Abstract
A variety of sinonasal tumours, meningiomas or other lesions of the anterior skull base involve the paranasal sinuses and the periorbital area. The transbasal approach (TBA) has turned out to be a feasible technique to reach those lesions. A retrospective review at a neurosurgical university department between November 2007 and January 2020 with adult patients who underwent resection of oncologic pathologies through TBA. Surgical technique, extent of resection (EOR), clinical outcome and postoperative complications were analysed. 18 TBAs between November 2007 and January 2020 were performed. Median age was 62 (range 25–83), 7 female and 11 male patients. Gross total resection rate was 85.8% throughout all entities. Four (22.2%) patients suffered from WHO°I meningiomas and 14 (77.7%) from other extra-axial lesions. Preoperative Karnofsky Performance Status Scale (KPSS) was 80% (range 40–90), postoperative KPSS 80% (range 20–100). Rate of postoperative complications requiring intervention was 16.7%. Median follow-up was 9.8 (range 1.2–71.8) months. Modifications and extensions of the classic TBA are not mandatory. Complete resection can be performed under functional and cosmetic-preserving aspects. Second-step procedures such as transnasal approaches may be performed to avoid high morbidity of more aggressive TBAs, if necessary. Surgical considerations should be kept simple and straightforward.
Subject terms: Outcomes research, Brain, Head and neck cancer, Surgical oncology
Introduction
Oncologic lesions in the anterior skull base with transbasal infiltration and involvement of the paranasal sinuses and orbit have always been surgically challenging due to the anatomic relationships in this region. These skull base tumours can originate from a variety of structures such as paranasal sinuses, nasal pharynx, leptomeninges and orbital or cranial nerves, as well as from the squamous cells or the glands1,2.
The transbasal approach (TBA) turned out to be an advanced but feasible approach to expose deep-lying lesions of the anterior skull base.
Since its first usage and systematic description by Frazier, Tessier, Derome and Dandy3–6, several variations, extensions and alternatives have been described and discussed in the last decades by technical notes, cadaver studies and small sample series1,7–12. Modifications have been made to the original technique such as removal of the supraorbital bar, ethmoidectomy, sphenoidectomy and extradural resection of the clivus.
Beals and Joganic tried to incorporate TBAs but could not applicate sufficiently to the current literature13. Therefore, Feiz-Erfan et al. categorized and proposed a classification for the TBA to facilitate the comparison and discussion of these approaches5.
However, due to greater technical variety, rarity and technically demanding nature of the TBA, only few larger series such as Liu’s, Lang’s, Raso’s or Barzaghi’s series with 15, 18, 20 and 21 patients, respectively, exist regarding surgical considerations, perioperative morbidity/mortality, follow-up and outcome1,14–18.
This study aims to highlight the sufficiency of simple TBAs without further modifications and osteotomies and thus the reduction of perioperative morbidity. Researchers have accepted little pathological heterogeneity to discuss this problem from a surgical and technical point of view.
Materials and methods
Study population and clinical parameters
We performed a retrospective review of our clinical database. From November 2007 until January 2020, we screened the clinical documentation files and neuropathological records of adult patients (≥ 18 years old) who underwent surgery through a TBA for extra-axial oncologic lesions. Eighteen patients could be identified who were operated with this technique.
We analysed clinical patient files for neurological symptoms, Karnofsky Performance Status Scale (KPSS), postoperative new permanent neurological deficits, postoperative complications and re-interventions. We defined the total rate of postoperative new deficits/complications/reinterventions as the number of events divided by the number of patients. Then, we recorded the type of TBA (according to Feiz-Erfan et al.)5 and histopathological entity. Radiological outcome parameters consisted of anatomic location as well as the extent of resection (EOR) according to postoperative cranial magnetic resonance imaging (MRI).
Statistical evaluation
We performed descriptive statistical analysis using STATA Version 13.1 (2011, StataCorp, College Station, Texas).
In descriptive data analysis, non-normally distributed data are shown as median and interquartile range (IR), and normally distributed variables are shown as mean and standard deviation.
Surgical technique
Previous publications5,6,11,19 have described in detail the operative techniques and nuances for the classic TBA. In fact, we did not use any noteworthy alterations of known techniques, but we advocate regular usage of a navigation system, if applicable, for individually optimized craniotomy. As already mentioned, we just performed level 0 TBAs according to Feiz-Erfan et al.5.
The patient is placed in the supine position with the head slightly extended or flexed based on the vertical tumor extent. The head position mobilizes the frontal lobes away using gravity. The head typically does not require rotation for the transbasal lesions. A bicoronal incision is performed. This incision should be as anterior as possible while staying behind the hairline. The incision may not always has to to reach the tragus, but at least the level of the superior edge of the pinna. The extent of the head flexion is tailored based on the cranial extension and inferior reach of the lesion into the nasal sinuses. The scalp incision should leave the pericranium, temporalis muscle, and fascia intact. We elevate a vascularized galea-periosteum graft as a separate layer. This vascularized graft will be reflected and based anteriorly along the orbital rims. The flap is elevated, stretched, and kept moist during the operation by covering it with a wet piece of sponge. A bifrontal craniotomy along the orbital roofs follows. Burr holes in the forehead should be avoided for cosmetic reasons. The vertical height of the craniotomy is under 10 cm in most cases, however, we prefer large bone flaps for satisfying exposure and, if necessary, better cerebrospinal fluid release and further frontal lobe relaxation. Extradural dissection and lobar elevation away from the Crista Galli and exposure of the cribiform plate are performed. The dura is mobilized from the orbital roof and Crista Galli. Sharp delicate dissection is used over the olfactory bulb to disconnect the bulb and expose possible anterior extradural extension of the transbasal lesion.
Upon elevation of the bone flap, the frontal sinus mucosae are thoroughly removed and filled with antiseptic sponges Transbasal lesions need full exposure. In such cases, besides cranialization of the sinus, meticulous dural reconstruction and skull base coverage must be performed, whereas we prioritize usage of a galea-periosteum flap. We moved away from using fascia lata in the first place as we experienced more CSF leaks than with the flap, which may be based on insufficient vascularization. Necrosis and thus also source of superinfections may be further consequences. However, this just reflects our own institutional experience, whereas techniques of anterior skull base reconstruction have been extensive discussed and algorithms proposed20–22.
Ethics approval
The local ethics committee of the Technical University Munich, School of Medicine (231/20 S-EB) (Ethikkommission der Fakultät für Medizin der Technischen Universität München), approved our study. We conducted it in accordance with the ethical standards of the 1964 Declaration of Helsinki and its later amendments23.
The requirement for written informed consent was waived by the ethics committee (Ethikkommission der Fakultät für Medizin der Technischen Universität München).
Results
Patient population
Eighteen patients underwent surgical resection through a TBA between November 2007 and January 2020. Median patient age at time of surgery was 62 (range: 25–83) years. Seven (38.9%) female and eleven (61.1%) male patients were included: five (27.8%) were asymptomatic, and tumours were discovered incidentally during routine check-ups, diagnostic workup for sinusitis or, as in exemplary case 1, after a fall at home (Fig. 1); and 13 (72.2%) patients were symptomatic, which included cephalgia, headache, cranial nerve deficits (amaurosis/anosmia) and other symptoms. Median preoperative KPS was 80% (40–90), and median postoperative KPS was 80% (range 20–100). Table 1 provides further detailed demographic and clinical information. Preoperative anosmia was prevalent in 44.4% (8) of the patients, and preoperative visual deficits was prevalent in 22.2% (4).
Figure 1.
Exemplary case 1: a 74-year-old female patient admitted after fall at home and back pain. Cranial routine CT scan displayed a huge transbasal bone infiltrating and destroying a tumor with sinonasal affection. (A,B) Preoperative T1-weighted gadolinium-enhanced MR imaging showing sinonasal and orbit-infiltrating tumor with subtotal anterior skull base destruction. (C,D) Postoperative MR control showing successful resection. Reconstruction was performed with split-bone graft and galea-periosteum flap. Pathologic findings revealed adenoid cystic carcinoma. The patient recovered well from the procedure; she underwent VP-shunt implantation in further course.
Table 1.
Demographics, preoperative and tumor characteristics.
| Demographics, % (N) or mean/median (SD/range) | Total (18) |
|---|---|
| Age | 62 (25–83) |
| Sex | M 61.1% (11) |
| F 38.9 (7) | |
| Clinical presentation % (N) | |
| Preoperative KPS | 80 (40–90) |
| Asymptomatic | 27.8% (5) |
| Visual deficits/ Anopsia | 5.6% (1) |
| Amaurosis | 22.2% (4) |
| Headache | 44.4% (8) |
| Concentration/ memory/ cognition impairment | 5.6% (1) |
| Psychomotoric disorders/ dizziness/ vigilance | 5.6% (1) |
| Breathing problems | 16.6% (3) |
| Vertigo | 5.6% (1) |
| Exophthalmos | 11.2% (2) |
| Diplopia | 5.6% (1) |
| Epistaxis | 5.6% (1) |
| Rhinorrhoea/epiphora | 5.6% (1) |
| Tumor entity % (N) | |
| Meningioma | 22.2% (4) |
| Metastasis | 5.6% (1) |
| Adenoid cystic carcinoma | 16.7% (3) |
| Invasive squamous cell carcinoma | 5.6% (1) |
| Papillary transitional carcinoma | 5.6% (1) |
| Sinonasal intestinal adenocarcinoma | 16.7% (3) |
| Esthesioneuroblastoma | 27.8% (5) |
Tumor entities, location and approach-related findings
Histopathological analysis revealed four (22.2%) cases with WHO°I meningiomas, one (5,6%) metastasis, three (16.7%) adenoid cystic carcinomas, one (5.6%) invasive squamous cell carcinoma, one (5.6%) papillary transitional carcinoma, three (16.7%) sinonasal intestinal-type adenocarcinoma and five (27.8%) esthesioneuroblastomas). All TBAs were level 0 TBAs according to Feiz-Erfan et al.5 (Figs. 1, 2, 3, 4, 5). The most common tumor infiltration and destruction occurred into the orbit/orbital fissure/optic canal in 13 (72.2%) cases, followed by infiltration into the planum sphenoidale in ten (55.6%) and into the frontal sinus in nine (50.0%) cases (Table 2). The most commonly used technique for skull base reconstruction was creating a split bone graft and dural plastic via galea-periosteum-flap in 16 (88.9%) cases, respectively. Facia lata, Fibrin glue and collagen-based graft were used in two 11.1%, respectively (Fig. 4). Titan mesh was only used once.
Figure 2.
Exemplary case 2: a 70-year-old male patient presented with recurrent left eye inflammations and swelling over medial canthus. Ophthalmic examination revealed obstructed nasolacrimal ductus. (A,B) Preoperative T1-weighted gadolinium-enhanced MR imaging showing sinonasal and left orbit-infiltrating tumor. Ethmoidal and sphenoid sinus are completely infiltrating. Left bulbus is suppressed. (C,D) Postoperative MR control showing successful resection. Orbit, sphenoid and tuberculum sellae reconstructions were performed with split-bone graft, galea-periosteum flap and fibrin glue. Pathologic findings revealed metastasis of malign melanoma. The patient underwent endoscopic transnasal, sublabial reresection in the subsequent course.
Figure 3.
Exemplary case 3: a 60-year-old female patient with left amaurosis and right progressive visual deficit after two-timed resection of transbasal meningotheliomatous meningioma WHO grade I through a bifrontal craniotomy. (A,B) Preoperative T1-weighted gadolinium-enhanced MR imaging showing frontobasal meningioma with olfactory grove, ethmoidal and sphenoidal sinus and intrasellar affection. (C,D) Postoperative MR control showing Simpson II resection. Extradural clinoidectomy was performed in this case as well. Reconstruction was performed with split-bone graft and galea-periosteum flap. The patient recovered well from the procedure and underwent radiotherapy after multidisciplinary tumor board discussion.
Figure 4.
Exemplary case 4: a 78-year-old male patient with bilateral amaurosis, anosmia and psychomotoric disorders. Known sinusinal intestinal adenocarcinoma after endonasal biopsy. Radiotherapy was already carried out. Transnasal microscopic tumor debulking was performed a priori. (A–C) Preoperative T1-weighted gadolinium-enhanced MR imaging showing the huge infiltrating transbasal tumor with right orbital destruction and maxillary sinus affection. Reconstruction was performed with split-bone graft, galea-periosteum flap and collagen-based dura graft. No postoperative CSF leak occurred. (D–F) Postoperative MR control showing subtotal resection. F Small tumor remnant in the right periorbital.
Figure 5.
Exemplary case 5: a 64-year-old male patient with anosmia, rhinorrhoea, epiphora and headache. Transnasal biopsy revealed sinusinal intestinal adenocarcinoma. (A,B) Preoperative T1-weighted gadolinium-enhanced MR imaging endonasal tumor with transbasal infiltration into sphenoid sinus, cribriform plate and dislocation of right periorbit. (C,D) Postoperative MR control showing subtotal resection with questionable tumor remnant at inferior medial orbital wall. Tumor-infiltrated medial orbital walls and orbit roofs were resected. Reconstruction was performed with split-bone graft and galea-periosteum flap. Titan mesh was used as well. A second-step endoscopic procedure was performed for oncological gross total resection.
Table 2.
Skull base tumor infiltration and performed reconstruction techniques.
| Skull base involvement/infiltration % (N) | Total (18) |
|---|---|
| Ethmoidal cell | 44.4% (8) |
| Planum sphenoidale | 55.6% (10) |
| Orbit/orbital fissure/optic canal | 72.2% (13) |
| Crista galli | 1.3% (6) |
| Endonasal | 33.3% (1) |
| Frontal sinus | 50.0% (9) |
| Sphenoidal sinus | 27.8% (5) |
| Maxillary sinus | 22.2% (4) |
| Pterygoid fossa | 11.1% (2) |
| Dural/bone reconstruction technique | |
| Split graft | 88.9% (16) |
| Galea-periosteum flap | 88.9% (16) |
| Fascia lata | 11.1% (2) |
| Fibrin glue | 11.1% (2) |
| Titan mesh | 5.6% (1) |
| Collagen-based graft | 11.1% (2) |
Extent of resection, outcome and surgical complications
Gross total resection was achieved in 85.8% throughout all entities. Regarding meningiomas, Simpson grade I and II resection rate was 100.0% (Fig. 3). In order to achieve oncological total resection, a neck-dissection and a second-step transnasal endoscopic procedure (Fig. 2) were performed in three other cases. In one case an orbital exenteration was performed additionally.
Postoperative total complication rate was 33.3%. Venous congestion (11.1%) and one complication of pneumocephalus were classified as minor complications, as there was no necessity of urgent intervention. One complication of wound healing disorder and one of shunt-dependent hydrocephalus (5.6%, respectively) occurred in further follow-up. Therefore, rate of postoperative subsequent moderate-to-severe complications was 16.7% (Cerebrospinal fluid (CSF) leak 11.1%, chronic subdural hematoma (SDH) 5.6%).
Complication dependent re-intervention rate was 38.9% (Table 3). A revision due to CSF leak was necessary in 11.1% and due to haemorrhage in 5.6%. In one case, we performed a pedicled latissimus dorsi flap plasty24 (5.6%) due to wound healing disorders with abscess and consecutive bone ex- and implantation (5.6%).
Table 3.
Extent of resection and postoperative outcome.
| Postoperative presentation % (N) or mean/median (SD/range) |
Total (18) |
|---|---|
| Complete resection rate (Simpson grade I + II and GTR) | 85.8% |
| Extent of resection in case of other than meningioma |
GTR 57.1% (8/14) STR 33.3% (6/14) |
| Simpson grade I–IV in case of meningioma |
I 75%% (3/4) II 25% (1/4) |
| Intraoperative complications | Vascular (ACA injury) 5.6% (1) |
| Postoperative complications |
Minor complications Pneumocephalus 5.6% (1) Venous congestion 11.1% (2) Major complications CSF leak 11.1% (2) SDH 5.6% (1) During follow up: WHD 5.6% (1) Hydrocephalus 5.6% (1) |
|
Postoperative interventions In further course |
Revision due to CSF leak 11.1% (2) Revision due to haemorrhage 5.6% (1) During follow up VP-shunt 5.6% (1) Bone explant/implant 5.6% (1) Pedicled latissimus dorsi flap plasty 11.1% (2) |
| New permanent neurological deficits |
Psychomotoric disorders 11.1% (2) Dysphagia 5.6% (1) |
| Postoperative KPS | 80.0% (20–100) |
| Follow-up time in months | 9.8 (1.2–71.8) |
Median follow-up was 9.8 (1.2–71.8) months (Fig. 6).
Figure 6.
Illustration of classic basal bifrontal craniotomy for transbasal approach, complete resection rates, postoperative outcome and complications.
Discussion
In our patients, TBA is a technically demanding but satisfying operative technique to expose a deep, transbasal-lying lesion in the anterior skull base, the midline structures and the interhemispheric fissure. In the majority of cases, complete resection without a new neurological deficit could be achieved. Complete resection rate (Simpson grade I + II and GTR) was 85.8% with a total complication rate of 33.3%. Rate of postoperative complications requiring intervention was 16.7%. No surgery-related death occurred. According to the proposed classification by Feiz-Erfan et al., all performed TBAs were level 0 basic TBAs (Fig. 7).
Figure 7.
Illustrative case of classic transbasal approach. (A) Typical skin incision and preparation of a galea-periosteum flap for later reconstruction. (B) Bifrontal craniotomy. (C,D) Macroscopic view after bone flap elevation. (E) After initial tumor debulking further exploration by resection of lateral sphenoid wing. (F) Periorbit and left maxillary sinus exposed. (G) Removal of optic strut. (H) Exposure of opticocarotid triangle. (I) Subfrontal, transethmoidal, transsphenoidal and transmaxillary exposure. (J) Macroscopic overview after complete tumor resection. (K) Anterior skull base reconstruction is performed by galea-periosteum flap. (L) Bone flap re-implantation using thin flaps and closure.
The TBA is a widely used anterior, midline and craniofacial approach with a variety of modifications and extensions. Derome initially popularized TBA for midline pathologies of the anterior skull base6. One of the big advantages is the ability to avoid a transfacial procedure and to allow craniofacial resection by a craniotomy-only technique11.
Many attempts for a classification have been made13, for example, to divide the approach into 3 subgroups: “traditional,” “extended” and “extensive”11. Traditional TBA has been defined as a simple bifrontal craniotomy. The “extended” TBA includes the removal of medial supraorbital rims between the supraorbital notches, whereas the “extensive” TBA includes complete removal of the supra-orbital bar. However, surgical techniques have developed further, and other extensions or modifications of already existing variations have been added to the conglomeration of TBAs. Feiz-Erfan et al. summarized these modifications and provided a new classification system to unify the TBA terminology of the past decades5. They proposed four levels, ascending in extension: level 0 TBAs, as consistently performed by us, consists of a classic bifrontal craniotomy without facial osteotomies. The other classes encompass more aggressive osteotomies up to canthal ligament resection with canthopexy, such as in level 3 TBAs.
Anyway, many authors have described their techniques and style of approach, where complication rates have ranged from 30 to 50%, but they have also described rates over 70%5,11,18,25–32. Our complication rate of 33.3% is in the lower bound of those findings. One should notice that we resected all lesions by level 0 TBAs (Figs. 1, 2, 3, 4, 5). Other authors have described complete resection rates between 80 and 93%16,25,29, which are congruent to our rate of 85.8% using a relatively simple technique. We did not see any urgent need for extensive osteotomies. On the contrary, we preferred second-step transnasal endoscopic re-resections in further clinical courses to achieve oncological R0-resection in 16.7% (3) in order to avoid cosmetic deformity and higher perioperative morbidity. With targeting the lesions with another angle of view by more minimal-invasive approached such as above-mentioned endonasal techniques in a second step, the TBA may be kept as simple as possible. In general, implementation of minimally invasive approaches wants to benefit from endoscopy33–35, such as the endoscopic endonasal approach. However, literature shows that only certain cases are suitable and extent of resection is only 66.7% for an endonasal endoscopic approach in case of midline meningiomas of the anterior skull base34,36. Open transcranial approaches for olfactory groove meningiomas, for example, still result in higher rates of total resection with lower postoperative CSF leak rates33. Purely endoscopic or endoscopy assisted resections via transnasal or transcranial routes have been popularized for some time offering minimal invasive visualization of the skull base region34,37. This trend has not peaked into a paradigm shift as extent of resection and CSF leakage rates have been described to be unfavorable compared to classic skull base approaches33–35,37, which is why a TBA should be performed primarily as done in our series.
Regarding complications, CSF leaks are considered the most common ones through TBAs, especially after dural reconstruction10,38. Postoperative leaks may be controlled with lumbar drainage as we did regularly. Otherwise, revision is necessary. In our series, a revision due to CSF leak occurred twice (11.1%), which is comparable to the findings of, for example, Obeid et al. with 20% or Raveh et al. and Kurtsoy et al. with 4.8% and 6.0%, respectively29,32,39. Regarding infections, incidence is actually low10,16,18,21,32,38. They may occur in the case of larger tumours and longer operative times requiring surgical revision with bone flap explantation and plastic flap reconstruction, as with one of our patients.
Regarding postoperative anosmia, the sacrifice of olfactory nerves is often necessary during a TBA. Researchers have attempted to minimize this loss of function. Spetzler et al. described a cribriform plate osteotomy to preserve olfaction28,40,41. In selected cases, preservation of more than 90% was reported, which other authors confirmed as well5. However, this may be practicable if transbasal infiltration just occurred to a certain extent. In the case of huge infiltrating tumours, such as nasosinal adenocarcinomas, esthesioneuroblastomas or cribriform and endonasal-infiltrating olfactory groove meningiomas, preservation of olfaction remains hardly possible. Some groups reported experimental methods. Matano et al. described a “fibrin-gelatine fixation” method to preserve olfactory function by dissection of the olfactory bulbs from the frontal lobe and by fixing them to the frontal base surrounding bulbs using a thin slice of gelatine sponge with fibrin glue. Anosmia occurred in 4 patients (8.8%), which was transient in two (4.4%) and permanent in the remaining two (4.4%) of a series of 45 olfactory groove meningiomas42.
More aggressive approaches to anterior cranial base lesions are on the rise and advocated by some. Although transfacial and transmaxillary approaches may provide reasonable surgical access, they may also be associated with a higher incidence of cosmetic deformity, CSF leak, infection and mortality10,19,43–45.
However, despite the above-mentioned heterogenous surgical philosophies, attention should be paid to the fact that we performed relative standardized TBAs without extra osteotomies or modifications in order to keep surgical processes simple and comparable. Of course, the size of craniotomy and the exact position depended on the location and size of the lesion; nevertheless, our results showed satisfactory postoperative findings regarding EOR, perioperative comorbidity and postoperative outcome. Therefore, we recommend performing TBAs if indication is comprehensible. TBAs still remain technically demanding, but if surgical considerations are kept simple and straightforward, this approach turns out to be a cosmetic and functionally justifiable technique for different transbasal tumours.
Study limitations
As it is a retrospective case series, it is not possible to draw causalities with respect to clinical outcome. Nevertheless, we implemented detailed clinical examination, including scores on functional performance, and a standardized follow-up protocol based on a certified neurooncological board into our clinical workflow. In our study, we did not focus on the long-term outcome of different tumor entities but on the surgical approach and perioperative outcome.
Besides its retrospective nature, the analysed patient collective suffers from histological heterogeneity. The presented histological entities are quite mixed. They include benign and malignant lesions. As we decided to to determine the outcomes of the technique and focus on the TBA itself we have accepted pathological heterogeneity to discuss this problem from a more surgical and technical point of view.
Conclusions
This study shows that modifications and osteotomy extensions of the classic TBA are unneeded. Complete resection can be performed under functional and cosmetic-preserving aspects. Second-step procedures such as transnasal approaches may be taken into consideration to avoid higher perioperative morbidity of more aggressive TBAs, if necessary. Surgical considerations should be kept simple and straightforward.
Author contributions
Conceptualization: A.K.A. Methodology: A.K.A, M.B, J.S.B. Formal analysis and investigation: A.K.A, M. B. Writing—original draft preparation: A.K.A. Writing—review and editing: M.B, A.W, C.D, C.N, B.M, J.G. Supervision: C.N, B.M, J.G.
Funding
Open Access funding enabled and organized by Projekt DEAL.
Data availability
The data for this manuscript can be obtained from the author upon reasonable request.
Competing interests
J.G. and B.M. work as consultants for Brainlab (Brainlab AG, Feldkirchen). In addition, B.M. works as a consultant for Medtronic, Spineart, Icotec, Relievant and Depuy/Synthes. In these firms, B.M. acts as a member of the advisory board. Furthermore, B.M reports a financial relationship with Medtronic, Ulrich Medical, Brainlab, Spineart, Icotec, Relievant and Depuy/Synthes. He received personal fees and research grants for clinical studies from Medtronic, Ulrich Medical, Brainlab, Icotec and Relievant. All this happened independently of the submitted work. B.M. holds the royalties/patent for Spineart. All named potential conflicts of interest are unrelated to this study. There are no further competing interests regarding the other authors.
Footnotes
Publisher's note
Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.
References
- 1.Raso, J. L. & Gusmao, S. Transbasal approach to skull base tumors: evaluation and proposal of classification. Surg Neurol65 Suppl 1, S1:33–31:37; discussion 31:37–31:38, doi:10.1016/j.surneu.2005.11.037 (2006). [DOI] [PubMed]
- 2.Watanabe T, et al. Surgical approach for craniopharyngioma bifrontal basal interhemispheric approach/extended endonasal endoscopic approach. No Shinkei Geka. 2011;39:849–857. [PubMed] [Google Scholar]
- 3.Silva D. Orbital tumors. Am. J. Ophthalmol. 1968;65:318–339. doi: 10.1016/0002-9394(68)93081-X. [DOI] [PubMed] [Google Scholar]
- 4.Frazier CHI. An approach to the hypophysis through the anterior cranial fossa. Ann. Surg. 1913;57:145–150. doi: 10.1097/00000658-191302000-00001. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 5.Feiz-Erfan I, et al. Proposed classification for the transbasal approach and its modifications. Skull Base. 2008;18:29–47. doi: 10.1055/s-2007-994292. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 6.Derome P. Les tumeurs sphe-no-ethmoidales: possibilitesd exerese et de reparation chirurgicales. Neurochirurgie. 1972;18:1–164. [PubMed] [Google Scholar]
- 7.Terasaka S, Day JD, Fukushima T. Extended transbasal approach: anatomy, technique, and indications. Skull Base Surg. 1999;9:177–184. doi: 10.1055/s-2008-1058144. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 8.Wongsuriyanan S, Sriamornrattanakul K. Interhemispheric approach with early A1 exposure for clipping anterior communicating artery aneurysms: Operative techniques and outcomes. World Neurosurg. 2020 doi: 10.1016/j.wneu.2020.03.005. [DOI] [PubMed] [Google Scholar]
- 9.Effendi ST, Rao VY, Momin EN, Cruz-Navarro J, Duckworth EA. The 1-piece transbasal approach: Operative technique and anatomical study. J. Neurosurg. 2014;121:1446–1452. doi: 10.3171/2014.8.Jns132609. [DOI] [PubMed] [Google Scholar]
- 10.Chandler, J. P. & Silva, F. E. Extended transbasal approach to skull base tumors. Technical nuances and review of the literature. Oncology (Williston Park)19, 913–919; discussion 920, 923–915, 929 (2005). [PubMed]
- 11.Kawakami K, Yamanouchi Y, Kubota C, Kawamura Y, Matsumura H. An extensive transbasal approach to frontal skull-base tumors Technical note. J. Neurosurg. 1991;74:1011–1013. doi: 10.3171/jns.1991.74.6.1011. [DOI] [PubMed] [Google Scholar]
- 12.Ng AF, et al. Microsurgical anatomy review of bifrontal limited transbasal approach: Quantitative and anatomy study. World Neurosurg. 2020 doi: 10.1016/j.wneu.2020.02.114. [DOI] [PubMed] [Google Scholar]
- 13.Beals S, Joganic E. Transfacial exposure of anterior cranial fossa and clival tumors. BNI Q. 1992;8:2–28. [Google Scholar]
- 14.Barzaghi LR, Spina A, Gagliardi F, Boari N, Mortini P. Transfrontal-sinus-subcranial approach to olfactory groove meningiomas: Surgical results and clinical and functional outcome in a consecutive series of 21 patients. World Neurosurg. 2017;101:315–324. doi: 10.1016/j.wneu.2017.02.039. [DOI] [PubMed] [Google Scholar]
- 15.Lang DA, et al. The extended transbasal approach: clinical applications and complications. Acta Neurochir (Wien) 1999;141:579–585. doi: 10.1007/s007010050346. [DOI] [PubMed] [Google Scholar]
- 16.Liu JK, Silva NA, Sevak IA, Eloy JA. Transbasal versus endoscopic endonasal versus combined approaches for olfactory groove meningiomas: importance of approach selection. Neurosurg. Focus. 2018;44:E8. doi: 10.3171/2018.1.FOCUS17722. [DOI] [PubMed] [Google Scholar]
- 17.Ross DA, Marentette LJ, Moore CE, Switz KL. Craniofacial resection: decreased complication rate with a modified subcranial approach. Skull Base Surg. 1999;9:95–100. doi: 10.1055/s-2008-1058155. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 18.Sekhar LN, Nanda A, Sen CN, Snyderman CN, Janecka IP. The extended frontal approach to tumors of the anterior, middle, and posterior skull base. J. Neurosurg. 1992;76:198–206. doi: 10.3171/jns.1992.76.2.0198. [DOI] [PubMed] [Google Scholar]
- 19.Lawton MT, Beals SP, Joganic EF, Han PP, Spetzler RF. The transfacial approaches to midline skull base lesions: A classification scheme. Oper. Tech. Neurosurg. 1999;2:201–217. doi: 10.1016/S1092-440X(99)80020-6. [DOI] [Google Scholar]
- 20.Gil Z, et al. A comprehensive algorithm for anterior skull base reconstruction after oncological resections. Skull Base. 2007;17:25–37. doi: 10.1055/s-2006-959333. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 21.Georgantopoulou A, Hodgkinson PD, Gerber CJ. Cranial-base surgery: A reconstructive algorithm. Br. J. Plast. Surg. 2003;56:10–13. doi: 10.1016/s0007-1226(03)00013-4. [DOI] [PubMed] [Google Scholar]
- 22.22Gök, A., Erkutlu, I., Alptekin, M. & Kanlikama, M. Three-layer reconstruction with fascia lata and vascularized pericranium for anterior skull base defects. Acta Neurochir (Wien)146, 53–56; discussion 56–57, doi:10.1007/s00701-003-0175-2 (2004). [DOI] [PubMed]
- 23.World Medical Association Declaration of Helsinki ethical principles for medical research involving human subjects. JAMA. 2013;310:2191–2194. doi: 10.1001/jama.2013.281053. [DOI] [PubMed] [Google Scholar]
- 24.Wilkman T, Suominen S, Back L, Vuola J, Lassus P. The pedicled latissimus dorsi flap in head and neck reconstruction: An old method revisited. J. Reconstr. Microsurg. 2014;30:163–170. doi: 10.1055/s-0033-1357497. [DOI] [PubMed] [Google Scholar]
- 25.Fahlbusch R, et al. Neuro-rhinosurgical treatment of aesthesioneuroblastoma. Acta Neurochir. 1989;100:93–100. doi: 10.1007/BF01403592. [DOI] [PubMed] [Google Scholar]
- 26.Feiz-Erfan I, et al. The radical transbasal approach for resection of anterior and midline skull base lesions. J. Neurosurg. 2005;103:485–490. doi: 10.3171/jns.2005.103.3.0485. [DOI] [PubMed] [Google Scholar]
- 27.Beals SP, Joganic EF, Hamilton MG, Spetzler RF. Posterior skull base transfacial approaches. Clin. Plast. Surg. 1995;22:491–511. doi: 10.1016/S0094-1298(20)30993-7. [DOI] [PubMed] [Google Scholar]
- 28.Spetzler RF, Herman JM, Beals S, Joganic E, Milligan J. Preservation of olfaction in anterior craniofacial approaches. J. Neurosurg. 1993;79:48–52. doi: 10.3171/jns.1993.79.1.0048. [DOI] [PubMed] [Google Scholar]
- 29.29Obeid, F. & Al-Mefty, O. Recurrence of olfactory groove meningiomas. Neurosurgery53, 534–542; discussion 542–533. doi:10.1227/01.neu.0000079484.19821.4a (2003). [DOI] [PubMed]
- 30.Fujitsu K, et al. Telecanthal approach for meningiomas in the ethmoid and sphenoid sinuses. Neurosurgery. 1991;28:714–720. doi: 10.1227/00006123-199105000-00013. [DOI] [PubMed] [Google Scholar]
- 31.Shah JP, et al. Craniofacial resection for malignant tumors involving the anterior skull base. Arch. Otolaryngol. Head Neck Surg. 1997;123:1312–1317. doi: 10.1001/archotol.1997.01900120062010. [DOI] [PubMed] [Google Scholar]
- 32.Raveh J, et al. Extended anterior subcranial approach for skull base tumors: long-term results. J. Neurosurg. 1995;82:1002–1010. doi: 10.3171/jns.1995.82.6.1002. [DOI] [PubMed] [Google Scholar]
- 33.Komotar RJ, Starke RM, Raper DM, Anand VK, Schwartz TH. Endoscopic endonasal versus open transcranial resection of anterior midline skull base meningiomas. World Neurosurg. 2012;77:713–724. doi: 10.1016/j.wneu.2011.08.025. [DOI] [PubMed] [Google Scholar]
- 34.Ottenhausen M, et al. Decision-making algorithm for minimally invasive approaches to anterior skull base meningiomas. 2018;44:E7. doi: 10.3171/2018.1.Focus17734. [DOI] [PubMed] [Google Scholar]
- 35.Banu MA, et al. Endoscope-assisted endonasal versus supraorbital keyhole resection of olfactory groove meningiomas: comparison and combination of 2 minimally invasive approaches. J. Neurosurg. 2016;124:605–620. doi: 10.3171/2015.1.JNS141884. [DOI] [PubMed] [Google Scholar]
- 36.Koutourousiou M, Fernandez-Miranda JC, Wang EW, Snyderman CH, Gardner PA. Endoscopic endonasal surgery for olfactory groove meningiomas: outcomes and limitations in 50 patients. Neurosurg. Focus. 2014;37:E8. doi: 10.3171/2014.7.focus14330. [DOI] [PubMed] [Google Scholar]
- 37.Mortazavi MM, et al. Planum sphenoidale and tuberculum sellae meningiomas: Operative nuances of a modern surgical technique with outcome and proposal of a new classification system. World Neurosurg. 2016;86:270–286. doi: 10.1016/j.wneu.2015.09.043. [DOI] [PubMed] [Google Scholar]
- 38.Fliss DM, et al. Early outcome and complications of the extended subcranial approach to the anterior skull base. The Laryngoscope. 1999;109:153–160. doi: 10.1097/00005537-199901000-00029. [DOI] [PubMed] [Google Scholar]
- 39.Kurtsoy A, et al. Transbasal approaches: Surgical details, pitfalls and avoidances. Neurosurg. Rev. 2004;27:267–273. doi: 10.1007/s10143-004-0322-0. [DOI] [PubMed] [Google Scholar]
- 40.Saito K, Takahashi M, Fukuta K, Tachibana E, Yoshida J. Recovery of olfactory function after an anterior craniofacial approach. Skull Base Surg. 1999;9:201–206. doi: 10.1055/s-2008-1058147. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 41.Honeybul S, Neil-Dwyer D, Lang DA, Evans BT. Extended transbasal approach with preservation of olfaction: An anatomical study. Br. J. Oral Maxillofac. Surg. 2001;39:149–157. doi: 10.1054/bjom.2000.0601. [DOI] [PubMed] [Google Scholar]
- 42.Matano, F. et al. Olfactory preservation during anterior interhemispheric approach for anterior skull base lesions: technical note. Neurosurg. Rev.39, 63–68; discussion 69, doi:10.1007/s10143-015-0647-x (2016). [DOI] [PubMed]
- 43.Carrillo, J. F., Rivas Leon, B., Celis, M. A., Ponce-de-Leon, S. & Ochoa-Carrillo, F. J. Anterolateral and lateral skull-base approaches for treatment of neoplastic diseases. Am. J. Otolaryngol.25, 58–67. doi:10.1016/s0196-0709(03)00094-2 (2004). [DOI] [PubMed]
- 44.Pendleton C, Raza SM, Boahene KD, Quiñones-Hinojosa A. Transfacial approaches to the skull base: The early contributions of harvey cushing. Skull. Base. 2011;21:207–214. doi: 10.1055/s-0031-1275631. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 45.Kim SR, Lee JW, Han YS, Kim HK. Transfacial surgical approaches to secure wide exposure of the skull base. Arch. Craniofac. Surg. 2015;16:17–23. doi: 10.7181/acfs.2015.16.1.17. [DOI] [PMC free article] [PubMed] [Google Scholar]
Associated Data
This section collects any data citations, data availability statements, or supplementary materials included in this article.
Data Availability Statement
The data for this manuscript can be obtained from the author upon reasonable request.







