▪ There are two ways to approach and perform a sphenoidotomy: transnasal and transethmoid.
▪ In the transnasal approach, the sphenoidotomy is performed while sparing the ethmoid cavity. Dissection proceeds medial to the middle turbinate. Common indications for this approach are isolated pathologic processes within the sphenoid sinus (e.g., fungal ball, isolated sphenoid sinusitis). This approach may also be combined with a posterior septectomy for an endoscopic transnasal approach to the pituitary sella (see Chapter 28).
▪ In the transethmoid approach, the uncinate process and inferior ethmoid air cells are removed to access the anterior face of the sphenoid sinus. This technique may be used in cases of isolated sphenoid disease, but most commonly is performed as a component of a complete functional endoscopic sinus surgery.
Anatomy
Sphenoid
▪ The sphenoid sinus has the following borders (Fig. 8.1):
– Anterior: superior turbinate and posterior ethmoid cells
– Lateral: cavernous sinus, optic nerve, and infratemporal fossae
– Superior: planum sphenoidale, anterior skull base
▪ The natural os of the sphenoid sinus lies in the medial and inferior portion of the sphenoid face, nearly always medial and posterior to the superior turbinate (Fig. 8.2).
Onodi Cell
▪ An Onodi cell is a posterior ethmoid cell that lies superior or lateral to the sphenoid sinus.
▪ When a sphenoidotomy is performed, it is crucial not to confuse the posterior wall of an Onodi cell with the anterior face of the sphenoid.
▪ A common cause of optic nerve or orbital apex injury in the early days of functional endoscopic sinus surgery was dissection through the posterior wall of an Onodi cell because it was mistaken for the anterior face of the sphenoid sinus (Fig. 8.3).
Vasculature
▪ The septal branch of the sphenopalatine artery runs horizontally along the inferior and anterior face of the sphenoid sinus.
Preoperative Considerations
▪ When a sphenoidotomy is performed, a greater palatine or sphenopalatine artery injection can be helpful in controlling intraoperative bleeding.
▪ A greater palatine artery injection is performed through the mouth. The greater palatine canal is in the hard palate, opposite the second molar. Bend the needle at 1.5 to 2 cm from the tip at a 45-degree angle, aspirate, and then inject 1 to 2 mL of 1% lidocaine with 1:100,000 epinephrine.
▪ A sphenopalatine artery injection can be performed transnasally. Identify the inferior attachment of the middle turbinate to the lateral nasal wall and inject roughly 1 mL of 1% lidocaine with 1:100,000 epinephrine 1 cm above the inferior border.
Fig. 8.1 Schematic drawings of the sphenoid sinus showing sagittal (A) and axial (B) views of the structures involved in a sphenoidotomy (shaded area).
Fig. 8.2 Axial CT scan showing the position of the natural sphenoid os medial, posterior, and inferior to the superior turbinate.
Radiographic Considerations
▪ The axial, coronal, and sagittal computed tomography (CT) scans are helpful to understand the anatomy.
▪ Identify the size and pneumatization of the sphenoid sinus.
▪ Look at the nature of the bone of the sphenoid walls. Fungal balls or long-standing inflammatory disease often results in thickened bone of the anterior face (sometimes requiring a drill for sphenoidotomy enlargement).
▪ Identify the presence of any Onodi cells.
▪ Identify the intersinus septum and track its path back to the posterior wall. Beware of any attachments to the internal carotid artery. If such an attachment is identified, it is advisable to avoid aggressive manipulation of the intersinus septum for fear of injuring the artery (Fig. 8.4).
Instrumentation
▪ 30- or 70-degree endoscope if the lateral or inferior portion of the sinus must be examined
▪ Straight microdébrider
▪ Straight sphenoid punch
▪ 45-degree through-cutting instrument
▪ J-curette
▪ 2- and 4-mm Kerrison rongeurs
Pearls and Potential Pitfalls
▪ Avoid operating in a narrow space when entering the sphenoid. Visualization is significantly improved by removing superior ethmoid air cells, which allows greater access to light from the endoscope.
Fig. 8.3 Coronal CT scans (A and B) revealing left Onodi cells. Note the location of the optic nerve in the roof of these cells.
Fig. 8.4 Axial CT scan showing a left intersinus septum leading to the carotid artery.
▪ A reliable method to identify the natural os of the sphenoid is to truncate the lower half of the superior turbinate. Avoid excising too much of the superior turbinate, because olfactory fibers are located in its most superior portion.
▪ Dissect from “known to unknown.” Identify the natural os first and then expand the antrostomy laterally.
▪ If image guidance is available, estimate the height of the septal branch of the sphenopalatine artery. This can be done by looking at the axial computed tomography (CT) sections and noting the location of the sphenopalatine foramen.
▪ Identify the presence of an Onodi cell preoperatively as well as intraoperatively. Mistaking the anterior surface of an Onodi cell for the sphenoid face can result in inadvertent injury to the orbital apex (Fig. 8.5).
▪ Avoid stripping mucosa off the skull base or medial orbital wall. This will often lead to prolonged localized postoperative mucosal edema and long-term neo-osteogenesis.
Surgical Procedures
Transnasal Sphenoidotomy
Step 1
▪ With a 0-degree endoscope, gently lateralize the middle turbinate to identify the lower half of the superior turbinate.
▪ Use a straight through-cutter to excise the lower half of the superior turbinate. This is done to identify the natural os of the sphenoid sinus (Fig. 8.6).
Step 2
▪ Enter the natural os with a J-curette and then dilate the os by fracturing the anterior sphenoid face in a lateral direction. Remove bony fragments.
▪ The sphenoid antrostomy can be enlarged with a Kerrison punch or straight mushroom punch.
Fig. 8.5 Computed CT (A) and (B) artist depiction showing the right Onodi cell in relation to the optic nerve. n., Nerve.
Fig. 8.6 Endoscopic view of the right sphenoethmoid recess. In a direction medial to the right middle turbinate, the natural os of the sphenoid sinus (asterisk) is visible posterior and medial to the superior turbinate.
Fig. 8.7 Endoscopic view of the left superior turbinate (identified with the suction device) after the basal lamellae have been removed and a posterior ethmoidectomy has been performed. BL, Basal lamella; M, maxillary sinus; PE, posterior ethmoid.
Transethmoid Sphenoidotomy
Dilation of the Natural Os
▪ After a posterior ethmoidectomy has been performed, identify the superior turbinate and its horizontal lamellae (Fig. 8.7).
Fig. 8.8 Endoscopic view of resection of the left superior turbinate with straight through-cutter forceps to allow visualization of the anterior sphenoid face.
▪ Remove the lower half of the superior turbinate to identify and then enlarge the natural os (Fig. 8.8). It is safest to find the os in its medial location and then, using a J-curette, fracture the anterior sphenoid face in a lateral direction.
▪ Enlarge the antrostomy by using an upbiting through-cutting instrument, Kerrison rongeur, or straight mushroom punch (Fig. 8.9).
▪ The “Bolger box” method is a technique for performing a sphenoidotomy without finding or resecting the superior turbinate.
▪ Draw a rectangular box with the borders being the superior turbinate medially, superior turbinate lamellae inferiorly, skull base superiorly, and orbit laterally. Draw a diagonal line through the box and enter the sphenoid face medial and inferior to the line (Fig. 8.11).
Special Considerations—Onodi Cell
▪ An Onodi cell lies superior to the natural os of the sphenoid sinus. Continued dissection through the posterior wall of an Onodi cell results in intracranial or orbital apex injury.
▪ The floor of an Onodi cell may be removed to create one continuous sphenoid cavity (Fig. 8.12).
Fig. 8.9 Endoscopic view (A and B) of the widening of the antrostomy (asterisk).
Fig. 8.10 Endoscopic view of the final antrostomy.
Fig. 8.11 Artist’s depiction of the Bolger box in endoscopic view. The box is a parallelogram bounded by the medial orbital wall laterally, basal lamella of the superior turbinate inferiorly, superior turbinate (ST) medially, and ethmoid roof (ER) superiorly. The natural sphenoid os is indicated by the red dot.
Fig. 8.12 Endoscopic view of a left-sided Onodi cell with the inferior floor removed (A), which creates one continuous sphenoid cavity (B).