedation that could interfere with a detailed neurologic evaluation.

If the ICA is dissected, ligated, or grafted, close monitoring of the patient’s hemodynamic status and fluid balance is essential. When grafting of the ICA is performed, an angiogram is obtained in the early postoperative period to assess the patency of the graft and detect pseudoaneurysm formation. A CT scan of the brain without contrast medium is performed on the 1st or 2nd postoperative day to screen for intracranial complications, such as cerebral contusion, edema or hemorrhage, fluid collections, or pneumocephalus.

A compressive dressing is maintained for 24 to 72 hours. When the dressing is removed, the wound is cleaned with normal saline solution and covered with antibiotic ointment three to four times a day. The scalp and other wound drains are kept to bulb suction until the drainage is less than 30 mL/day. The drain is then removed, and the wound is closed using an encircling stitch placed at the time of surgery. If the cranial cavity is entered, wall suction is never used because of the risk of direct negative pressure on the central nervous system.

In most cases, the spinal drain is needed only during the surgery and is removed when the procedure is completed. If there is a significant risk of postoperative CSF leak, the spinal drain is kept at the level of the patient’s shoulder, and 50 mL is removed every 8 to 12 hours. The lumbar drain is removed 3 to 5 days after surgery, and the lumbar puncture site is closed with an encircling stitch (e.g., 2-0 nylon), placed at the time of surgery.

Lagophthalmos from weakness or paralysis of the facial nerve may lead to exposure keratoconjunctivitis. Initially, an exposed eye can be protected using artificial tears every 1 to 2 hours, lubrication ointment at bedtime, eye patching, or a moisture chamber. Taping of the eyelids or a temporary tarsorrhaphy is advised if rapid recovery is anticipated. If prolonged paralysis is expected, we prefer a gold weight implant. This procedure can be performed at the time of the original surgery, using a 0.1 to 0.12 g weight (No. 10 or 12), or it may be performed during the early postoperative period. Except in selected cases, we favor the latter because it provides the advantage of being able to establish the exact weight that is needed by the patient.

In most cases, the airway can be secured for the short-term using an endotracheal tube (high-volume/low-pressure cuff). Nevertheless, a tracheotomy is indicated for patients in whom significant edema of the upper aerodigestive tract is anticipated, or if a prolonged mechanical ventilation is anticipated. A tracheotomy also provides better access to the airway for pulmonary toilet for patients with an ineffective cough or severe aspiration.

Patients with high vagal lesions or any combination of deficits of CN IX, X, or XII experience severe swallowing difficulty and aspiration. These patients can be assisted with a medialization laryngoplasty, an arytenoid adduction procedure, or an arytenoidpexy with or without a cricopharyngeal myotomy. Patients who continue to aspirate despite all these measures and who develop repeated aspiration pneumonias are managed by a laryngotracheal separation procedure.

PITFALLS AND COMPLICATIONS

The most common morbidity associated with surgery of the infratemporal fossa is related to deficits of the trigeminal nerve. Sacrifice of the third, sometimes the second, and rarely the first divisions of the trigeminal nerve may be necessary for surgical exposure or to obtain adequate clear margins of resection. Facial anesthesia may predispose the patient to self-inflicted injuries, including neurotrophic ulcers.

The loss of corneal sensation, especially in a patient with paresis of the facial nerve, greatly increases the risk of a corneal abrasion or exposure keratitis. The loss of motor function of the mandibular nerve causes asymmetry of jaw opening and decreased force of mastication on the operated side. Mastication may be impaired further by resection of the TMJ or mandibular ramus. Whenever feasible, sensory and motor divisions of the trigeminal nerve are repaired or grafted after transection for surgical exposure.

Permanent deficits (accidental) of the facial nerve or its branches are uncommon. The frontal branches of the facial nerve are at risk of injury during elevation of the temporal scalp flap. Injury is usually the result either of a dissection in a plane that is superficial to the superficial layer of the deep temporal fascia or of compression during the retraction of the flap. To avoid a traction injury, a cuff of soft tissue is preserved around the main trunk of the facial nerve when a preauricular approach is employed. The facial nerve can also sustain an ischemic injury that occurs as a result of devascularization on mobilization of its infratemporal segments or skeletonization of its extratemporal segments. A temporary paresis of the facial nerve is to be expected with mobilization of the mastoid segment of the facial nerve. Close attention to postoperative eye care is necessary in patients with combined deficits of the trigeminal and facial nerves.

In most patients, surgical resection of the TMJ is not a major factor in the development of postoperative trismus or difficulties with mastication. Rather, mastication seems to be most affected by loss of function of the mandibular division of the trigeminal nerve. Nevertheless, every effort is made to preserve the TMJ. If resection of the glenoid fossa is necessary, the capsule of the TMJ is displaced inferiorly. If resection of the TMJ is necessary, no attempt is made to reconstruct the joint. These patients experience deviation of the jaw to the unaffected side. This is usually of no major consequence, but some patients may need an occlusal guide to help them when chewing.

Postoperative trismus is also a common occurrence because of postoperative pain and scarring of the pterygoid musculature and TMJ. Trismus improves dramatically if patients regularly perform stretching exercises for the jaw. Devices such as the TheraBite appliance are helpful in stretching the scar tissue and forcefully opening the mouth. In severe cases, a dental appliance may be fabricated that is gradually opened by a screw.

Infectious complications are rare. Predisposing factors include communication with the nasopharynx, seroma or hematoma, and a CSF leak. Generally, the dead space should be obliterated to prevent fluid collection that subsequently can be infected, and the cranial cavity should be separated from the sinonasal tract. The use of vascularized tissue flaps is preferred, especially when there has been dissection of the ICA or resection of dura.

Necrosis of the scalp flap is uncommon because of its excellent blood supply. Poorly designed incisions may result, however, in areas of ischemia, particularly around the auricle, which can make the tissue susceptible to secondary infection. Prolonged use of hemostatic clamps can also lead to necrosis of the wound edges.

Neurovascular complications are of the greatest concern. Postoperative cerebral ischemia may result from surgical occlusion of the ICA, temporary vasospasm, and thromboembolic phenomena. Surgical dissection of the ICA can injure the vessel walls, resulting in immediate or delayed rupture and hemorrhage. The ICA is particularly vulnerable to injury where it enters the cranial base. Injuries to the ICA should be repaired primarily (or using a vein graft). An angiogram is obtained in the early postoperative period to assess the adequacy of the repair. If a repair of the ICA is impossible, it should be permanently occluded by ligation or by the placement of a detachable balloon or vascular coil. When the artery is to be permanently occluded, the occlusion is performed as distal as possible (near the origin of the ophthalmic artery). The potential for thrombus formation is less with a short column of stagnant blood above the level of occlusion. After occlusion of the ICA, there is a significant risk of immediate and delayed stroke in patients who do not have more than 35 to 40 mL of blood flow per 100 g of brain tissue per minute by ABOX-CT testing.

After reconstruction of the ICA with a vein graft, there is a risk of postoperative occlusion because of thrombus formation at the suture line, and torsion or kinking of the graft. Pseudoaneurysm formation and delayed blowout of the graft are also risks, especially in the presence of infection. For this reason, reconstruction of the ICA is usually not indicated in a contaminated field with communication to the upper aerodigestive tract. In such cases, permanent occlusion of the ICA or rerouting of a vein graft posterior to the surgical field is performed. An extracranial-intracranial bypass graft to the middle cerebral artery may be performed before tumor resection when sacrifice of the ICA is anticipated. Patients who undergo surgical manipulation of the ICA may also develop cerebral ischemia at the margins of the vascular territories of the cerebral vessels (watershed areas). This ischemia is of particular concern when there is sacrifice of extracranial-intracranial collateral blood vessels, which are not routinely assessed by ABOX-CT as part of the surgical approach. Decreased oxygen delivery because of hypoxic postoperative anemia or hypotension can result in a cerebral infarct in these watershed areas.

A watertight dural closure may be difficult to achieve with large infratemporal skull base defects, particularly around nerves and vessels. An epidural fluid collection may result. In most cases, this fluid collection is contained by the soft tissues and slowly resolves without further intervention. Occasionally, the CSF collection may communicate with the exterior through the EAC, the scalp incision line, or along the eustachian tube to the nasopharynx. Most CSF leaks can be managed nonsurgically by placement of a pressure dressing and a spinal drain to diminish the CSF pressure. Surgical exploration and repair of the dural defect may be necessary if the CSF leak does not resolve within 1 week. A middle ear effusion is often apparent after infratemporal skull base approaches because of dysfunction or interruption of the eustachian tube. Tympanostomy tubes are not placed for at least 6 weeks postoperatively, however, because there is always a risk of CSF communication.

We have encountered patients who developed profuse unilateral rhinorrhea in the postoperative period that was misinterpreted as a CSF leak. These cases all were associated with surgical dissection of the petrous ICA and are probably due to loss of the sympathetic fibers that travel along the ICA in their route to the nasal mucosa. This loss produces vasomotor rhinitis that may be treated with the use of anticholinergic nasal sprays. Testing of the fluid for β2-transferrin is mandatory, however, to rule out a CSF leak.

Cosmetic deformities may result from the loss of soft tissue and bone. Transposition of the temporalis muscle results in a depression in the temporal area. This depression can be lessened by placement of a free-fat graft or hydroxyapatite cement in a secondary surgery. If the temporalis muscle is not transposed, the anterior margin of the muscle should be resutured anteriorly and superiorly to prevent its retraction and a resulting depression lateral to the orbital rim. The use of microvascular free muscle flaps, such as the rectus abdominis flap, for reconstruction may necessitate sacrifice of the zygomatic arch to accommodate the additional bulk. As the muscle atrophies, significant depression may occur. It is important to repair all periosteal and muscle attachments around the maxilla, orbital rim, and zygomatic arch to avoid a “cadaveric” look that occurs when the soft tissues over these areas atrophy or retract. Large muscle flaps, such as a latissimus dorsi flap, may swell and compress the brain if the cranial base is not reconstructed.

REFERENCES

1. Barbosa J.F. Surgery of extensive cancer of paranasal sinuses: Presentation of a new technique. Arch Otolaryngol. 1961;73:129-138.

2. Terz J.J., Young H.F., Lawrence W.Jr. Combined craniofacial resection for locally advanced carcinoma of the head and neck, II: Carcinoma of the paranasal sinuses. Am J Surg. 1980;140:618-624.

3. Fisch U. The infratemporal fossa approach for the lateral skull base. Otolaryngol Clin North Am. 1984;17:513-552.

4. Biller H.F., Shugar J.M.A., Krespi Y.P. A new technique for wide-field exposure of the base of the skull. Arch Otolaryngol. 1981;107:698-707.

5. Sekhar L.N., Schramm V.L., Jones N.F. Subtemporal-preauricular infratemporal fossa approach to large lateral and posterior cranial base neoplasms. J Neurosurg. 1987;67:499.

6. Cocke E.W.Jr., Robertson J.H., Robertson J.T., Crooke J.P.Jr. The extended maxillotomy and subtotal maxillectomy for excision of skull base tumors. Arch Otolaryngol Head Neck Surg. 1990;116:92-104.

7. Janecka I.P., Sen C.N., Sekhar L.N., Arriaga M. Facial translocation: A new approach to the cranial base. Arch Otolaryngol Head Neck Surg. 1990;103:413-419.

8. Catalano P.J., Biller H.F. Extended osteoplastic maxillotomy: A versatile new procedure for wide access to the central skull base and infratemporal fossa. Arch Otolaryngol Head Neck Surg. 1993;119:394-400.

9. Snyderman C.H., Carrau R.L., de Vries E.J.. Carotid artery resection: Update on preoperative evaluation. Johnson J.T., Derkay C.S., Mandell-Brown M.K., Newman R.K., editors. AAO-HNS Instructional Courses, 6. 1993, 341-346.

10. Netterville J.L., Jackson G., Civantos F. Thyroplasty in the functional rehabilitation of neurotologic skull base surgery patients. Am J Otol. 1993;14:460-464.

11. Carrau R.L., Pou A., Eibling D.E., et al. Laryngeal framework surgery for the management of aspiration. Head Neck. 1999;21:139-145.

12. Pou A., Carrau R.L., Eibling D.E., Murry T. Laryngeal framework surgery for the management of aspiration in high vagal lesions. Am J Otolaryngol. 1998;19:1-8.

13. Nuss D.W., Janecka I.P., Sekhar L.N., Sen C.N. Craniofacial disassembly in the management of skull-base tumors. Otolaryngol Clin North Am. 1991;24:1465-1497.

14. Sekhar L.N., Sen C., Snyderman C.H., Janecka I.P. Anterior, anterolateral, and lateral approaches to extradural petroclival tumors. In: Sekhar L.N., Janecka I.P., editors. Surgery of Cranial Base Tumors. New York: Raven Press; 1993:157-223.