Introduction
Skull base tumors are challenging, hard to access, and associated with high morbimortality.
Endonasal endoscopic approaches, in selected cases, offer advantages over transcranial
access, such as direct lesion access without the need for brain retraction, early
devascularization of the tumor, removal of invaded bone and dura-mater, and better
illumination and visualization of the surgical field.[[1]],[[2]],[[3]],[[4]],[[5]],[[6]]
The rise in popularity of endoscopic skull base surgery, together with the advent
of the nasoseptal flap, has drastically reduced rates of cerebrospinal fluid (CSF)
leakage, characterizing this surgical technique as revolutionary.[[7]],[[8]] Kassam et al.[[2]],[[3]],[[4]] carried out a systematization of the endoscopic expanded endonasal approach (EEA)
[[Figure 1]].
Figure 1: Illustration depicting sagital plane of skull base, divided into areas of endoscopic
approach. (A) transfrontal; (B) transcribriform: (C) transplanal; (D) transtuberculum;
(E) transellar; (F) transclival: (G) transodontoid. Transplanal and transtuberculum
region highlighted in Green. Source: Angelo Shuman/Ricardo Dolci (2018)
Transplanum and transtuberculum EEAs allow minimally-invasive, highly effective tumor
resection. However, a large bone and dural defect is created during the surgical procedure,
often associated with high-flow intraoperative CSF leaks [[9]] while posing a risk of postoperative CSF leakage.
Closure of the endoscopic craniectomy must be performed with care by isolating the
intracranial compartment from the sinonasal compartment, where the nasoseptal flap
plays a key role in this separation.[[7]],[[10]],[[11]] Closure can be carried out in multiple layers, using heterologous materials (dura-mater
substitutes, bovine collagen sponges, oxidized cellulose meshes, fibrin sealant) or
autologous materials (fat, nonvascularized flaps, microsurgical flaps with vascular
anastomosis, pedicled flaps or muscle tissue).[[10]],[[12]],[[13]]
In the present study, we describe the surgical technique employing autologous material
in two layers for skull base repair in patients submitted to endonasal endoscopic
resection of planum sphenoidale or tuberculum sellae meningiomas using nasoseptal
flap (onlay) and fascia lata (inlay). Associated complications were also investigated.
Methods
A retrospective study was conducted based on the review of patient medical records
and data collection after approval of the local Research Ethics Committee (permit
CAEE-08113819.7.0000.5479). The study inclusion criteria were:
-
Patients aged >18 years of both genders;
-
Magnetic resonance imaging (MRI)-confirmed diagnosis of planum sphenoidal or tuberculum
sela meningioma;
-
Patients submitted to endoscopic endonasal resection as a sole or initial treatment
between June 2013 and August 2018;
-
Intraoperative closure of skull base with the combined use of fáscia lata inlay and
nasoseptal flap onlay.
The study exclusion criteria were:
-
Patients classed as vulnerable (prisoners and pregnant women);
-
Pediatric patients.
All patients were submitted to the surgical procedure by the institution's skull base
team. All complications described in medical records were collected for up to 1 year
after the surgery.
Within the first 24 h of surgery, patients underwent computed tomography (CT) scan
of the head, sinuses, and face. The resultant images were retrieved from the institution's
digital archive system (when available) and analyzed using the Osirix software program
(Pixmeo, Switzerland) to calculate the area of the skull base defect.
Surgical technique
All cases were performed under general anesthetic, without the use of lumbar drain
during the intra or postoperative periods, and prophylactic antibiotics were given
in accordance with prevailing guidelines of the local hospital infection advisory
committee.
After general anesthesia, patients were placed in the dorsal decubitus position with
head clamped in a 3-pin fixation device. The head segment was positioned, relative
to the body, with slight flexion, rotated to the right, and inclined to the left.
The nasal cavity was prepared using asepsis followed by the application of a topical
vasoconstrictor (adrenalin diluted in distilled water 1:1000). High-definition video
and camera (Stryker 1488, Kalamazoo, MI, USA) were employed for the operation together
with a 0, 30° and 45° Karl-Storz Hopkins II endoscope (Tuttlingen, Germany). All extended
endoscopic endonasal approaches in the institution are performed jointly by the neurosurgery
and otorhinolaryngology teams using the “4 hands” technique.
The procedure commenced with middle turbinectomy to the right with preservation of
the upper third, followed by ipsilateral anterior and posterior ethmoidectomy. Except
in cases with specific surgical indications or anatomical abnormalities, routine nasoseptal
flap in the right nasal fossa was performed.[[7]],[[8]],[[11]],[[14]]
The nasoseptal flap is produced by making a superior incision just below the sphenoid
ostium, continuing anteriorly toward the nasal septum, preserving approximately 1.5
cm of the superior portion of the septal mucosa to prevent olfactory injury, and extending
to the columella region. The inferior incision is made just above the choana arch,
creating a pedicle around 1.5 cm wide, where this must be preserved because it contains
branches of the sphenopalatine artery which irrigates the septal mucosa. To achieve
a large pedicled flap, in all cases, the incision was extended anteriorly along the
nasal fossa floor below the inferior concha.
After producing the nasoseptal flap, the vomer and perpendicular plate of the ethmoid
were removed, preserving 1.5 cm superiorly at the bone-cartilage transition point
(posterior chondrotomy), creating a single posterior cavity to access both nostrils
concomitantly. After chondrotomy, the posterior portion of the mucosa contralateral
to the nasoseptal flap was used to patch the exposed cartilage of the nasal septum
after producing the nasoseptal flap, as described by Caicedo-Granados et al. and denoted
the reverse flap,[[15]] followed by placement of the nasal splint.
A large sphenoidectomy was performed to allow good visualization of the target area
and facilitate handling of the surgical instruments, entailing complete exposure of
the tuberculum sellae and planum sphenoidale [[Figure 2]] and [[Figure 3]]a. After creating the nasoseptal flap and due preparation and exposure of the nasosinus
cavity, the planum sphenoidale, tuberculum sellae and sella can be carefully drilled
to the depth required for tumor resection [[Figure 3]]b and [[Figure 3]]c.
Figure 2: Imaging in cadaver using 0o optic. (a) Exposure of whole posterior wall of sphenoid
sinus, for performing craniectomy using endoscopic approach. (b) Green highlights
showing whole region of bone opening for access to tuberculum and planum sphenoidale
region, exposing dura-mater. (c) Opening of dura-mater in region of upper boundary.
(d) Opening of dura mater allows visualization of hypophyseal stalk, superior hypophyseal
artery, optic chiasm and superior intercavernous sinus
Figure 3: Intraoperative view. Step by step of endoscopic surgical field using 0°, 30° and
45° optics respectively. (a) Panoramic view of the posterior wall of the sphenoidal
sinus. A large sphenoidectomy was performed to allow good visualization of the target
area. (b) Dura mater after the opening of the sellar floor and suprasellar region
(craniectomy). (c) Enlargement of the initial craniectomy using a Kerrison Roungeur
This stage constitutes the endoscopic craniectomy in an inverted trapezoid shape;
the lower boundary is the upper region of the sella (superior intercavernous sinus);
the lateral boundaries are the optic canals, and the upper border depends on the anterior
extension of the tumor, where very anterior planum sphenoidale tumors can reach as
far as the region of the cribriform plate [[Figure 2]].[[12]]
To improve control of bleeding during the operation, dural veins should be coagulated
beforehand, as well as the ipsilateral McConnell capsular artery (or both in larger
tumors), which is often hypertrophied and predominantly responsible for irrigating
the tumor.[[16]],[[17]]
The dural opening is made close to the midline, and the lesion thus identified. For
larger tumors, tumor debulking is first carried out by removing intratumor fragments
to aid manipulation. Subsequently, extracapsular dissection is commenced, observing
the arachnoid planes surrounding the tumor to prevent damage to adjacent vascular
or nerve structures [[Figure 4]]a.[[6]],[[18]]
Figure 4: (a) The dural opening is made close to the midline and the lesion is thus identified,
tumor debulking is first carried out by removing intratumor fragments to aid manipulation.
(b) Removing the entire tumor after be dissected from adjacent structures. (c) After
tumor resection, copious irrigation of the surgical cavity is mandatory, along with
thorough hemostasis
Traction and movement of the tumor must be done delicately in a bid to identify adherence.
Only when all adherences have been detached by direct visualization can the tumor
be removed. The tumor must not be removed aggressively, tractioning it downward, without
first using the standard microsurgical traction and contra-traction techniques, while
protecting key structures. The tumor can then be dissected from adjacent structures
[[Figure 4]]b. After resection, copious irrigation of the surgical cavity is mandatory, along
with thorough hemostasis [[Figure 4]]c.[[6]],[[18]]
The next stage is to harvest the fascia lata, where the lower limb has been placed
in the position since the outset of surgery and aseptic preparation of the skin previously
carried out. In general, slight bending of the knee and inner rotation of the hip
aids the removal process.
A straight 3–4 cm incision is made into the anterolateral surface of the thigh with
its axis parallel to the crural fascia. When necessary, the incision can be extended
to 10–12 cm according to the size of the graft needed. In the present study, grafts
measuring approximately 5 cm 2 sufficed.[[19]],[[20]]
After the thigh incision, fat can be collected if necessary. The dissection is deepened
until identifying the fascia lata. The size of the graft to be removed can be slightly
larger than the dural defect and after removal is preserved in saline until use. Hemostasis
is checked to ensure no coagulations or hematomas within the incision and closure
is layered using 2.0 nylon suture to draw together the removed fascia, followed by
monocryl 3.0. Nylon suture 3.0 or 4.0 is used for skin closure and stitches are removed
10–15 days later depending on wound healing.
After tumor removal, irrigation and hemostasis are performed and the graft is inlayed
into the skull base defect [[Figure 5]]a. This step must be done without folding, and the endonasal craniectomy region
must be covered fully [[Figure 5]]b. The onlay nasoseptal flap must then be placed, with the perichondrial surface
position onto the osseous part of the skull base [[Figure 5]]c. When positioning the flap, the surgeon must ensure the pedicle does not become
twisted as this will compromise the irrigation of the flap and lead to necrosis [[Figure 5]]d.[[21]],[[22]]
Figure 5: (a) After harvested the fascia lata graft is placemented within of craniectomy. (b)
Dural reconstruction was performed with an inlay fascia lata graft. (c) The onlay
nasoseptal flap must then be placed with the perichondrial surface position onto the
osseous part of the skull base and the pedicle does not become twisted as this will
compromise irrigation of the flap and lead to necrosis. (d) The craniectomy region
must be covered fully
To prevent displacement during patient movement, a number 16–18 Foley catheter is
placed and inflated with direct visualization to guarantee mechanical support for
the skull base reconstruction. Both nostrils are plugged with gauze pads soaked in
antibiotic cream.
During the first 24 h after the surgery, patients must be rested. Walking is commenced
24 h after the surgical procedure. Patients must refrain from physical exertion and
other activities which may increase intracranial pressure, for 4 weeks after the procedure.
The nasal plug is removed on the 3rd–5th postoperative day.
Results
A total of 10 patients (1 male: 9 female) satisfying the inclusion and exclusion criteria
were selected, of whom 8 had tuberculum sellae meningiomas. Preoperative tumor size
was also measured for 6 patients revealing an average volume of 13.42 cm 2. Analysis
of the postoperative skull base dural defect was carried out, having a mean area of
3.5 cm 2. No intraoperative complications were reported. Results of the analysis of
demographics and tumor for each case are given in [[Table 1]] and [[Figure 6]].
Table 1: Results obtained in the case series
Figure 6: Computed tomography image of head performed in first 24 hours postoperatively using
Osirix software (Pixmeo, Switzerland) showing area and size of craniectomy. Image
reconstruction on sagital, coronal and axial planes. (a) Image showing tuberculum
sellae; and (b) planum sphenoidale meningioma craniectomy
At the 1-year postoperative follow-up, no patients had developed meningitis or CSF
leak.
One patient had an infectious complication indirectly related to the surgical procedure
(fungal ball in right frontal sinus) 6 months after surgical meningioma resection.
The condition evolved with moderate-to-severe headache in the right frontal sinus
region and was diagnosed using CT face sinus scan. Combined Draf IIb surgery via an
external approach (lynch incision) was performed with complete resolution of the clinical
picture.
Another patient, on the 15th postoperative day, developed amaurosis and paresis of
the abducens nerve (CN VI), whose investigation using head MRI disclosed a brain abscess
which required external surgical intervention and endovenous antibiotic therapy for
6 weeks. The patient made a full recovery after the treatment. The information on
patients included in this series is summarized in [[Table 1]].
Discussion
A host of complications have been reported after endoscopic skull base surgery, such
as hyposmia, nasal synechiae, nasal obstruction, transient or permanent hormone changes,
and face paresthesia. However, CSF leakage and meningitis are relatively common complications
that have a major impact on patient satisfaction and postoperative outcome.[[14]],[[23]],[[24]]
These complications are more common in EEA because of high-flow CSF leakage, given
that breaching of the arachnoid plane, opening of the high-flow CSF cisterns or the
ventricular system and large dural skull base defect occur with this approach, where
these events were seen for all the cases in the present study. High rates of CSF leakage
have been previously described (40%–50%) in EEAs. However, following the description
and dissemination of multi-layer reconstruction in association with the nasoseptal
flap, this rate has declined dramatically <3%.[[7]],[[10]],[[23]],[[24]],[[25]]
Harvey et al.[[26]] performed a systematic review analyzing endoscopic skull base surgery procedures
with large dural defects (>3 cm 2) and intraoperative CFS leakage, and concluded that
the use of vascularized flaps in the reconstruction of these large defects resulted
in a postoperative CSF leak rate of 6.7%. This difference was statistically significant
compared with a series using free grafts only. Other advantages of vascularized flaps
are early epithelization, allowing earlier introduction of complementary therapy (radiotherapy)
with lower rates of late leaks secondary to these treatments.[[7]],[[10]],[[13]],[[14]],[[24]],[[27]]
Some nuances regarding nasoseptal flaps are noteworthy, including the fact that the
mucosa around the dural defect should be fully removed to allow the flap to make direct
contact with the bone, else there is poor adherence of the vascularized flap, increasing
the rate of CSF leakage. Nonremoval of the mucosa can also increase the risk of mucocele
formation under the flap.[[28]],[[29]],[[30]]
Another important nuance for the closure of large skull base defects is that, when
producing the nasoseptal flap, to make the more lateral inferior and superior incision
and lower close to the sphenopalatine foramen, thereby allowing greater rotation and
anteriorization of the resultant flap.[[7]],[[8]],[[9]]
In cases where the sphenoid sinus presents postsella pneumatization, fat from the
abdomen or lower limb can be used to support the pedicle and its more posterior portion,
thereby increasing its anterior reach.[[27]] In the present casuistic, use of fat in the reconstruction was not necessary. Finally,
the flap should be fully supported against the skull base, with no dead space between
the flap and skull base, as this also increases the risk of postoperative CSF leak
[[Figure 7]].[[7]],[[8]],[[9]]
Figure 7: Magnetic resonance imaging at 6 months postoperatively showing well-lodged fascia
lata inlay and nasoseptal flap and absence of “dead space” between nasoseptal flap
and sphenoid sinuses, important for preventing post-operative cerebrospinal fluid
leakage
Large skull base defects with high-flow CSF leaks, require careful multi-layer reconstruction
using both autologous and heterologous materials.[[10]],[[12]],[[23]],[[27]],[[31]],[[32]],[[33]],[[34]] The technique employed in the present study, akin to that in Eloy et al.,[[12]] involved two-layer closure with autologous material, being an inlay fascia lata
graft and an overlay vascularized flap, without use stitches or fibrin glue. This
promoted a high level of efficacy, with no cases of CSF leakage or meningitis or complications
involving the donor site (lower right limb).
The results suggest this is an effective and low-cost repair technique, in which only
autologous material (fascia lata and nasoseptal flap) was used in the present study
for defect reconstruction, dispensing with the need for dural substitutes, a rare
situation in the literature.[[8]],[[33]],[[34]] The nonuse of heterologous materials for dural closure, its high efficacy and low
cost makes this technique replicable in many centers.
Two cases of infectious complications were observed in the present series, although
the fungal ball was not directly related to the surgery. By contrast, the second case
with brain abscess was directly associated with the surgery. The use of fascia lata
has been routine in neurosurgery since the 1990s and has proven safe with low infection
rates (2.3%).[[35]],[[36]] However, we do not attribute the infectious complications in the present series
to the materials used, given the autologous materials were harvested from the donor
site at the time of use.
The use of fat for defect closure, particularly in the skull base, is also routine.
Despite publications reporting the safety of fat use,[[37]] there have been some reports of complications related to its intradural use, such
as aseptic meningitis, lipoid dissemination by the meninges, and local inflammatory
reaction.[[38]],[[39]],[[40]],[[41]] In view of these problems, the proximity to delicate nerve structures, such as
the optic apparatus and vascular structures, together with the team's experience at
our institution, we avoid intradural fat, reserving its use for the sinonasal cavity
when the flap requires mechanical support. This use was not needed in any of the cases
reported.
The area of the endonasal craniectomy was 3.58 cm 2 in the present study, lower than
the average reported by Eloy et al. of 5.6 cm 2.[[12]] The craniotomy area directly correlates with tumor location and size and tends
to be greater in planum sphenoidale meningiomas. With the accrual of more years of
experience, our team is now using increasingly larger dural openings, owing to the
higher surgical safety for tumor removal and dural defect repair.