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. 2013 Jan 30;5:21–24. doi: 10.2147/CMAR.S38768

Endoscopic endonasal approach for the treatment of a large clival giant cell tumor complicated by an intraoperative internal carotid artery rupture

Maurizio Iacoangeli 1,, Alessandro Di Rienzo 1, Massimo Re 2, Lorenzo Alvaro 1, Niccolò Nocchi 1, Maurizio Gladi 1, Maurizio De Nicola 3, Massimo Scerrati 1
PMCID: PMC3565560  PMID: 23403482

Abstract

Giant cell tumors (GCTs) are primary bone neoplasms that rarely involve the skull base. These lesions are usually locally aggressive and require complete removal, including the surrounding apparently healthy bone, to provide the best chance of cure. GCTs, as well as other lesions located in the clivus, can nowadays be treated by a minimally invasive fully endoscopic extended endonasal approach. This approach ensures a more direct route to the craniovertebral junction than other possible approaches (transfacial, extended lateral, and posterolateral approaches). The case reported is a clival GCT operated on by an extended endonasal approach that provides another contribution on how to address one of the most feared complications attributed to this approach: a massive bleed due to an internal carotid artery injury.

Keywords: clival giant cell tumor, endoscopic endonasal approach, internal carotid artery injury, minimally invasive surgery

Background

Giant cell tumors (GCTs) are primary bone lesions that usually involve the metaphyseal region of long bones in the appendicular skeleton. Although classified as benign entities, they can be locally aggressive and metastasize distant to the primary site of origin.1,2 Cranial lesions are rare and usually arise from the skull base rather than the vault.37 Due to the small number of skull base GCTs reported in the literature, recommendations on treating this type of lesion are still unclear, and the role of surgery, as well as adjuvant therapies, remains undefined.810 Complete tumor removal and drilling of the surrounding apparently healthy bone are preferable in order for patients to expect a complete clinical cure and a reduced recurrence rate, even though this approach implies a higher risk of intraoperative complications and neurologic impairments.

Historically performed through challenging open approaches, treatment of lesions located in the craniovertebral junction (CVJ) can nowadays be reached by less invasive procedures, such as the endoscopic extended endonasal approach (EEA).1114 We report a case of a clival GCT completely resected by a fully endoscopic EEA but complicated by an intraoperative tearing of the internal carotid artery (ICA). Injury to the ICA during endonasal surgery is the most feared and catastrophic complication that could happen during an EEA, and control of the surgical field is very challenging.1519

A review of the literature demonstrates that there is a lack of information with regard to the appropriate techniques and protocols in managing an ICA injury during endonasal surgery. This paper describes how to remove even large clival GCTs with adequate bony margins and how we treated the ICA injury.

Case presentation

A 31-year-old male was admitted to our hospital because of progressive headache and diplopia. Neurologic and vision examination revealed a right sixth cranial nerve palsy and double vision in the right lateral view only. Other cranial nerves were normal, as were visual field and acuity. The patient was fully cooperative and orientated without motor or sensory deficits, cerebellar tests were performed correctly, and the general state of his health was good. Brain magnetic resonance imaging and an angio-computed tomography scan showed a large osseous extradural lesion originating from the clivus, compressing both cavernous sinuses, and expanding into the nasal cavity and sphenoid sinus with erosion of the sellar floor. The ICAs were lateralized and upward dislocated, the dural layer was respected, and the brainstem was not compressed (Figure 1). Laboratory tests and chest X-ray were normal.

Figure 1.

Figure 1

Sagittal, axial, and coronal magnetic resonance images showing a large giant cell tumor originating from the clivus and involving both cavernous sinuses.

The patient was operated on by a fully endoscopic neuro-navigation guided EEA. The lesion was completely removed, but during the drilling of the surrounding healthy bone there was a little tearing of the left ICA. Local control of the bleeding was challenging, but it was obtained by using topic hemostatic agents and leaving microcottonoids adhering to the artery fissuration (Figure 2). An insufflate balloon catheter for nasal tamponade was put into the nasal cavity. The intraoperative tearing of the ICA led us to perform an immediate postoperative angiography, disclosing a pseudoaneurysm originating near the inferior meningohypophyseal trunk, which was successfully treated by embolization with coils (Figure 3).

Figure 2.

Figure 2

Endoscopic intraoperative images showing the erosion of the sphenoid bone by the tumor (A), the drilling of the apparently healthy bone near the carotid region (B), and the microcottonoid adhering to the artery fissuration (C).

Figure 3.

Figure 3

(A) Internal carotid artery angiography demonstrating the pseudoaneurysm originating near the inferior meningohypophyseal trunk and the microcottonoid adhering to the internal carotid artery fissuration (white asterisk). (B) Exclusion of the pseudoaneurysm after the endovascular treatment.

After 2 days of intensive care unit stay the patient was transferred to our department, showing progressive recovery of his neurologic status associated with a sharp improvement in the diplopia. The nasal tamponade was removed 4 days after surgery, and no bleeding was observed coming out from the nasal cavity. The patient was dismissed and sent home 1 week later.

Histologic evaluation of surgical specimens revealed the aspect of a GCT with no infiltration of the surrounding bone. Radiation therapy was not performed. Brain magnetic resonance imaging with angiographic sequences was done regularly 3, 6, and 12 months after surgery in the first year, every 6 months for a further 2 years, then annually.

Six years after surgery the patient was asymptomatic and did not present any relapse of the disease, and there were no signs of microcottonoid infection or aneurysm repermeabilization (Figure 4).

Figure 4.

Figure 4

Brain magnetic resonance imaging performed 6 years after surgery, demonstrating the absence of tumor relapse and no foreign body granuloma formation.

Discussion

GCTs are uncommon entities comprising 3%–7% of all primary bone neoplasms.20 They commonly originate in the epiphysis of long bones such as the distal femur, proximal tibia, and distal radius, and are rare in the cranium.21 Although they are infrequent, cranial GCTs have the tendency to involve the skull base, particularly the sphenoid and petrous temporal bone.6,7 Although treatment for typical GCT of the long bones is generally well defined, managing lesions located in the skull remains unclear, though a wide surgical excision is generally preferred in order to reduce the risk of local recurrence.8,9 Complete surgical removal of neoplasms originating in the clivus represents a challenge for the neurosurgeon, particularly when facing GCTs that also require the resection of the surrounding apparently healthy bone.22 Access to the clivus has traditionally necessitated extended lateral, posterolateral, and anterior surgical approaches. Lateral transtemporal or far lateral approaches require handling of the cranial nerve, as well as carotid and vertebrobasilar structures, to reach the clivus, thereby increasing the risk of their injury. Anterior approaches allow more direct access to the clivus, representing a preferable route, as they place the pathology at the center of the surgical field while leaving neurovascular structures peripherally. However, the transfacial approach is cosmetically disfiguring, and the sublabial or endonasal microscopic approach provides a narrow corridor that limits the view of the microscope, especially around the corner.23

Recently, advances in the endoscopic instrumentation have led to an increased use of endoscopic EEA to approach the CVJ.1114,23 Advantages of EEA include the utilization of natural apertures and corridors, improved visualization and magnification by moving the lens and by using a light source closer to the pathology, the possibility to look laterally with angled endoscopes, and the ability to approach the clivus without manipulating critical neurovascular structures, going straight to the tumor’s implant.

In this paper we report a case of GCT treated by an endoscopic EEA in which the close-up vision provided by the endoscope allowed us to completely remove the lesion and adequately drill the surrounding apparently healthy bone. This approach also permitted control of an intraoperative bleed due to an accidental tear of the left ICA. Injury of the ICA during endonasal surgery is a rare complication, but when it happens it can be fatal. Immediate packing or tamponade insertion is necessary to arrest the bleeding, and once the circulation is stabilized the patient should undergo ICA angiography to disclose and treat the ICA injury.1519 Darkening of the surgical field as a result of blood dirtying the endoscope, as well as difficulties in quickly introducing hemostatic agents, are factors that make intraoperative bleeding control much more difficult in endoscopic endonasal surgery than in other open approaches.24 However, there are some tips and tricks to arrest the blood loss and, at the same time, continue the tumor excision.

In the case described here we found very useful the perfect collaboration between the two surgeons, the careful selection of the most appropriate nostril for endoscope positioning, the large bore suction placement, and the quick “blind” approach to the ICA rupture irrespective of the blood loss. Only once the surgical field was controlled was the site of bleeding addressed and the packing of the ICA tear done with the help of topical hemostatic agents and microcottonoids left adherent to the artery fissuration. This allowed temporary control of the bleeding, giving time for the definitive endovascular treatment, which was performed immediately after endonasal surgery.

Conclusion

Clival GCTs are very rare lesions that can now be completely removed by a minimally invasive, fully endoscopic EEA. The close-up vision provided by the endoscope facilitates complete removal of the tumor and surrounding bone, but at the same time it could be associated with challenging control of bleeding in case of ICA injury. A significant amount of experience, coordination, and teamwork by surgeons as well as some surgical tricks are needed to maintain a surgical view and arrest blood loss.

Footnotes

Disclosure

The authors report no conflicts of interest in this work.

References

  • 1.Siebenrock KA, Unni KK, Rock MG. Giant-cell tumour of bone metastasising to the lungs. A long-term follow-up. J Bone Joint Surg Br. 1998;80(1):43–47. doi: 10.1302/0301-620x.80b1.7875. [DOI] [PubMed] [Google Scholar]
  • 2.van Hoeven KH, Kellogg K, Bavaria JE. Pulmonary metastasis from histologically benign giant cell tumor of bone. Report of a case diagnosed by fine needle aspiration cytology. Acta Cytol. 1994;38(3):410–414. [PubMed] [Google Scholar]
  • 3.Zorlu F, Selek U, Soylemezoglu F, Oge K. Malignant giant cell tumor of the skull base originating from clivus and sphenoid bone. J Neurooncol. 2006;76(2):149–152. doi: 10.1007/s11060-005-4343-5. [DOI] [PubMed] [Google Scholar]
  • 4.Wolfe JT, 3rd, Scheithauer BW, Dahlin DC. Giant-cell tumor of the sphenoid bone. Review of 10 cases. J Neurosurg. 1983;59(2):322–327. doi: 10.3171/jns.1983.59.2.0322. [DOI] [PubMed] [Google Scholar]
  • 5.Watkins LD, Uttley D, Archer DJ, Wilkins P, Plowman N. Giant cell tumors of the sphenoid bone. Neurosurgery. 1992;30(4):576–581. doi: 10.1227/00006123-199204000-00017. [DOI] [PubMed] [Google Scholar]
  • 6.Motomochi M, Handa Y, Makita Y, Hashi K. Giant cell tumor of the skull. Surg Neurol. 1985;23(1):25–30. doi: 10.1016/0090-3019(85)90155-7. [DOI] [PubMed] [Google Scholar]
  • 7.Rock JP, Mahmood A, Cramer HB. Giant cell tumor of the skull base. Am J Otol. 1994;15(2):268–272. [PubMed] [Google Scholar]
  • 8.Manaster BJ, Doyle AJ. Giant cell tumors of bone. Radiol Clin North Am. 1993;31(2):299–323. [PubMed] [Google Scholar]
  • 9.Yamamoto M, Fukushima T, Sakamoto S, Tomonaga M. Giant cell tumor of the sphenoid bone: long-term follow-up of two cases after chemotherapy. Surg Neurol. 1998;49(5):547–552. doi: 10.1016/s0090-3019(97)00219-x. [DOI] [PubMed] [Google Scholar]
  • 10.Bennett CJ, Jr, Marcus RB, Jr, Million RR, Enneking WF. Radiation therapy for giant cell tumor of bone. Int J Radiat Oncol Biol Phys. 1993;26(2):299–304. doi: 10.1016/0360-3016(93)90210-m. [DOI] [PubMed] [Google Scholar]
  • 11.Abuzayed B, Tanriover N, Gazioglu N, Akar Z. Extended endoscopic endonasal approach to the clival region. J Craniofac Surg. 2010;21(1):245–251. doi: 10.1097/SCS.0b013e3181c5a294. [DOI] [PubMed] [Google Scholar]
  • 12.Arbolay OL, González JG, González RH, Gálvez YH. Extended endoscopic endonasal approach to the skull base. Minim Invasive Neurosurg. 2009;52(3):114–118. doi: 10.1055/s-0028-1119414. [DOI] [PubMed] [Google Scholar]
  • 13.Gladi M, Iacoangeli M, Specchia N, et al. Endoscopic transnasal odontoid resection to decompress the bulbo-medullary junction: a reliable anterior minimally invasive technique without posterior fusion. Eur Spine J. 2012;21( Suppl 1):S55–S60. doi: 10.1007/s00586-012-2220-4. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 14.Iacoangeli M, Di Rienzo A, Alvaro L, Scerrati M. Fully endoscopic endonasal anterior C1 arch reconstruction as a function preserving surgical option for unstable atlas fractures. Acta Neurochir (Wien) 2012;154(10):1825–1826. doi: 10.1007/s00701-012-1471-5. [DOI] [PubMed] [Google Scholar]
  • 15.Valentine R, Wormald PJ. Carotid artery injury after endonasal surgery. Otolaryngol Clin North Am. 2011;44(5):1059–1079. doi: 10.1016/j.otc.2011.06.009. [DOI] [PubMed] [Google Scholar]
  • 16.Solares CA, Ong YK, Carrau RL, et al. Prevention and management of vascular injuries in endoscopic surgery of the sinonasal tract and skull base. Otolaryngol Clin North Am. 2010;43(4):817–825. doi: 10.1016/j.otc.2010.04.008. [DOI] [PubMed] [Google Scholar]
  • 17.Valentine R, Wormald PJ. Controlling the surgical field during a large endoscopic vascular injury. Laryngoscope. 2011;121(3):562–566. doi: 10.1002/lary.21361. [DOI] [PubMed] [Google Scholar]
  • 18.Valentine R, Wormald PJ. A vascular catastrophe during endonasal surgery: an endoscopic sheep model. Skull Base. 2011;21(2):109–114. doi: 10.1055/s-0031-1275255. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 19.Park YS, Jung JY, Ahn JY, Kim DJ, Kim SH. Emergency endovascular stent graft and coil placement for internal carotid artery injury during transsphenoidal surgery. Surg Neurol. 2009;72(6):741–746. doi: 10.1016/j.surneu.2009.05.003. [DOI] [PubMed] [Google Scholar]
  • 20.Epstein N, Whelan M, Reed D, Aleksic S. Giant cell tumor of the skull: a report of two cases. Neurosurgery. 1982;11(2):263–267. doi: 10.1227/00006123-198208000-00012. [DOI] [PubMed] [Google Scholar]
  • 21.Goldenberg RR, Campbell CJ, Bonfiglio M. Giant-cell tumor of bone. An analysis of two hundred and eighteen cases. J Bone Joint Surg Am. 1970;52(4):619–664. [PubMed] [Google Scholar]
  • 22.Bitoh S, Takimoto N, Nakagawa H, Namba J, Sakaki S, Gohma T. Giant cell tumor of the skull. Surg Neurol. 1978;9(3):185–188. [PubMed] [Google Scholar]
  • 23.Fraser JF, Nyquist GG, Moore N, Anand VK, Schwartz TH. Endoscopic endonasal minimal access approach to the clivus: case series and technical nuances. Neurosurgery. 2010;67(3 Suppl operative):ons150–ons158. doi: 10.1227/01.NEU.0000383130.80179.41. [DOI] [PubMed] [Google Scholar]
  • 24.Kassam A, Snyderman CH, Carrau RL, Gardner P, Mintz A. Endoneurosurgical hemostasis techniques: lessons learned from 400 cases. Neurosurg Focus. 2005;19(1):E7. [PubMed] [Google Scholar]

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