Comprehensive microsurgical anatomy of the middle cranial fossa: Part II—neurovascular anatomy

In order to master the surgical approaches to the middle cranial fossa, the surgeon needs to understand the relevant bony anatomy. However, she/he also needs to have a clear and sound understanding of the neural and vascular anatomy because, oftentimes, the osseous anatomy (except for the optic apparatus) should be removed to expose and protect the neurovascular anatomy. This is the second of a two-part article discussing the neurovascular anatomy of the middle cranial fossa. A brief discussion of the surgical approaches follows.


Introduction
The middle cranial fossa (MCF) houses several important structures such as the otic apparatus and the internal carotid artery (ICA). A proper understanding of the detailed surgical anatomy of this region is critical when using approaches involving the middle fossa. This is the second of a 2-part article that focuses on the microsurgical anatomy of the neurovascular structures and briefly discusses the surgical approaches to the middle fossa.

Arterial anatomy
Two major arteries (and their branches) deserve discussion in the context of MCF anatomy: (1) ICA and (2) middle meningeal artery (MMA).

Internal carotid artery
The petrous ICA runs under the middle fossa floor in the carotid canal. It courses anteromedially almost parallel to the petrous ridge. Upon reaching the petrous apex, it makes an upward turn under the trigeminal ganglion (separated from the nerve by the petrolingual ligament) before entering the cavernous sinus ( Figure 1). The petrolingual ligament runs between the petrous apex and the lingual process of the sphenoid bone (see Part 1). It should be distinguished from the petrosphenoid ligament as the vault of Dorello's canal ( Figure 2). The petrous ICA is encased by the sympathetic plexus and embedded in a delicate venous plexus. Up to 70% of specimens are reported to have branches coming from the petrous ICA (1). Branches of the petrous ICA include (1) the caroticotympanic artery, (2) the mandibular artery, (3) the vidian artery, and (4) periosteal arteries.

Caroticotympanic artery
Reportedly, the caroticotympanic artery emanates from the posterior wall of the ICA genu between the posterior vertical and horizontal segments (2). It enters the cavity of the middle ear to feed the cavity and anastomoses with the tympanic branch of the ascending pharyngeal artery (3). It is considered a remnant of the hyoid stapedial artery (3). In some studies, no caroticotympanic branch was found (4).
A rare (yet important) branch of the petrous ICA is the persistent embryonic stapedial artery. Originating from the dorsal aspect of the first vertical segment of the petrous carotid, this artery initially serves to give rise to branches that eventually emanate from the internal maxillary artery (IMA) (i.e., inferior alveolar, infraorbital, middle meningeal, anterior ethmoidal, frontal, supraorbital, and lacrimal arteries) before it involutes (5). If the stapedial artery persists, the MMA will arise from it with the foramen spinosum (FS) being absent (1:5,000) (6). After originating from the ICA, the artery enters the hypotympanum and makes a dorsally convex curve passing through the obturator foramen of stapes. It finally exits the middle ear cavity through entering the labyrinthine facial canal end enters the middle fossa through the facial hiatus (6,7).

Mandibular artery
The mandibular artery is a remnant of an embryonic branch arising from the horizontal segment of ICA. It gives rise to two branches directed anteriorly: (a) The artery of the pterygoid canal (also known as vidian artery), which runs in the pterygoid canal, anastomosing with the vidian branch of the internal maxillary artery either in the pterygopalatine fossa or in the vidian canal. (b) The second branch courses more caudally and anastomoses with the pterigovaginal artery near the Eustachian tube (8).

Vidian and periosteal arteries
In some descriptions, the petrous ICA is considered to lack a mandibular branch and instead directly giving off the vidian and Overview of middle fossa anatomy (right side). (A) The temporobasal dura has been elevated to expose the neurovascular anatomy of the middle fossa floor. Blue area shows the middle fossa rhomboid divided by the funnel-shaped internal auditory canal (brown area) into an anterior (premeatal) triangle (1) and a posterior (postmeatal) triangle (2). Pink region denotes the Glasscock triangle. Green double-arrow shows the arcuate eminence and the trajectory of the underlying superior semicircular canal. Dashed line shows the medial petrous ridge exposed by elevation of the temporobasal dura. periosteal branches following the caroticotympanic artery (1,4). These arteries arise near the anterior genu of the petrous ICA. The vidian artery courses anteriorly and medially to reach superior and lateral to the cartilage of the foramen lacerum to enter the posterior opening of the vidian canal along with the vidian nerve. The periosteal arteries may be more than one (average of 1.5 branches per specimen) and in 45% of specimens have a common trunk with the vidian artery. These arteries supply the periosteum of the carotid canal and some may reach the dura of the middle fossa (1).

Middle meningeal artery
The MMA could originate from the IMA, ICA, basilar artery, or ophthalmic artery. However, most frequently, the MMA arises from the superior aspect of the first (mandibular) part of the IMA after the deep auricular artery (entering the squamotympanic fissure) and the anterior tympanic artery (which enters petrotympanic fissure) (See Figure 4 in Part 1). It enters FS after passing posterior to the condylar process of the mandible. Once in the MCF, the MMA grooves the greater sphenoid wing on the floor of the MCF making an anteriorly convex curve when viewed laterally. Immediately after coursing through the FS, a small trunk originates from the MMA that rapidly divides into anterior and posterior branches ( Figure 3). The posterior branch is the petrosal artery (less than 1 mm diameter), which runs posterolaterally [while being lateral to the lesser petrosal nerve (LPN)] toward the facial hiatus or a laterally located bony canal in the MCF. According to El-Khouly et al., the petrosal artery can is present in 80% of specimens. When present, the petrosal artery can arise from the MMA either above (81%) or below (19%) the FS (9). The petrosal artery supplies the greater superficial petrosal nerve (GSPN), LPN, geniculate ganglion, and facial nerve. The anterior branch is the cavernous branch of the MMA and courses anteromedially to reach the lateral aspect of the Gasserian ganglion and eventually anastomosing with the inferolateral trunk (a branch of the cavernous ICA). It gives rise to anterior and posterior divisions as it ascends laterally to reach the temporoparietal dural convexity. The point of division is usually 15-30 mm anterolateral to the FS. The anterior division further divides into medial and lateral branches. The lateral branch reaches the pterion while the medial branch courses beneath and parallel to the lesser sphenoid wing finally anastomosing with the recurrent meningeal branch of the lacrimal artery (10). As mentioned before, the MMA rarely originates from a persistent stapedial artery. The posterior division of the MMA supplies the dura of the convexity and gives two branches: (1) petrosquamosal and (2) parieto-occipital. The petrosquamosal branch runs low along the junction of the temporal bone squama and the MCF to supply the lateral and posterior dura of the MCF near and around the transverse sinus.

Venous anatomy
The MCF is like a shallow venous basin located lateral to the cavernous sinus with robust connections to the rest of the skull base venous channels. The potential space between the meningeal and endosteal layers of the dura contains venous spaces in different areas of the MCF. This potential space is prominent in the lateral aspect of the trigeminal ganglion (i.e., the laterotrigeminal venous system), anteriorly, along the sphenoid wing (sphenoparietal sinus), and medially along the petrous pyramid [superior petrosal sinus (SPS)]. The superior ophthalmic vein (SOV) runs through the superior orbital fissure (SOF) and is briefly discussed. The SPS is the medial venous sinus of the MCF connecting the cavernous and transverse-sigmoid sinuses ( Figure 4).

Superior ophthalmic vein
The SOV is the largest orbital vein. It originates in the anteromedial orbit medial to the superior rectus muscle insertion. Coursing posterolaterally between the superior rectus muscle and the optic nerve, it reaches the SOF at its lateral half outside the common annular tendon. In the SOF, it runs between the frontal nerve medially and lacrimal nerve laterally. It drains into the anterior compartment of the cavernous sinus posteriorly.

Sphenoparietal sinus
The MMA is accompanied by a venous channel between the two layers of the dura. Specifically, the anterior division of the MMA is accompanied by a robust venous space above the level of the pterion. This venous space deviates away from the MMA near the sphenoid wing and turns medially under the lesser sphenoid wing at the temporal tip to join the cavernous sinus. The venous compartment under the lesser sphenoid wing and its superolateral continuation toward parietal convexity . Less commonly (12.5% of cases), the sinus turns posteriorly to run in the basal dural of the temporal lobe and empty to the pterygoid venous plexus through the MCF foramina in which case it is called the sphenobasal sinus (13). Alternatively, in 4% of cases, it runs even more posteriorly and joins the sigmoidtransverse junction in which case it is called the sphenopetrosal sinus (13, 14).

Laterotrigeminal venous system
This is a system of venous spaces centered along the lateral edge of the trigeminal nerve root as it enters the MCF and lateral border of the Gasserian Ganglion between the two layers of the dura of the temporal base. It continues posteriorly to connect with the SPS in 94% of cases (15). Posteriorly, it joins small venous channels along the GSPN and around the FS. It extends anteriorly under the V3 as "the subtrigeminal mandibular communicating sinus" and the emissary sinus of foramen ovale (FO) on the anterolateral surface of the mandibular nerve. In 30% of cases, it extends further along the lateral border of the V3 to reach the FO. It communicates with the pterygoid venous plexus through the emissary vein of FO (15).

Superior petrosal sinus
The SPS runs along the medial ridge of the petrous part of the temporal bone from the cavernous sinus to the junction of the transverse and sigmoid sinuses. The SPS may be "complete" (i.e., connected both anteriorly to the cavernous sinus and posteriorly to the transverse-sigmoid junction-60% prevalence), "lateral" (i.e., only connected to the transverse-sigmoid junction-37% prevalence), or "medial" (i.e., only connected to the cavernous sinus-3% prevalence) (16). Once close to the trigeminal root at the entrance of Meckel's cave, it may form a venous ring around it (∼15%), or run above (∼65%) or under it (∼20%) (17,18). The most prominent tributary of the SPS is the superior petrosal vein (aka vein of Dandy). The point of entry of the vein of Dandy to the SPS varies but is most commonly between the internal auditory canal (IAC) and the point of entry of the trigeminal nerve root to Meckel's cave (19).

Neural anatomy
The MCF is a conduit for several nerves either on its floor or through the foramina and canals. Understanding the microanatomy of these nerves and their three-dimensional relationship with each other and adjacent structures is critical when performing surgical approaches in this region.

Trigeminal nerve
Meckel's cave ostium lies inferior to the SPS on the trigeminal depression of the petrous bone a few millimeters posterior to the petrous apex. It is also located just lateral to the posterior end of the cavernous sinus at the petrous apex region. The cisternal segment of the trigeminal root enters the opening of Meckel's cave and rapidly expands to form the Gasserian (aka semilunar) ganglion inferolateral to the cavernous sinus while both structures are covered with the meningeal layer of the dura of the temporal lobe (i.e., dura propria) (see cavernous sinus and Figure 6 in Part 1). Importantly, a small superomedial portion of the Gasserian ganglion is covered laterally by the posteroinferior tail of the cavernous sinus ( Figure 6) (20). The subarachnoid space extends roughly to the mid-portion of the Gasserian ganglion through the Meckel's cave ostium. The petrous ICA makes an upward turn near the petrous apex to exit the carotid canal and courses under the trigeminal nerve before entering the cavernous sinus. The petrolingual ligament, extending between the lingual process of the sphenoid bone and the lateral cornu of the petrous apex separates the ICA from the trigeminal nerve just before entering the cavernous sinus ( Figure 3). The three divisions enter their respective foramina to exit the MCF.

Ophthalmic nerve (V1)
The V1 is the smallest division of the CN V and contains somatic sensory, parasympathetic fibers from the pterygopalatine ganglion and sympathetic fibers from the plexus around the carotid artery. From the CN V ganglion, the V1 is inclined upward as it passes forward in the lower part of the lateral wall of the cavernous sinus to reach the superior orbital fissure. As the ophthalmic nerve approaches the SOF, it branches into the lacrimal, frontal, and nasociliary nerves (21). The lacrimal and frontal branches pass through the lateral sector, and the nasociliary branch passes through the central sector of the SOF (22). At the SOF, the lacrimal nerve is the most lateral nerve, while coursing above the superior ophthalmic vein. The distance between the lacrimal nerve and the lateral end of the SOF is 4.2 ± 1.7 mm. On the other hand, the nasociliary nerve gently ascends lateral to the inferior division of the oculomotor nerve while passing through the fissure, on average 11.3 ± 2.8 mm from the lateral end of the SOF (23). The inferior border of the nasociliary nerve usually gives rise to the sensory root of the ciliary ganglion in the cavernous sinus while coursing between the abducens nerve laterally and inferior division of the oculomotor nerve medially. The frontal nerve is the largest branch of the V1 division and passes through the SOF medial to the superior ophthalmic vein and the lacrimal nerve and inferior to the trochlear nerve, on average 9.3 ± 1.7 mm medial to the lateral end of the SOF (Figure 7) (23).

Maxillary nerve (V2)
The V2 is the intermediate division of the CN V and looks like a flattened band. Unlike both V1 and V3, it has only sensory functions. Contrary to many classic textbooks, more recent views hold that V2 does not course in the lateral wall of the dural envelop of the cavernous sinus, as does V1 (24). The V2 exits the middle cranial fossa through foramen rotundum (FR) to enter the pterygopalatine fossa. The laterotrigeminal venous system, which is the venous system surrounding the trigeminal nerve root and the lateral aspect of V3, may extend to the region of the foramen rotundum and lateral aspect of the V2 ( Figure 4A). The only branch off the V2 in the MCF is the

Mandibular division (V3)
The V3 is the largest division of the trigeminal nerve containing sensory, motor, and parasympathetic fibers to the salivary glands. The V3 contains efferent fibers that innervate muscles that are attached to the mandible. It is made up of two roots: a large, sensory root, which proceeds from the lateral part of the CN V ganglion and emerges through FO and a small motor root arising around the superomedial part of the main sensory root in the pons that passes below the trigeminal ganglion and unites with the sensory root just outside FO (24). The V3 exits the MCF through FO to enter the infratemporal fossa.

Greater superficial petrosal nerve
The GSPN, also known as the greater petrosal nerve, is a branch of the nervus intermedius (nerve of Wrisberg). Nervus intermedius carries parasympathetic fibers, nerve fibers for taste, and sensory fibers of the facial nerve (CN VII) (26). The GSPN contains the parasympathetic fibers originating from the superior salivatory nucleus in the brainstem reaching the pterygopalatine ganglion. It also contains taste afferents from the soft palate (to the gustatory nucleus of the solitary tract in brainstem) and sensory afferents from the dura mater and ICA to the spinal nucleus of trigeminal nerve (27). The sensory fibers pass through the ganglion and continue to the nasal cavity and palate. It is the first branch of the CN VII that arises from the geniculate ganglion. It innervates the lacrimal glands and mucous membranes of the nasal cavities and the palate as major secretory fibers. Once it arises from the geniculate ganglion, it courses anteromedially to leave the superior surface of the temporal bone through the facial hiatus and into the MCF (28). Then, the nerve courses anteromedially on the floor of the MCF, medial to LPN and lateral to ICA. It passes beneath the V3 and toward the foramen lacerum and the pterygoid canal (see Part 1, Figures 5A, 6E) (29). The point where the GSPN crosses beneath V3 is approximately 7.5 mm posteromedial on the lateral aspect of the V3 from FO (range 3-12 mm) (30). It finally joins with the deep petrosal nerve and together forms the vidian nerve. The GSPN is embedded in a meningeal dural sheath while passing on the MCF floor. This meningeal sheath is separable from the endosteal dura of the temporal lobe and this microanatomical nuance is the basis of safely exposing the GSPN while performing a middle fossa approach. The GSPN may be (at least) partially covered by bone along its passage on the middle fossa floor. The geniculate ganglion may be dehiscent in 15%-25% of cases. Also, the proximal portion of the GSPN may have no bony coverage in up to a third of specimens (4,30). These anatomical observations have led some to advocate for a frontto-back approach to potentially reduce the risk of a facial palsy during a MCF approach (30).

Lesser petrosal nerve
Three nerves contribute fibers to the LPN: (1) the tympanic branch of the glossopharyngeal nerve (Jacobson's nerve), (2) the nervus intermedius of the facial nerve, and (3) the auricular branch of the vagus nerve (Arnold's nerve). Of note, it might have a communication with the meningeal branch of V3 (31). Jacobson's nerve contributes most fibers to the LPN and arises from the inferior (aka petrous) ganglion of the glossopharyngeal nerve. Entering the tympanic cavity through the inferior tympanic canaliculus of the temporal bone, it forms the tympanic plexus on the medial wall of the tympanic cavity (mainly on the promontory). More superiorly on the promontory, the tympanic plexus converges to a single trunk Frontiers in Surgery exiting through the tegmen tympani to emerge on the MCF floor lateral to the facial hiatus and posterior to the tensor tympani muscle. Here, it is joined by a communicating trunk emerging from the geniculate ganglion to form the LPN. The communicating trunk is formed by the union of fibers from the nervous intermedius and Arnold's nerve. The fibers of Arnold's nerve are formed mainly from the superior (aka jugular) ganglion of the vagus nerve but also contain a small contribution from the inferior ganglion of the glossopharyngeal nerve. It then enters the mastoid canaliculus and enters the temporal bone between the jugular foramen and the facial canal to join the mastoid segment of the facial nerve (32). Its fibers, however, travel in a retrograde fashion to exit the geniculate ganglion while being joined by fibers from the nervus intermedius. Fibers from Arnold's nerve convey sensory information from the back of the pinna and the external acoustic meatus. Once formed, the LPN courses anteriorly on the tensor tympani muscle while being anterior and lateral to the GSPN (see Part 1, Figure 5A). Usually, the nerve is partially uncovered along its course on the MCF floor. The LPN courses an average length of 15 mm on the floor of the middle fossa before piercing the floor and exiting the fossa to join the otic ganglion. As stated in Part 1, the LPN most commonly (70%) exits the MCF through CI. Less frequently, it may exit through the FS or sphenopetrosal suture (32).

Anatomical-surgical triangles of the MCF
The MCF is a complex anatomic region and understanding its complexities could be facilitated through simplification. Translating the 3D relationships between structures using geometric shapes is one way of approaching this complexity. These have been customarily referred to as "triangles" of the skull base though they do not necessarily represent perfect geometrical trigones. The following discussion only focuses on the MCF triangles and does not include cavernous sinus and posterior fossa triangles.

Lateral triangle
This triangle is the lateral-most triangle of the MCF. Its arms include the edge of the MCF along the temporal squama laterally, the sphenosquamosal suture anteriorly, and a line between the posterior root of the zygoma and FS posteriorly (see Part 1, Figure 4A). Drilling this bony area, which is technically the roof of the infratemporal fossa, exposes the lateral pterygoid muscle, the pterygoid venous plexus, and the pterygoid segment of IMA, which can be used as a donor for intracranial bypass procedures (33).

Anteromedial triangle
Named after Sean Mullan who described it first in 1979 and used by him to surgically access the carotid-cavernous fistulas (34), this triangle is simply formed between the V1 and V2. If the greater sphenoid wing is drilled between V1 and V2, the sphenoid sinus will be exposed (see Part 1, Figure 6C).

Anterolateral triangle
First described as "lateral triangle" by Dolenc, this triangle is formed between V2 and V3 with its anterolateral border being the line connecting FO and FR (35). Other names used to refer to this triangle include "far lateral" and "lateral-most." The vidian canal passes through the pterygoid process of the sphenoid bone beneath the anterolateral triangle. Drilling the triangle posteriorly exposes the Eustachian tube and drilling it inferomedially exposes the lateral recess of the sphenoid sinus. The infratemporal fossa lies inferior to the anterolateral triangle (see Part 1, Figure 6C).

The middle fossa rhomboid
Kawase et al. described for the first time an area of the petrous bone not harboring any critical structures that could be removed to access the proximal basilar artery aneurysms (36). This area is essentially the petrous apex and resembles a rhomboid when viewed from an MCF perspective. Its boundaries include the superior semicircular canal (i.e., arcuate eminence) posteriorly, the GSPN laterally, the petrous ridge medially and the Gasserian ganglion anteriorly (see Part 1, Figure 6E). The middle FIGURE 8 Exposure of the ventrolateral aspect of the pons using right anterior petrosectomy (also known as Kawase's approach). A complete resection of the petrous apex is undertaken including the premeatal and postmeatal triangles. The cochlea (C) and arcuate eminence (AE) are preserved and the carotid canal is unroofed to expose the petrous ICA. Note how sectioning the SPS allows exposure of the entire ventrolateral aspect of the pons between the cranial nerves V and VII-VIII. ICA, internal carotid artery; SPS, superior petrosal sinus; AICA, anterior inferior cerebellar artery; GG, geniculate ganglion. Frontiers in Surgery fossa rhomboid could further be divided into premeatal and postmeatal triangles divided by the IAC (Figure 1). The premeatal triangle is essentially the Kawase triangle that could be completely drilled to expose the region between the SPS and inferior petrosal sinus (IPS). Such bony removal would provide better access to the ventrolateral pontomesencephalic and retroclival regions.

Posterolateral triangle
First described by Glasscock in 1979, this triangle permits access to the petrous ICA through drilling of the MCF just lateral to the GSPN (see Part 1, Figure 5A) (37). Boundaries of this triangle include the lateral border of the V3 distal to the point where GSPN crosses under V3 anteriorly, GSPN medially, and a line from FS to AE laterally ( Figure 1). Drilling the triangle just lateral to the GSPN will expose the petrous ICA and the Eustachian tube just lateral to it.

Surgical approaches 1
The multiple critical structures present in the vicinity of the MCF make for a suitable corridor and/or target for various pathologies    Frontiers in Surgery at FR and FO and excised to a point back beyond the Gasserian ganglion. In 1900, Harvey Cushing (1869-1939) modified the procedure by using a more basal trajectory to minimize brain retraction-his contribution decreased the mortality rate to 5% (38). Later, in 1904, Parry described the middle fossa approach for sectioning the vestibular nerve (39).

Middle fossa and extended middle fossa approaches
In 1975, Bochenek and Kukwa modified the subtemporal approach to improve the exposure of ventrolateral pons and cerebellopontine angle down to the region of the jugular foramen. They called this approach the extended middle fossa approach (40). Their modification included the drilling of the petrous bone. By doing this, 10 mm of extra space could be gained below the level of the SPS, allowing better access to the basilar artery. The major disadvantage of this modified approach is damage to hearing function due to the damage to the bony labyrinth (i.e., drilling the semicircular canals).
Later, in 1985, the "extended middle fossa approach" was further modified by Takeshi Kawase-now eponymously called the Kawase approach. Specifically, Kawase designed this approach to treat petroclival meningiomas extending into the parasellar region (i.e., sphenopetroclival meningiomas) (41). Here, in comparison to the modification of Bochenek and Kukwa, only the petrous apex is drilled. Selective drilling of the apex is advantageous because it contains no neurovascular structures while providing excellent exposure of the ventrolateral brainstem ( Figure 8). In addition, the approach has an extra step: transverse division of the tentorium to the incisura. This extra maneuver allows communication between the intradural middle and posterior cranial fossae.
The extradural middle fossa approach is also used to treat a variety of other pathologies such as petrous apex lesions, intracanalicular vestibular schwannomas, exposure of the petrous ICA as a donor for cerebral bypass procedures, and access to the infratemporal fossa to treat pathologies or to expose the IMA as a bypass donor. More recently, the term "extended middle fossa approach" is used when drilling of the MCF floor is not restricted to the petrous apex and unroofing the IAC. Basically, the surgeon could extend the drilling to the postmeatal triangle between the arcuate eminence and IAC to improve exposure of the contents of the IAC. Additionally, a limited mastoidectomy could be added if necessary (42). A full mastoidectomy with graded increase in labyrinthectomy (i.e., posterior petrosectomy) can be combined with anterior petrosectomy to provide an excellent exposure of large petroclival lesions ( Figure 9) (43,44). Further removal of the cochlea and mobilization of the zygoma will increase the surgical exposure of and maneuverability on the ventrolateral pontomesencephalic area (45). The details of these surgical maneuvers are beyond the scope of this discussion. Figures 10-12 provide case illustrations.

Subtemporal approach
In 1961, the Canadian neurosurgeon, Charles Drake (1920-1998), introduced a new surgical approach to the medial portion of the MCF called the subtemporal approach-designed for posterior circulation aneurysms (46). It is classically described as a 5 cm × 5 cm craniotomy located below the superior temporal line and centered in the coronal plane above the root of the zygoma. It requires drilling of the temporal bone to the floor of the middle fossa. The subtemporal approach is an intradural approach and the surgeon should be aware of the temporobasal veins draining the lateral parts of the basal surface of the temporal lobe into the lateral tentorial sinuses. Also, the vein(s) of Labbé draining into the transverse-sigmoid junction should be preserved.

Endonasal approaches to the middle fossa
Influential advances in endoscopic skull base surgery have validated these approaches as reasonably less invasive alternatives to the "traditional" open lateral approaches. Using the expanded corridors of the nasal and orbital cavities, the surgeon could practically access the anteromedial regions of the MCF without the need for retraction of the temporal lobe (47). Such approaches may be used for a variety of pathologies including but not limited to trigeminal neuromas, Meckel's cave meningiomas, chordomas and chondrosarcomas, juvenile angiofibromas, and other petrous Frontiers in Surgery apex lesions such as cholesterol granulomas. The final exposure arena will include the anteromedial temporal lobe dura posterior to the pterygopalatine fossa and the greater wing of the sphenoid, Gasserian ganglion, and the maxillary and mandibular nerves. Essentially, the endonasal approach involves a transpterygoid approach and the lateral aspect of the sphenoid sinus to expose the so-called "quadrangular space" lateral to the paraclival ICA and inferior to the abducens nerve (48,49). Transorbital endoscopic skull base approaches are also gaining popularity because of the direct access to the MCF. Through exposure of the frontosphenoid suture and the greater sphenoid wing, dura of the temporal pole, and anterior MCF could be exposed (50). Detailed discussion on the surgical anatomy of the endoscopic approaches is beyond the scope of this piece, and the reader is referred to the many available excellent studies (47, 51, 52).

Conclusion
A detailed understanding of the MCF microanatomy is required to successfully navigate it without complications. The present review tries to encompass most of the relevant neurovascular anatomic nuances that are of practical significance when approaching the MCF. It should be noted, however, that the surgical approaches need to be studied and practiced in a cadaver lab to maximize the application of the anatomic facts during surgery. Also, many pathologic states alter the normal anatomical relationships and, therefore, each surgical approach has to be specifically tailored to the individual patient pathoanatomy.

Author contributions
ATM: conception and design, data collection, article drafting, critical review, review on behalf of all authors, and study supervision. GM-J: data collection, article drafting, critical review. MTL: data collection, critical review. JKL: data collection, critical review. MCP: data collection, critical review. HS: data collection, critical review, and study supervision. All authors contributed to the article and approved the submitted version.