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Endoscopic Approaches to the Craniovertebral Junction
https://t.me/med1917
ET
ET
*
ET
a
SP
CD
S
b
c
d
Rt
ET
g i
Fig. 21.6 Stepwise demonstration of intraoperative endoscopic photographs. (a) A vertical incision was made on nasopharyngeal mucosa. ET, eustachian tube; S, suction tip; SP, soft palate. Asterisk, Bovie electrocautery. (b–e) The tumor (arrow) was removed in piecemeal with curved curette (pound signs). CD, clival dura. (f) Tumor erosion of the lower clivus was drilled (arrow head) and resected. (g) The angled endoscopes were used for visual confi rmation of radical resection of the tumor. (h) The operative space was packed with Gelfoam and fat graft, and was sealed with fi brin glue. (i) Endoscopic follow-up photograph taken after weeks of surgery demonstrated good healing and epithelialization of the operative wound (circle); Rt ET, right eustachian tube.
h
21.3 Common Pathologies of Craniovertebral Junction
The CVJ supports the cranial vault over the cervical spine and allows movements in sagittal, coronal, and axial planes in humans. The unique anatomic, developmental and biomechanical characteristics of CVJ are drastically different in humans than other quadrupedal vertebrae animals. Harboring the critical neural structure and functioning as one of the most mobile vertebral segments, the CVJ strikes a precise balance to achieve maximum
Fibrin glue
SP
mobility while maintaining reliable stability. Any deviation of functions or structures will lead to severe neurologic sequelae in this critical area. The pathologies in this area include developmental, rheumatological, traumatic, neoplastic, and infectious processes.
21.3.1 Developmental Anomalies
The CVJ has an unique embryonal development. The development of CVJ includes “pro-atlas” comprising of the fourth occipital sclerotome to form the tip of dens, dorsal cranial articulating facet, and occipital condyle.
fe
Rt
ET
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a b
e
Fig. 21.7 Serial images of a patient with severe deformity at the craniovertebral junction. (a–c) Preoperative sagittal view of T2W MRI (a) and sagittal (b) and axial (c) reformatted CT demonstrated severe bony deformity causing cord compression (arrows). (d–f) Postoperative CT including three-dimensional reformatted (d), sagittal (e), and axial (f) view demonstrated the extent of decompression after the fi rst-stage anterior transnasal transpharyngeal surgery. The patient was scheduled for posterior correction and fi xation but he declined the surgery.
The “primitive atlas” is derived from the cranial portion of the first cervical sclerotome and caudal portion of the fourth occipital sclerotome to form the lateral mass, pedicle, and lamina of the atlas and the remainder part of the odontoid process. The “primitive axis” is derived from the caudal portion of the first and cranial portion of the second cervical sclerotome and forms the body and posterior elements of C2 and the C2–C3 intervertebral disc.
14
Os odontoideum is a rare condition involving the presence of an ossicle with smooth circumferential cortical margins that has no osseous continuity with the vertebral body of C2. The clinical importance of this entity is that the attachment of transverse atlantal ligament (TAL) onto this mobile or incompetent ossicle jeopardizes the restraining effect of atlantoaxial motion and inflicts atlantoaxial instability. The etiology of os odontoideum remains controversial, with evidence supporting both acquired and congenital causes.
15
A similar but more common condition is ossiculum terminale, which means the nonunion of the dens tip at the secondary ossification center. Ossiculum terminale is typically distal to the attachment of TAL and thus theoretically does not cause atlantoaxial instability. However, certain cases can also have hypoplastic basal dental segments with short dental pivot, which may inflict atlantoaxial instability and high cervical cord compression.
14
Basilar invagination and basilar impression are uncommon conditions in which the superior part of the odontoid migrates upward into the foramen magnum. The terms basilar invagination and basilar impression are often used interchangeably to indicate the upwards migration of the upper cervical spine. Basilar invagination is defined as upward displacement of vertebral elements into the foramen magnum due to a developmental anomaly of the structures surrounding the foramen magnum. Alternatively, basilar impression typically refers to an upward displacement secondary to softening of bones at the base of the skull in certain pathologic conditions such as generalized osteopenia, osteomalacia, Paget’s disease, hyperparathyroidism, osteogenesis imperfecta, cretinism, achondroplasia, osteopetrosis, and mucopolysaccharidoses. Local bone destruction by neoplasm, infection or trauma is also included in basilar impression. “Cranial settling” is typically applied to CVJ changes associated with rheumatoid arthritis.
16
Goel proposed that basilar invagination is a result of chronic atlantoaxial instability and can best be addressed with segmental atlantoaxial fixation with facet arthrodesis.
17
Thus, the anterior transoral approach might not always be necessary. He classified facetal malalignments into three types. Type 1 means the facet of atlas is dislocated anterior (anterior slippage) to the facet of axis on lateral imaging. More often in cases with group A basilar invagination, such alignments are typically seen in mobile
c
fd
226
NS
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Endoscopic Approaches to the Craniovertebral Junction
OT
a
d
Rt ET
Rt ET
OT
DM
SP
AT
b
OT
e
c
Rt ET
f
SP
NS
g
Fig. 21.8 Stepwise demonstration of intraoperative endoscopic photographs. (a) A vertical mucosal incision was made directly on the nasopharyngeal wall. NS, nasal septum; Rt ET, right eustachian tube; SP, soft palate. (b) Anterior tubercle of C1 and the anteriorly displaced odontoid process were exposed. AT, C1 anterior tubercle; OT, odontoid tip of C2. (c–e) Bony structures’ compression of the spinal cord were drilled and removed. DM, dural matter; OT, odontoid tip. (f–g) The operative cavity was packed with Gelfoam and fat graft, and was sealed with fi brin glue. NS, nasal septum; Rt ET, right eustachian tube; SP, soft palate. (h–i) The lower part of the operative wound with fat graft (arrow) was visualized from a transoral angle of view. A suture stitch (arrow head) was made for xation of fat graft and approximation of wound. T, tongue.
and reducible atlantoaxial dislocations. The odontoid process is displaced posteriorly and superiorly, resulting in atlantoaxial dislocation as manifested by an increase in the atlantodental interval and basilar invagination. The odontoid process directly indents into the craniocervical cord and results in symptoms related to direct neural compression in a relatively acute fashion. Type 2 refers to posterior dislocation of atlas facets in relation to the facet of axis. Type
SP
h
i
T
3 is when the facets are in alignment and the instability is diagnosed on the basis of clinical and radiologic evidence and, more importantly, it is diagnosed by direct surgical manipulation during surgery. In types 2 and 3 atlantoaxial facetal dislocations, the atlantodental interval is not altered and the odontoid process does not directly indent into the neural structures. Types 2 and 3 facetal dislocations are more often associated with group B basilar invagination and
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b ca
d e f
Fig. 21.9 Comparison of pre- and postoperative images of a patient who underwent endoscopic trans-oral odontoidectomy. (a–c) Preoperative MRI (a) and CT (b and c) demonstrated severe deformity and spinal cord compression even after posterior decompressive surgery with intended fusion 3 months ago. The hard palate (arrow) was as high as the midclivus level, which precluded endoscopic transnasal odontoidectomy. (d–f) Postoperative MRI (d) and CT (e and f) demonstrated the extent of decompression.
cases with Chiari’s malformation and syringomyelia.18 The primary goal of treatment is realignment and segmental stabilization, best achieved with facet arthrodesis or posterior fixation. or suboccipital decompression is only needed in certain cases with severe or precipitating symptoms.
19
Transoral or transnasal decompression
21.3.2 Rheumatological, Traumatic, Neoplastic, and Other Disease Processes
Rheumatoid disease can cause bony and ligamentous destruction in CVJ most commonly presented as atlantoaxial instability (25% of rheumatoid arthritis patients), basilar invagination (8% of rheumatoid arthritis patients), and pannus formation around the odontoid. The pannus can produce collagenases and other proteolytic enzymes capable of destroying ligaments, tendons, cartilage, and bone in the joint. These damages potentially cause ligamentous laxity and bone erosions, which may lead to subluxation and instability. Subluxation also causes the anterior shift of the C1 arch and a decrease in the dimension of the spinal cannel by the posterior arch of the atlas. Anterior decompression is mandatory when ventral compression is significant. Reduction with
external traction is prudent prior to posterior fixation to achieve best surgical results.
The CVJ is vulnerable to trauma because of the large le­ver arm formed rostrally by the cranium and the relative high freedom of movement of the CVJ, which depends disproportionately on ligamentous structures rather than on intrinsic bony stability. Injuries disrupt the structur­al integrity, and vital damage to the spinal cord carries a high likelihood of death or severe neurologic sequelae. However, the traumatic condition of CVJ has a great vari­ety and therefore is beyond the scope of this chapter.
All types of neoplasm can arise in this area from os­seous structure or soft tissue surrounding this area. Osseous tumors include chordoma, chondrosarcoma, plasmacytoma, osteoblastoma, fibrous dysplasia, eo­sinophilic granuloma, metastatic tumor, and giant cell tumor. Extra-axial lesions include meningioma, neurinomas, paragangliomas, and glomus tumors, and less frequent are dermoid, teratomas, neurenteric cysts, and arachnoid cysts. unique pathologies at CVJ with their origin presum­ably from remnant notochord. These locally aggressive malignant tumors are most commonly located at the sphenooccipital and sacrococcygeal segments of the axial skeleton. In fact, 25 to 39% of chordomas arise at the clivus. complete tumor removal provides the best long-term
22
Most reports have indicated that radical or
21
Chordomas are uncommon but
20
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U
DM
OP
OP
T
a
b
c
U
d
Fig. 21.10 Stepwise demonstration of intraoperative photographs. (a) The uvula and soft palate were retracted superiorly, and a vertical incision was made on oropharyngeal mucosa. Two traction sutures (arrow) were done on both sides of the wound for better exposure. Most steps of the procedure were done under microscope but the upmost portion could only be approached with endoscope. T, tongue; U, uvula. (b, c) The anterior tubercle of C1 and odontoid process were drilled and removed. DM, dural matter; OP, odontoid process. (d–f) After decompression, the mucosal wound was sutured with several stitches. U, uvula.
outlook for survival; however, several factors influence such a resection, the optimal surgical approaches, the associated complications, and even the survival benefit achieved by such a resection, which remain controver­sial. The surgical approaches to skull base chordoma can be broadly classified as anterior midline approaches and lateral approaches. The anterior midline approaches include extended subfrontal, transmaxillary, trans­mandibular, endoscopic endonasal, transcervical, and
e
f
ligamentous laxity and instability and then the bone to cause destruction and collapse. It usually takes an insidious clinical course from months to years to produce symptoms characterized by cervicomedullary compression, cranial nerve deficits, atlantoaxial instability, and abscess forma-
27,28
tion.
The mainstay of treatment includes optimal anti­biotic coverage and surgical decompression/fixation if neu­rologic deterioration has developed and/or instability has occurred.
transoral approaches. The lateral approaches include frontotemporal orbitozygomatic, anterior transpetrosal, preauricular infratemporal, combined supra- and infra­tentorial transtemporal, and extreme lateral transcon-
22,23
dylar.
Selection of an approach must take into con­sideration the location of the main tumor bulk and its relation to the carotid, the vertebral and basilar arteries, the cavernous sinus, and the brainstem.
5
Other locally advanced metastatic tumors or malignancies arise from the local structure, such as nasopharyngeal carcinoma, while other head and neck cancers can also use these approaches to resect. As the approaches became more extensive, the techniques to reconstruct the skull base defects evolved simultaneously to minimize untoward complications, especially with CSF leakage.
24–26
An infectious process can involve the CVJ to cause liga­mentous destruction and instability. Take tuberculosis for instance; the primary infection is usually of a pulmonary or mediastinal lymph node and the disease progresses with lymphatic spread to the synovial lining of CVJ. Subse­quently, it extends to the surrounding ligaments to cause
21.4 Complications and Their Avoidance
There are many critical anatomic structures around the CVJ, including vascular and neural tissues. Injury of them could cause serious neurologic deficits or functional im­pairment. For example, injury to the brain stem, cranial nerves, or spinal cord could result in quadriparesis, re­spiratory failure, and aspiration. Injury to the vertebral artery, carotid artery, or basilar artery could also be prob­lematic and even fatal. This endoscopic surgery per se is minimally invasive to the CVJ and rarely causes velopha­ryngeal insufficiency or difficulty of phonation, as there are little alterations to the surrounding musculatures of the nasopharynx and the larynx. Persistent postopera­tive CSF leakage might eventually cause meningitis or encephalitis, although sometimes the CSF leakage would be self-limiting. Care must be taken to repair the dural incision, for example, with autologous fat and bone grafts
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for smaller defects or a nasoseptal mucosal flap for larg-
11
er.
Postoperative bed rest or CSF diversion (i.e., lumbar drainage) could also be beneficiary in cases of low-flow and low-pressure CSF leakage.
Surgical tips to avoid complications include thorough preoperative evaluations, use of intraoperative image guidance, meticulous dissection, and reconstruction. Preoperative thin-cut CT scans is extremely useful for de­piction of the bony anatomy around the CVJ. Moreover, CT angiography provides good knowledge of the course of major vessels of its neighborhood. During the opera­tion, identification of the midline is essential, and can be assisted by navigation system. For particular cases, it is an advantage to have intraoperative fluoroscopy at hand for real-time assessment of the cranial-caudal location as well as the extent of surgical field. The deeply seated tar­get of surgery can be visualized under the endoscope, and some lateral lesions can also be seen using angled endo­scopes. However, some of them may be difficult to reach with currently available instruments, even with those specially designed endoscopic tools. Furthermore, the endoscopic views are two-dimensional and there is in­evitably less tactile feedbacks when using the long-shaft surgical instruments. Therefore, meticulous dissection is warranted during surgery. Hemostasis could be more dif­ficult than traditional microsurgery, which is performed under three-dimensional microscopic visualization. Last but not least, efforts are necessary for repair of durotomy to minimize the chance to postoperative CSF leakage and subsequent infection of the central nervous system.
References
1. Agrawal A, Cavalcanti DD, Garcia-Gonzalez U, et al. Comparison of extraoral and transoral approaches to the craniocervical junc­tion: morphometric and quantitative analysis. World Neurosurg 2010;74(1):178–188
2. Enepekides DJ, Donald PJ. Transoral approaches to the clivus and nasopharynx. Otolaryngol Clin North Am 2001;34(6):1105–1121, ix
3. Hsu W, Wolinsky JP, Gokaslan ZL, Sciubba DM. Transoral approaches to the cervical spine. Neurosurgery 2010;66(3, Sup­pl):119–125
4. Menezes AH. Surgical approaches: postoperative care and compli­cations “transoral-transpalatopharyngeal approach to the cranio­cervical junction”. Childs Nerv Syst 2008;24(10):1187–1193
5. Dlouhy BJ, Dahdaleh NS, Menezes AH. Evolution of transoral approaches, endoscopic endonasal approaches, and reduction strategies for treatment of craniovertebral junction pathology: a treatment algorithm update. Neurosurg Focus 2015;38(4):E8
6. Moshel YA, Schwartz TH. Endoscopic transnasal versus transoral approaches to the craniovertebral junction. World Neurosurg 2010;74(6):568–569
7. Weissler MC. Transoral approaches to the skull base. Ear Nose Throat J 1991;70(9):587–592
8. El-Sayed IH, Wu JC, Ames CP, Balamurali G, Mummaneni PV. Combined transnasal and transoral endoscopic approaches to the craniovertebral junction. J Craniovertebr Junction Spine 2010;1(1):44–48
9. El-Sayed IH, Wu JC, Dhillon N, Ames CP, Mummaneni P. The im­portance of platybasia and the palatine line in patient selection for endonasal surgery of the craniocervical junction: a radiographic study of 12 patients. World Neurosurg 2011;76(1–2):183–188, discussion 74–78
10. Wu JC, Huang WC, Cheng H, et al. Endoscopic transnasal trans­clival odontoidectomy: a new approach to decompression: tech­nical case report. Neurosurgery 2008;63(1, Suppl 1):ONSE92-4, discussion E94
11. Yen YS, Chang PY, Huang WC, et al. Endoscopic transnasal odon­toidectomy without resection of nasal turbinates: clinical out­comes of 13 patients. J Neurosurg Spine 2014;21(6):929–937
12. Kuo CH, Yen YS, Wu JC, et al. Primary endoscopic transnasal trans­sphenoidal surgery for giant pituitary adenoma. World Neurosurg 2016;91:121–128
13. Kuo CH, Yen YS, Wu JC, Chen YC, Huang WC, Cheng H. Primary endoscopic transnasal transsphenoidal surgery for magnetic res­onance image-positive Cushing disease: outcomes of a series over 14 years. World Neurosurg 2015;84(3):772–779
14. Pang D, Thompson DN. Embryology and bony malformations of the craniovertebral junction. Childs Nerv Syst 2011;27(4):523–564
15. Rozzelle CJ, Aarabi B, Dhall SS, et al. Os odontoideum. Neurosur­gery 2013;72(Suppl 2):159–169
16. Smoker WR. Craniovertebral junction: normal anatomy, craniome­try, and congenital anomalies. Radiographics 1994;14(2):255–277
17. Goel A. Craniovertebral junction instability: a review of facts about facets. Asian Spine J 2015;9(4):636–644
18. Goel A. Basilar invagination, Chiari malformation, syringomyelia: a review. Neurol India 2009;57(3):235–246
19. Chang PY, Yen YS, Wu JC, et al. The importance of atlantoaxial fixa­tion after odontoidectomy. J Neurosurg Spine 2015;13:1–9
20. Colli B, Al-Mefty O. Chordomas of the craniocervical junc­tion: follow-up review and prognostic factors. J Neurosurg 2001;95(6):933–943
21. Menezes AH. Craniovertebral junction neoplasms in the pediatric population. Childs Nerv Syst 2008;24(10):1173–1186
22. Sen C, Triana AI, Berglind N, Godbold J, Shrivastava RK. Clival chor­domas: clinical management, results, and complications in 71 pa­tients. J Neurosurg 2010;113(5):1059–1071
23. Shidoh S, Toda M, Kawase T, et al. Transoral vs. endoscopic endona­sal approach for clival/upper cervical chordoma. Neurol Med Chir (Tokyo) 2014;54(12):991–998
24. Horowitz PM, DiNapoli V, Su SY, Raza SM. Complication avoid­ance in endoscopic skull base surgery. Otolaryngol Clin North Am 2016;49(1):227–235
25. Klatt-Cromwell CN, Thorp BD, Del Signore AG, Ebert CS, Ewend MG, Zanation AM. Reconstruction of skull base defects. Otolaryn­gol Clin North Am 2016;49(1):107–117
26. Tien DA, Stokken JK, Recinos PF, Woodard TD, Sindwani R. Com­prehensive postoperative management after endoscopic skull base surgery. Otolaryngol Clin North Am 2016;49(1):253–263
27. Qureshi MA, Afzal W, Khalique AB, Pasha IF, Aebi M. Tuberculosis of the craniovertebral junction. Eur Spine J 2013;22(Suppl 4):612–617
28. Suarez-Almazor ME, Russell AS. Anterior atlantoaxial subluxation in patients with spondyloarthropathies: association with peri pheral disease. J Rheumatol 1988;15(6):973–975
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Chapter 22
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22.1 Surgical Technique 232
The “Far Medial”
(Transcondylar/
Transtubercular)
Approach to the
Inferior Third
of the Clivus
22.2 Complications, Tips and Tricks 235
22.3 Case Example 235
22.4 Conclusion 235
The “Far Medial” (Transcondylar/Transtubercular) Approach to the Inferior Third of the Clivus
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22 The “Far Medial” (Transcondylar/Transtubercular) Approach to the Inferior Third of the Clivus
Martin Corsten, Srikant S. Chakravarthi, Juanita M. Celix, Sammy Khalili, Melanie Fukui, Richard Rovin, Amin Kassam
Introduction
The expanded endonasal approach (EEA) has been described as a minimally invasive approach to access le­sions of the anterior portion of the foramen magnum and inferior one-third of the clivus. clival tumors such as chordomas and chondrosarcomas, and tumors in the anterior foramen magnum (usually meningiomas). In addition, access via EEA to the odontoid process (for lesions such as basilar invagination, rheuma­toid pannus, odontoid fractures, and tumors) has been a tremendously successful approach. benefits of EEA in this setting is that the lateral or postero­lateral open approaches (e.g., far lateral, retrolabyrinthine presigmoid) require manipulation of the lower cranial nerves or the internal carotid artery (ICA) to gain access to the lesion; the direct medial-to-lateral approach of EEA obviates the need for this manipulation of critical neuro­vascular structures and avoids crossing the plane of the respective cranial nerves that are located posterolateral.
One significant limitation of the standard EEA ap­proach to the inferior third of the clivus is in the presence of lateral extension of the tumor along the occipital con­dyle beyond the hypoglossal canal. However, if the lesion is located medial to the hypoglossal canal, then the “far medial” approach affords access to these more medially placed tumors at the pontomedullary and cervicomedul­lary junction. divided into two compartments by the hypoglossal canal: (1) superiorly, the jugular tubercle, and (2) inferiorly, the occipital condyle. The transtubercular approach can be used to gain access to the jugular foramen, to biopsy or resect lesions such as schwannomas, paragangliomas, and meningiomas. Resection of the occipital condyle is more limited, as significant resection of the condyle can result in spinal instability. As a general rule, if one respects the plane of the hypoglossal canal, that is, does not cross this as the lateral limit, then it is much less likely to create instability as the majority of the condyle and atlanto­occipital (AO) joint capsule will be preserved. In addition, tumors in the hypoglossal canal proper can be biopsied
5,6
Anatomically, the lateral inferior clivus is
1,2
These lesions can include
3,4
One of the main
or excised through this “far medial” approach; in some cases, the etiology of these lesions may be unknown until they are exposed through EEA. Lesions such as schwan­nomas, hemangiomas, extramedullary plasmacytomas, and lymphomas may occur within the hypoglossal canal, requiring exposure for tissue diagnosis.
22.1 Surgical Technique
22.1.1 Step 1: Standard Exposure of the Nasopharynx
The transtubercular approach begins with the removal of the ipsilateral inferior turbinate. Typically, in endonasal skull base surgery, the right middle turbinate is removed to allow room for the endoscope, but in cases involv­ing the nasopharynx or clivus, the inferior turbinate is removed instead. A nasoseptal flap, if desired, is raised on the side contralateral to the tumor. A posterior septec­tomy is performed. The nasopharynx, torus tubarius, and Eustachian tube (ET) orifice are then visualized.
22.1.2 Step 2: Division of the Ipsilateral Eustachian Tube
The next maneuver is to enter the ipsilateral parapharyn­geal space and to mobilize the ET orifice medially (it will be resected en bloc with the nasopharyngeal mucosa). The en­doscopic scissors are inserted into the mucosa just lateral to the ET orifice, and oriented vertically at first and spread to dissect the parapharyngeal space and creating a window between the carotid and ET. A cut in this vertical direction at the level of the foramen lacerum would lacerate the pe­trous carotid artery. Therefore, the scissors are turned from a vertical to a horizontal plane, making them parallel to the plane of the horizontal carotid, and only then is the ET tran­sected. This rotation from a vertical to horizontal cannot be overemphasized to protect the ICA (Fig. 22.1).
ET
abc
Fig. 22.1 Avoiding the parapharyngeal carotid artery—vertical to horizontal transection. (a) The vertical position of the scissors along the parapharyngeal space. (b) Note the horizontal rotation of the upper blade of the scissors. (c) Eustachian tube and torus tubarius transected. ET, Eustachian tube; FL, foramen lacerum; P-ICA, petrous segment of internal carotid artery; TT, torus tubarius; VN, vidian nerve.
232
Meckel cave
VN
p-
FL
ICA
ET
FL
ET
P- ICA
TT
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22.1.3 Step 3: Nasopharyngectomy / Resection of the Basopharyngeal Fascia
Next, a nasopharyngectomy is performed. The mucosa at the superior aspect of the nasopharynx is transected with electrocautery, and the mucosa of the nasopharynx is removed. The nasopharyngeal mucosa is extreme­ly adherent to the underlying muscle, especially in the midline. As such, it is difficult to remove and a variety of strategies can be employed to remove this mucosa, including the use of cautery, Kerrison forceps, and/or the microdebrider. Once the nasopharyngeal mucosa is removed, the longus capitis muscle is exposed.
At this point, the basopharyngeal fascia needs to be divided. A wide sphenoidotomy is performed, and the palatovaginal canal is identified. The basopharyngeal fascia is continuous with the palatovaginal canal, and its attachment there is the most adherent. This attach­ment is divided with a Colorado tip electrocautery. It is critical to observe here that the basopharyngeal fascia is also continuous with the cartilaginous ring around the carotid artery at the foramen lacerum, so division of this fascia requires attention to avoid injuring the artery. The division of the basopharyngeal fascia exposes the carotid artery and foramen lacerum (Fig. 22.2).
22.1.4 Step 4: Completion of Resection of the Vomer
The next step is to complete the removal of the vomer. The caudal aspect of the vomer has been removed with the posterior septectomy, and the cranial aspect can now be removed en bloc by passing the drill through the palatovaginal canal bilaterally, then drilling inferior and superior to the vomer, and fracturing it off laterally. The removal of the vomer further exposes the longus capitis, which is removed in a fashion similar to that of the nasopharyngeal mucosa removal, with a variety of instruments including cautery, Kerrison forceps, and the microdebrider (Fig. 22.3).
Meckel
cave
Fig. 22.2 Resection of the basopharyngeal fascia. ET, Eustachian tube; TT, torus tubarius; V, vomer; VN, vidian nerve.
S P
A
MP
Fig. 22.3 Removal of vomer and exposure of longus capitis muscle. ET, Eustachian tube; FL, foramen lacerum; ICA, internal carotid artery; LC, longus capitis; MP, medial pterygoid; PVC, palatovaginal canal; SPA, sphenopalatine artery; V, vomer; VN, vidian nerve.
VN
V
ETTT
ET
Nasopharynx
ICA
VN
FL
VPVC
LC
ET transected
VN
22.1.5 Step 5: Identifi cation of the Ipsilateral Medial Pterygoid Plate
The identification of the medial pterygoid is the next step. An endoscopic medial maxillectomy is performed, the extent of which depends on the nature of the lesion being exposed (more lateral extension requires more caudal resection of the lateral nasal wall). The mucosa over the medial pterygoid plate is then stripped away; the inferior turbinate artery will often bleed and require cautery during this step. The descending palatine and greater palatine arteries are identified at this time and mobilized laterally. The medial pterygoid plate, once exposed, is removed with high-speed drill; this step is critical to achieve lateral visualization (Fig. 22.4). The removal of the medial pterygoid allows identification of the medial pterygoid muscle.
MP
*
Fig. 22.4 Identifi cation of ipsilateral medial pterygoid muscle (MP). The medial pterygoid muscle will be subsequently stripped away to allow access to the transcondylar window. Starred (*) symbol indicates the location of the descending and greater palatine nerve and artery complex. ET, Eustachian tube; IT, inferior turbinate; LC, longus capitis; VN, vidian nerve.
LC
ET transected
ET
IT
233
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22.1.6 Step 6: Transection of the Parapharyngeal Muscles
The next step is the transection of the parapharyngeal muscles. The fossa of Rosenmüller is identified, and the tensor veli palatini muscle is identified and divided. This muscle’s origin is at the base of the medial pterygoid; it passes through the pterygoid hamulus and inserts into the contralateral tensor veli palatini muscle in the pala­tine aponeurosis. The remaining fibers of the longus capi­tis muscles as they insert into the lower third of the clivus and the AO joint are then removed; this exposes the AO membrane. Deep to the AO membrane is the apical liga­ment, whereas lateral to it is the alar ligament (Fig. 22.5).
Fig. 22.5 Transection of parapharyngeal muscles, exposure of atlanto-occipital membrane (AOM).
AOM
22.1.7 Step 7: Resection of Remaining Inferior One-third of Clivus
A focal resection of the bone of the inferior one-third of the clivus is then undertaken, to expose the occipital condyle. As mentioned previously, the hypoglossal canal divides the inferior lateral clivus into two portions: the jugular tubercle superiorly and the occipital condyle in­feriorly. The hypoglossal canal then continues obliquely, dividing the condyle into medial and lateral components. The supracondylar groove represents a good anatomic landmark at this time for the hypoglossal canal (Fig. 22.6).
22.1.8 Step 8: Tailored to Lesion
SG
OC
Fig. 22.6 Resection of inferior one-third of clivus, exposure of supracondylar groove (SG). BF, basopharyngeal fascia; ET, Eustachian tube; IT, inferior turbinate; OC, occipital condyle.
BF
Being Resected
The resection from this point is dependent on the nature of the lesion being resected or biopsied. Lesions within the hypoglossal canal can be exposed through judicious and targeted drilling at the supracondylar groove continu­ing inferomedially, with significant use of image guidance to direct the operator to the exact location of the canal. The anteromedial aspect of the hypoglossal canal can be drilled away with impunity, allowing for biopsies of tis­sue within the canal or decompression of the nerve in the canal. However, it is critical not to drill away the bone at the posterolateral aspect of the hypoglossal canal, as this will result in the removal of more than one-half of the occipital condyle and result in spinal instability at the AO
7
More importantly, this often requires disruption of
joint. the synovial joint of the articular facet of C1 and condyle, further predisposing the patient to instability.
Resection of the ventromedial aspect of the occipital condyle (taking care to preserve at least one-half of the condyle and synovial joint capsule, as described earlier) creates an endonasal ventromedial corridor with lateral extension that gives access to the vertebral artery at its insertion into the posterior cranial fossa. We have used this approach to secure and place a temporary clip on the vertebral artery extradurally to control a large intradural vertebrobasilar junction aneurysm.
Meanwhile, the superolateral limit of the tubercular compartment is the medial aspect of the jugular foramen.
8
OC
*
Fig. 22.7 Removal of tubercular compartment and exposure of CN IX, X, and XI. Starred symbol (*) indicates location of superior articular facet of C1. ET, Eustachian tube; OC, occipital condyle.
This tubercular compartment can be drilled away, limited by the inferior petrosal sinus superior and lateral and the hypoglossal nerve inferiorly. As the tubercular compartment is removed, the nerves of the jugular foramen (IX, X, XI) are exposed (Fig. 22.7). Access to the medial jugular foramen may be required to biopsy or debulk and decompress lesions in this area.
Dura
Foramen magnum
baslon
ET
IT
ET
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