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Trigeminal nerve

The trigeminal nerve, designated as the fifth cranial nerve (CN V), is the largest of the twelve cranial nerves and functions as a mixed sensory and motor nerve, primarily providing sensory innervation to the face, mouth, and anterior scalp while delivering motor impulses to the muscles involved in mastication.^[1] It originates from the lateral pons and consists of a large sensory root (portio major) and a smaller motor root (portio minor). The sensory root enters the trigeminal ganglion in the Meckel cave, while the motor root passes beneath the ganglion to join the mandibular division.^[1] The nerve divides into three main branches—ophthalmic (V1), maxillary (V2), and mandibular (V3)—each exiting the skull through distinct foramina to supply specific regions of the head.^[1] Structurally, the trigeminal nerve's sensory components transmit sensations of touch, pain, and temperature from the face via three primary nuclei: the principal sensory nucleus for discriminative touch, the spinal trigeminal nucleus for pain and temperature, and the mesencephalic nucleus for proprioception from the jaw muscles.^[1] The motor root, embedded within the mandibular division, innervates key muscles of mastication including the masseter, temporalis, lateral and medial pterygoids, as well as the mylohyoid, anterior belly of the digastric, and tensor veli palatini and tympani.^[2] Embryologically, it derives from the first branchial arch, with the ganglion forming around the 26th day of development and nuclei appearing by the 33rd day.^[1] Blood supply to the nerve and ganglion arises mainly from the cavernous segment of the internal carotid artery, middle meningeal artery, and branches of the basilar and cerebellar arteries.^[1] Clinically, the trigeminal nerve plays a critical role in reflexes such as the corneal reflex (afferent limb for bilateral eyelid closure) and the jaw-jerk reflex (testing motor integrity via a tap on the chin).^[1] Dysfunction often manifests as trigeminal neuralgia, characterized by severe, paroxysmal facial pain triggered by minor stimuli, frequently due to vascular compression by the superior cerebellar artery; treatment may involve medications like carbamazepine or surgical interventions such as microvascular decompression.^[1] Lesions can also lead to facial hypesthesia, anesthesia, or motor deficits like jaw deviation toward the affected side, and the nerve's involvement extends to conditions like cluster headaches and lateral medullary syndrome.^[2]

Anatomy

Origin and course

The trigeminal nerve (cranial nerve V) originates from the anterolateral surface of the mid-pons in the brainstem, where it emerges as two distinct roots: a large sensory root, known as the portio major, and a smaller motor root, the portio minor. The sensory root consists of central processes from pseudounipolar neurons in the trigeminal ganglion, while the motor root arises from motor neurons in the pontine tegmentum.^[1]^[2] From its pontine origin, the trigeminal nerve exits the brainstem at the level of the middle cerebellar peduncle and courses anteriorly through the posterior cranial fossa, traversing the prepontine and cerebellopontine angle cisterns. During this intracranial segment, the nerve lies in close proximity to the superior cerebellar artery, which arises from the basilar artery and courses superiorly adjacent to the trigeminal root entry zone. The overall length of the nerve from the pons to the trigeminal ganglion measures approximately 12 mm, marking the transition from central to peripheral myelin at the root entry zone.^[1]^[3] The undivided trigeminal trunk then pierces the dura mater via the porus trigeminus to enter Meckel's cave, a CSF-filled dural pouch located at the petrous apex of the temporal bone and formed by an invagination of the tentorium cerebelli. Within this cave, the sensory root attaches to the trigeminal ganglion, the site of cell bodies for the nerve's pseudounipolar sensory neurons, while the motor root passes beneath the ganglion to join the mandibular division. Laterally, the nerve relates to the internal carotid artery as it approaches the petrous apex.^[1]^[2]^[4]

Trigeminal ganglion

The trigeminal ganglion, also known as the semilunar or Gasserian ganglion, serves as the primary sensory relay for the trigeminal nerve (cranial nerve V), housing the cell bodies of its sensory neurons. It is situated within Meckel's cave, a dural invagination on the petrous apex of the temporal bone, surrounded by cerebrospinal fluid and layers of the arachnoid membrane for protection.^[1]^[5] This ganglion is a thin, crescent-shaped structure composed primarily of pseudounipolar sensory neuron cell bodies, with estimates indicating approximately 20,000 to 35,000 neurons in humans.^[6]^[7] The sensory root of the trigeminal nerve, originating from the pons, enters the ganglion, from which three major divisions emerge: the superior ophthalmic division (V1), the middle maxillary division (V2), and the inferior mandibular division (V3).^[8] Additionally, the ganglion receives sympathetic fibers from the internal carotid plexus, which traverse its vicinity.^[9] In clinical contexts, the trigeminal ganglion is a key anatomical target for percutaneous rhizotomy procedures, such as radiofrequency ablation, to interrupt pain transmission in cases of trigeminal neuralgia.^[10]

Ophthalmic division

The ophthalmic division (V1) of the trigeminal nerve is the smallest and uppermost of its three sensory branches, arising from the anterosuperior aspect of the trigeminal ganglion located in Meckel's cave.^[1] It courses anteriorly along the lateral wall of the cavernous sinus, positioned lateral to the abducens nerve (CN VI) and inferior to the oculomotor (CN III) and trochlear (CN IV) nerves, before exiting the cranium through the superior orbital fissure to enter the orbit.^[1]^[11] Within the orbit, it divides into three terminal branches—frontal, lacrimal, and nasociliary—near the orbital apex, providing general somatic afferent innervation to the upper face, orbit, and anterior meninges.^[1]^[11] Additionally, it conveys sympathetic fibers from the internal carotid plexus, which contribute to pupillary dilation via the long ciliary nerves.^[1] The frontal nerve, the largest branch, travels superiorly between the periosteum and levator palpebrae superioris muscle before bifurcating into the supraorbital and supratrochlear nerves.^[11] The supraorbital nerve exits the orbit through the supraorbital foramen, supplying sensory innervation to the skin of the forehead, scalp as far as the vertex, upper eyelid, and mucosa of the frontal sinus.^[11] The supratrochlear nerve emerges medial to the supraorbital notch, providing sensation to the medial upper eyelid, lower forehead, and skin over the root of the nose.^[11] The lacrimal nerve courses superiorly along the lateral rectus muscle to reach the lacrimal gland, where it delivers sensory fibers to the gland itself and the adjacent conjunctiva and skin of the lateral upper eyelid.^[11] It also carries parasympathetic secretomotor fibers (originating from the facial nerve via the pterygopalatine ganglion) that stimulate lacrimal secretion.^[11] The nasociliary nerve arcs forward across the optic nerve (CN II), giving rise to several key branches: the long ciliary nerves (three to five), which pierce the sclera to innervate the cornea, iris, and ciliary body; the infratrochlear nerve, supplying the skin of the medial upper eyelid, lacrimal sac, and side of the nose, as well as the conjunctiva; the anterior ethmoidal nerve, which innervates the anterior ethmoidal air cells, frontal sinus mucosa, and anterosuperior nasal septum; the posterior ethmoidal nerve, targeting the posterior ethmoidal air cells and sphenoidal sinus mucosa; and a meningeal branch that provides sensory supply to the dura mater of the anterior cranial fossa.^[1]^[11] Overall, the ophthalmic division ensures sensory coverage of the cornea, conjunctiva, nasal mucosa, external nose, upper eyelid skin, and associated sinuses.^[1]^[11] In its orbital course, the ophthalmic division travels in close proximity to the oculomotor, trochlear, and abducens nerves, as well as the ophthalmic artery and superior ophthalmic vein, within the annulus of Zinn or adjacent structures at the superior orbital fissure.^[12] Its blood supply derives from branches of the ophthalmic artery, which accompanies it through the orbit.^[11]

Maxillary division

The maxillary division, also known as the second division of the trigeminal nerve (V2), is the intermediate sensory branch arising from the anterior convexity of the trigeminal ganglion, positioned between the ophthalmic and mandibular divisions.^[13] It courses forward along the lateral wall of the cavernous sinus, exits the skull through the foramen rotundum into the pterygopalatine fossa, and then continues as the infraorbital nerve, passing through the inferior orbital fissure, infraorbital groove and canal, before emerging onto the face via the infraorbital foramen.^[13] This pathway allows V2 to provide sensory innervation to the midfacial structures without any motor components.^[1] In the pterygopalatine fossa, the maxillary nerve gives off several key branches before becoming the infraorbital nerve. These include the zygomatic nerve (which further divides into zygomaticotemporal and zygomaticofacial branches), pterygopalatine nerves (communicating with the pterygopalatine ganglion and distributing as posterior superior alveolar, greater and lesser palatine, nasopalatine, and pharyngeal branches), and meningeal branches to the dura.^[13] The infraorbital nerve then provides the middle and anterior superior alveolar branches within the orbit and infraorbital canal, followed by terminal branches on the face: inferior palpebral, lateral nasal, and superior labial nerves.^[13] The maxillary division innervates a range of midfacial and intraoral structures, including the skin of the lower eyelid, side of the nose, cheek, and upper lip; the maxillary sinus; the nasal cavity and nasopharynx; the palate; and the upper teeth and gums.^[13] It also supplies the dura mater of the middle cranial fossa via its meningeal branches and indirectly influences lacrimal gland secretion through parasympathetic fibers carried via the zygomatic branch.^[13] Anatomically, the maxillary nerve lies inferior to the ophthalmic division in the cavernous sinus and is closely associated with the pterygopalatine ganglion in the fossa, where it receives parasympathetic and sympathetic fibers for distribution to target glands and mucosa.^[13] The maxillary artery runs parallel and adjacent to it in the pterygopalatine fossa, facilitating vascular support.^[13] Blood supply to the maxillary nerve derives proximally from the superolateral and inferolateral pontine arteries at the pons level, as well as branches from the anterior inferior cerebellar artery; more distally, in the middle cranial fossa, it receives contributions from the artery of the foramen rotundum and middle meningeal artery, while in the pterygopalatine fossa, branches of the maxillary artery provide nourishment.^[13]

Mandibular division

The mandibular division, also known as the third division or V3 of the trigeminal nerve, is the largest and most caudal branch of the trigeminal nerve, characterized by its mixed sensory and motor composition.^[14] It provides general somatic afferent innervation to the lower face, oral cavity, and temporomandibular joint (TMJ), while its motor component supplies the muscles of mastication and other associated structures.^[1] Unlike the purely sensory ophthalmic (V1) and maxillary (V2) divisions, V3 integrates motor fibers from the trigeminal motor root, which join it proximal to the skull base.^[14] The mandibular division originates from the trigeminal ganglion within Meckel's cave and exits the skull through the foramen ovale, entering the infratemporal fossa where it divides into a smaller anterior trunk (primarily motor with some sensory fibers) and a larger posterior trunk (predominantly sensory).^[1] In the infratemporal fossa, the nerve lies medial to the lateral pterygoid muscle and superior to the medial pterygoid, facilitating its access for regional nerve blocks used in dental and maxillofacial procedures.^[14] This course positions V3 in close relation to the otic ganglion, through which parasympathetic fibers from the glossopharyngeal nerve (via lesser petrosal nerve) hitchhike to reach the parotid gland, while sympathetic fibers from the internal carotid plexus also travel along its branches.^[1] The sensory branches arise mainly from the posterior trunk and provide cutaneous and mucosal innervation to the lower face and oral structures. The auriculotemporal nerve emerges by duplication around the middle meningeal artery, ascending to supply the external acoustic meatus, tympanic membrane, auricle, and skin of the temple, as well as sensory input from the TMJ and parotid fascia.^[14] The buccal nerve courses anteriorly between the two pterygoid heads to innervate the skin, mucosa, and gingiva of the cheek and buccal sulcus.^[1] The lingual nerve descends medial to the mandible, providing general sensation to the anterior two-thirds of the tongue, floor of the mouth, and lingual gingiva; it joins with the chorda tympani (a branch of the facial nerve) just below the mandible to convey taste fibers and parasympathetic innervation to the submandibular and sublingual glands.^[14] The inferior alveolar nerve, the largest sensory branch, travels within the pterygomandibular space to enter the mandibular canal via the mandibular foramen, supplying the lower teeth and adjacent gingiva before terminating as the mental nerve, which emerges through the mental foramen to innervate the skin of the chin and lower lip.^[1] Motor branches primarily stem from the anterior trunk and innervate the primary muscles involved in mastication and related functions, ensuring coordinated jaw movement with sensory feedback from the same division. These include deep branches to the medial and lateral pterygoid muscles, a nerve to the masseter that pierces the mandibular notch, and the masseteric nerve to the temporalis muscle via its deep surface.^[14] Additional motor fibers supply the mylohyoid and anterior belly of the digastric muscles via a submandibular branch, as well as the tensor veli palatini and tensor tympani muscles through communications with the otic ganglion.^[1] Overall, V3's sensory targets encompass the lower lip, chin, anterior tongue, lower teeth, TMJ, and external ear, integrating proprioceptive input from masticatory muscles to facilitate precise oral motor control.^[14]

Motor root

The motor root of the trigeminal nerve, also known as portio minor, originates from neurons in the trigeminal motor nucleus located in the lateral aspect of the pontine tegmentum.^[1] These fibers emerge from the anterolateral surface of the mid-pons, exiting the brainstem immediately lateral to the larger sensory root.^[15] Unlike the sensory root, the motor root does not synapse in the trigeminal ganglion but passes through it without interruption.^[1] The motor root travels alongside the sensory root through the prepontine and cerebellopontine angle cisterns, entering the trigeminal cave (Meckel's cave) where it combines with the sensory fibers of the mandibular division (V3).^[1] It does not traverse a dedicated foramen but exits the skull base with V3 through the foramen ovale into the infratemporal fossa, where it distributes its branches.^[14] The motor root joins the mandibular division (V3) after passing beneath the trigeminal ganglion within Meckel's cave.^[16] The motor root provides no sensory innervation itself, though proprioceptive fibers from masticatory muscle spindles are conveyed separately via the mesencephalic nucleus of the trigeminal nerve.^[1] Its branches, arising primarily from the mandibular division in the infratemporal fossa, include deep temporal nerves (anterior and posterior), masseteric nerve, nerves to the lateral and medial pterygoid muscles, mylohyoid nerve, and nerves to the tensor veli palatini and tensor tympani muscles.^[17]^[15] These branches exclusively innervate the muscles of mastication—masseter, temporalis, medial pterygoid, and lateral pterygoid—as well as accessory muscles including the anterior belly of the digastric, mylohyoid, tensor veli palatini, and tensor tympani.^[1]^[2] The deep temporal nerves supply the temporalis muscle, the masseteric nerve targets the masseter, the pterygoid nerves innervate their respective pterygoid muscles, and the mylohyoid nerve serves the mylohyoid and anterior digastric, while the tensor nerves reach their palatal and tympanic targets.^[17] This distribution supports special visceral efferent (SVE) function derived from the first pharyngeal arch.^[15]

Function

Sensory innervation

The trigeminal nerve (cranial nerve V) provides general somatic afferent innervation to the face and anterior head, conveying sensations of touch (mechanoreception), pain (nociception), temperature (thermoreception), and proprioception from muscles and joints.^[1] These modalities are mediated through its three primary divisions: ophthalmic (V1), maxillary (V2), and mandibular (V3). Proprioceptive fibers specifically arise from structures such as the hard palate, teeth, periodontium, temporomandibular joint (TMJ), extraocular muscles, and masticatory muscles.^[1] The sensory dermatomes of the trigeminal nerve correspond to its divisions, with V1 covering the forehead, scalp, orbit, and nose; V2 innervating the cheek, upper lip, side of nose, and lower eyelid; and V3 supplying the lower jaw, chin, temple, and anterior ear.^[1] These dermatomes exhibit minimal overlap among themselves but intersect with cervical dermatomes C2 and C3, particularly at the angle of the jaw, where great auricular nerve contributions from the cervical plexus provide additional sensation.^[18] Key innervated structures include the skin of the face (excluding the angle of the jaw), mucosa of the oral, nasal, and pharyngeal cavities, teeth, meninges, cornea, TMJ, and paranasal sinuses.^[1] The cornea stands out as the most densely innervated surface in the body, with approximately 7,000 nociceptors per square millimeter—300 to 600 times denser than skin innervation—making it highly sensitive to protective stimuli.^[19] Special sensory functions involve the corneal reflex arc, where afferent signals from corneal touch travel via the V1 division to elicit bilateral eyelid closure through efferent facial nerve (cranial nerve VII) pathways.^[1] Referred pain patterns are common, such as maxillary sinus inflammation projecting pain to the upper teeth due to shared V2 innervation.^[20]

Motor innervation

The motor innervation of the trigeminal nerve arises from its motor root, which joins the mandibular division (CN V3) to supply efferent fibers to the muscles involved in mastication.^[1] This component originates from the trigeminal motor nucleus in the pontine tegmentum and provides somatic motor innervation exclusively through V3, enabling precise control of jaw movements essential for chewing and related oral functions.^[21] The primary muscles innervated include the masseter, which elevates the mandible and contributes to protrusion via its superficial fibers; the temporalis, responsible for elevation and retraction; the medial pterygoid, which elevates, protrudes, and facilitates side-to-side grinding movements; and the lateral pterygoid, which depresses the jaw, protrudes it, and supports lateral excursions.^[21] These muscles work in concert to generate the forces required for biting and grinding food, with human incisor bite forces typically ranging from 168 to 208 N, reflecting the coordinated action of these elevators and depressors.^[22] Accessory muscles supplied by V3 branches include the mylohyoid, which elevates the floor of the mouth and depresses the mandible; the anterior belly of the digastric, aiding in jaw depression; the tensor veli palatini, which tenses the soft palate and opens the Eustachian tube; and the tensor tympani, which dampens middle ear vibrations.^[1] These contribute to auxiliary actions during mastication, such as stabilizing the hyoid and palate for efficient swallowing integration. Bilateral activation of the primary muscles ensures symmetrical jaw closure and elevation for routine chewing, while unilateral contraction, particularly of the pterygoids, enables lateral grinding movements to process food on one side.^[21] This coordination with the facial nerve (CN VII), which innervates muscles like the buccinator for maintaining oral competence during chewing, prevents food spillage and supports overall masticatory efficiency.^[2] Clinically, weakness in trigeminal motor innervation, often due to V3 lesions, manifests as impaired jaw strength and deviation toward the affected side upon opening, primarily from lateral pterygoid involvement, leading to difficulties in chewing and asymmetrical bite force.^[23]

Reflexes and proprioception

The trigeminal nerve plays a key role in several protective reflexes involving the face, mouth, and upper airway. The jaw jerk reflex, a monosynaptic stretch reflex, is elicited by tapping the chin with the mouth slightly open, resulting in a brief upward movement of the jaw due to contraction of the masseter and temporalis muscles.^[24] This reflex arc involves proprioceptive afferents from muscle spindles traveling via the mandibular division (V3) to the mesencephalic nucleus, synapsing directly with motor neurons in the trigeminal motor nucleus to produce jaw closure.^[1] In healthy individuals, the response is typically slight or absent, but it becomes exaggerated in upper motor neuron lesions affecting the corticobulbar tract, while it is diminished or absent in peripheral trigeminal lesions or nuclear damage.^[24]^[2] The corneal reflex protects the eye by triggering a bilateral blink in response to corneal stimulation, such as by a cotton wisp. The afferent limb is carried by the ophthalmic division (V1) through the nasociliary nerve to the spinal trigeminal nucleus, while the efferent limb involves the facial nerve (VII) innervating the orbicularis oculi muscle.^[25] This disynaptic reflex has an early ipsilateral component mediated by A-beta fibers and a late bilateral component involving secondary interneurons, with absence indicating ipsilateral trigeminal or facial nerve dysfunction and bilateral absence suggesting brainstem involvement.^[25]^[24] Other trigeminal-mediated reflexes include the sneeze reflex, triggered by nasal mucosa irritation via the ophthalmic division (V1) afferents from the anterior ethmoidal nerve, which activate brainstem centers to produce explosive expiration.^[26] The gag reflex, with primary sensory input from the glossopharyngeal nerve (IX) for soft palate stimulation, provides afferents to the spinal trigeminal and solitary nuclei, with efferents primarily from the glossopharyngeal (IX) and vagus (X) nerves causing pharyngeal constriction.^[27] Proprioception from the trigeminal nerve enables unconscious monitoring of jaw position and movement, primarily through primary afferent neurons whose cell bodies are uniquely located in the mesencephalic nucleus rather than a peripheral ganglion. These neurons receive input from muscle spindles in the masticatory muscles (masseter, temporalis, and pterygoids), the temporomandibular joint capsule, and periodontal ligaments around the teeth.^[28]^[1] This proprioceptive feedback facilitates precise adjustments in bite force during mastication by modulating motor output to prevent excessive pressure on teeth and joints.^[2] Clinically, disruption of these pathways, as in trigeminal neuropathy, can impair jaw coordination and lead to abnormal reflexes, such as an absent jaw jerk, highlighting the nerve's role in maintaining oral motor integrity.^[29]

Central connections

Principal sensory nucleus

The principal sensory nucleus of the trigeminal nerve, also referred to as the chief or main sensory nucleus, is situated in the mid-pons within the lateral tegmentum, positioned posterolateral to the trigeminal motor nucleus and dorsomedial to the entering trigeminal root fibers.^[28] This nucleus receives primary afferent fibers from the trigeminal ganglion via short collaterals of the principal sensory root, which bypass the spinal trigeminal tract.^[30] It lies caudal to the mesencephalic nucleus and rostral to the spinal trigeminal nucleus, forming part of the trigeminal sensory complex in the brainstem.^[1] The primary function of the principal sensory nucleus is to process discriminative somatosensory information, including fine touch, vibration, two-point discrimination, and conscious proprioception from the ipsilateral face, oral cavity, and associated structures such as the temporomandibular joint.^[28] This processing enables precise localization and discrimination of tactile stimuli on the face and in the mouth, analogous to the role of the dorsal column nuclei and medial lemniscus pathway in conveying similar sensations from the rest of the body.^[1] Unlike broader somatosensory integration, the nucleus emphasizes high-acuity tactile discrimination essential for oral manipulation and facial sensation.^[31] Afferent inputs to the nucleus arise mainly from the maxillary (V2) and mandibular (V3) divisions of the trigeminal nerve, particularly for oral cavity structures, which project to the dorsomedial subdivision; the ophthalmic (V1) division contributes to a lesser extent, targeting the ventrolateral subdivision alongside inputs from V2 and V3.^[31] The organization is predominantly ipsilateral, with primary neurons synapsing directly in the nucleus after traversing the pons.^[28] Somatotopically, the nucleus maps the head in an orderly fashion, with rostral regions in the dorsomedial part representing the oral cavity and teeth, while ventrolateral areas correspond to cutaneous facial regions, reflecting the peripheral innervation patterns of the trigeminal divisions.^[32] Efferent projections from second-order neurons in the principal sensory nucleus form the trigeminothalamic tracts, conveying processed tactile information to higher centers; the ventrolateral portion contributes to the ventral trigeminothalamic tract (also termed the quintothalamic tract), which decussates and ascends contralaterally to the ventral posteromedial (VPM) nucleus of the thalamus, while the dorsomedial portion projects ipsilaterally via the dorsal trigeminothalamic tract to the same thalamic target.^[28] These pathways ultimately relay to the primary somatosensory cortex for conscious perception of facial touch.^[1]

Spinal trigeminal nucleus

The spinal trigeminal nucleus is a columnar collection of neurons located in the dorsolateral brainstem that extends rostrocaudally from the level of the caudal pons through the medulla oblongata and into the upper cervical spinal cord, typically reaching segments C1 to C3.^[33] This structure runs parallel and medial to the spinal trigeminal tract, forming a continuous extension of the dorsal horn of the spinal cord.^[1] It serves as the primary central relay for processing nociceptive and thermoreceptive information from the ipsilateral face and anterior head.^[34] The nucleus is subdivided into three main regions along its rostrocaudal axis: the pars oralis, pars interpolaris, and pars caudalis. The pars oralis occupies the rostral portion in the mid-pons to the upper medulla, receiving inputs primarily related to non-noxious mechanical stimuli from intraoral structures and contributing to brainstem reflexes such as the jaw-opening reflex.^[33] The pars interpolaris, located in the middle third of the medulla between the rostral inferior olive and the obex, acts as a transitional zone that modulates sensory inputs from the anterior face, including contributions to the anterior trigeminothalamic tract for initial pain processing.^[1] The pars caudalis, the most caudal subdivision extending from the obex into the upper cervical cord, contains wide-dynamic-range neurons that are crucial for integrating and modulating sharp and dull pain as well as temperature sensations from the face.^[34] Primary afferent inputs to the spinal trigeminal nucleus arise from small-diameter myelinated (Aδ) and unmyelinated (C) fibers of the trigeminal ganglion, carrying nociceptive and thermoreceptive signals from all three divisions of the trigeminal nerve (ophthalmic, maxillary, and mandibular).^[33] These fibers descend ipsilaterally in the spinal trigeminal tract before synapsing in the nucleus, with additional inputs from cranial nerves VII, IX, and X via their respective ganglia for sensations from the ear, pharynx, and meninges.^[34] The nucleus exhibits a somatotopic organization resembling an "onion-skin" lamination, where perioral and intraoral regions (V3) are represented in the more rostral and dorsal parts, while peripheral facial areas (V1 and V2) map to caudal and ventral layers, allowing for layered processing of facial pain distribution.^[33] Outputs from the spinal trigeminal nucleus primarily involve second-order neurons that decussate and ascend contralaterally via the ventral and dorsal trigeminothalamic tracts—analogous to the spinothalamic pathway—to terminate in the ventral posteromedial nucleus of the thalamus, ultimately relaying to the somatosensory cortex for conscious perception of pain and temperature.^[1] Local interneurons within the nucleus facilitate short-range connections for spinal reflexes, while projections from the pars caudalis also target supraspinal sites such as the periaqueductal gray for pain modulation.^[34]

Mesencephalic nucleus

The mesencephalic nucleus of the trigeminal nerve is a distinctive sensory nucleus situated within the central nervous system, extending longitudinally from the level of the superior colliculus in the caudal midbrain (mesencephalon) through the rostral pons, reaching as far as the vicinity of the locus coeruleus.^[1]^[28] This elongated column of neurons lies adjacent to the periaqueductal gray matter and the cerebral aqueduct, making it unique among brainstem nuclei for housing primary sensory cell bodies directly in the CNS rather than in a peripheral ganglion like the trigeminal ganglion.^[28] Structurally, the nucleus comprises pseudounipolar neurons resembling those of dorsal root ganglia, with cell bodies that give rise to peripheral processes innervating peripheral receptors and central processes that descend ipsilaterally along the mesencephalic tract of the trigeminal nerve.^[1] These primary afferent neurons do not synapse within the nucleus itself; instead, their central axons continue caudally without interruption to target downstream structures.^[28] The peripheral processes originate mainly from the mandibular division (V3) of the trigeminal nerve, conveying proprioceptive inputs from specialized receptors in the orofacial region.^[1] The primary function of the mesencephalic nucleus is to transmit unconscious proprioceptive signals essential for masticatory coordination, including jaw position awareness and regulation of bite force.^[28] It receives inputs from muscle spindles in the masticatory muscles (such as the masseter, temporalis, and pterygoids), the temporomandibular joint (TMJ) capsule, periodontal ligaments surrounding the teeth, and Golgi tendon organs within these muscles.^[1] These afferents provide feedback on muscle stretch, joint movement, and dental occlusion, supporting reflexive adjustments during chewing and preventing excessive force that could damage teeth or tissues.^[28] Central projections from the mesencephalic nucleus include direct, monosynaptic connections to the ipsilateral trigeminal motor nucleus, facilitating rapid motor responses to proprioceptive input.^[1] Some neurons also send collaterals to the cerebellum, contributing to fine-tuning of orofacial motor control through cerebello-trigeminal pathways.^[35] This organization underpins the jaw-jerk reflex, where stretch of masticatory muscles elicits a brisk contraction via the mesencephalic-motor loop.^[28]

Pathways to thalamus and cortex

The ascending sensory pathways of the trigeminal nerve convey information from the brainstem nuclei to higher centers for processing tactile, proprioceptive, nociceptive, and thermal sensations from the face and oral cavity. Second-order neurons from the principal sensory nucleus and spinal trigeminal nucleus primarily decussate in the pons or medulla and ascend contralaterally via the quintothalamic tract (also known as the trigeminal lemniscus) to terminate in the ventral posteromedial (VPM) nucleus of the contralateral thalamus.^[30]^[2] A smaller proportion of fibers from the principal sensory nucleus ascends ipsilaterally, contributing to bilateral representation, particularly for oral structures.^[2] In the thalamus, third-order neurons in the VPM nucleus relay this information via thalamocortical radiations through the posterior limb of the internal capsule to the primary somatosensory cortex (S1) in the postcentral gyrus, corresponding to Brodmann areas 3, 1, and 2, where precise localization of facial sensations occurs.^[1]^[30] Projections also extend to the secondary somatosensory cortex (S2) in the upper bank of the lateral sulcus for further sensory integration and to the insular cortex, which modulates the affective and emotional components of pain.^[36] For nociceptive signals, additional pathways from the spinal trigeminal nucleus involve the spinoreticular tract, projecting to reticular formation nuclei to influence arousal and autonomic responses before thalamic relay.^[30] Somatotopic organization is maintained throughout these pathways: the face is represented in the lateral portion of the VPM nucleus, with perioral regions occupying a disproportionately large area, and this map is preserved in the cortical homunculus of S1, where the mouth and lips receive extensive representation relative to other facial areas.^[1]^[2] This organization enables fine-grained discrimination of sensory inputs, such as touch on the lips versus the forehead.^[30]

Development and variations

Embryology

The sensory components of the trigeminal nerve arise from a combination of neural crest cells and cells derived from the trigeminal placode, a specialized region of neurogenic ectoderm, while the motor neurons originate from the basal plate of the embryonic hindbrain.^[37]^[38]^[39] Neural crest cells delaminate from the dorsal neural tube at the midbrain-hindbrain junction and migrate ventrally, intermingling with placode-derived neuroblasts to form the trigeminal ganglion.^[40] This dual origin ensures the nerve's sensory neurons innervate diverse craniofacial structures, with placodal contributions primarily forming ophthalmic trigeminal neurons.^[37] Development begins around the 4th week of gestation (Carnegie stage 12, approximately 26–30 days), when the trigeminal ganglion first emerges as a condensation of migrating neural crest cells and placodal cells near the first pharyngeal arch.^[38]^[41] By the 5th week (stage 14, 31–35 days), the three primary divisions—ophthalmic, maxillary, and mandibular—begin to differentiate as neural crest populations invade specific mesenchymes.^[41] The ganglion achieves a more defined structure by the 6th week, with ongoing placodal contributions, and the divisions elongate and branch fully by the 8th week (around 56 days), establishing connections to target tissues.^[41]^[38] Neural crest cells from the midbrain region migrate to the frontonasal prominence, contributing to the ophthalmic and maxillary divisions, while hindbrain-derived crest cells populate the first branchial arch to form the mandibular division's mesenchyme and innervation.^[42]^[43] This targeted migration is guided by molecular cues, including the transcription factor Pax3, which marks early placodal ectoderm and supports ganglion formation; Hoxa2, which patterns branchial arch derivatives; and FGF8 signaling, which specifies branch identities and promotes neural crest survival and differentiation.^[44]^[45]^[46] Disruptions in these early processes, such as impaired neural crest migration or placode induction, can result in congenital anomalies like aglossia-adactyly syndrome, characterized by absence of the tongue and limb defects due to first arch malformations.^[47]

Anatomical variations

The trigeminal nerve exhibits considerable anatomical variability, both congenital and acquired, which can influence surgical approaches, nerve blocks, and diagnostic imaging. Congenital variations primarily affect the branching patterns and communications between divisions, with high prevalence in inter-branch connections that may alter sensory distribution. For instance, communications between the ophthalmic (V1) and maxillary (V2) divisions can occur via connections between the lacrimal nerve (V1) and zygomatic nerve (V2), potentially carrying parasympathetic fibers and leading to overlapping innervation in the orbital region.^[9] Specific congenital variants include accessory branches, such as sensory fibers in the mylohyoid nerve (a branch of V3), reported in 20-60% of cases, providing supplementary innervation to the mandibular teeth, chin skin, and lower incisors.^[48] Duplication of the trigeminal (Gasserian) ganglion is extremely rare, known primarily from case reports and sometimes associated with persistent primitive vessels like the trigeminal artery (prevalence approximately 0.3-0.4%). Variants related to the foramen ovale, such as duplication or accessory foramina, occur in 2-30% of cases and may lead to early division of the mandibular division (V3), complicating access during procedures like microvascular decompression. These variations arise from embryonic neural crest migration but are not tied to broader developmental anomalies.^[49]^[50] Acquired changes often involve external compression or pathological encroachment. Neurovascular compression, particularly at the root entry zone by arteries like the superior cerebellar artery, occurs in 10-30% of asymptomatic individuals but rises to 70-95% in symptomatic cases of trigeminal neuralgia (TN).^[51] Tumors like schwannomas or meningiomas can distort nerve branches, accounting for approximately 3-6% of secondary TN cases and altering the nerve's trajectory.^[52] Blood supply variations to the trigeminal nerve and ganglion derive primarily from the cavernous segment of the internal carotid artery and middle meningeal artery, but accessory contributions from the ophthalmic or maxillary arteries occur in up to 30% of cases, potentially increasing vulnerability to ischemia during interventions. Lymphatic drainage consistently follows the nerve branches to the deep cervical nodes, with minimal reported variability.^[1] Magnetic resonance imaging (MRI), particularly high-resolution sequences like FIESTA or CISS, effectively visualizes these variants, detecting branch communications, ganglion anomalies, and compressions with sensitivity exceeding 90%, guiding precise nerve blocks and surgical planning.^[53]

Clinical significance

Trigeminal neuralgia

Trigeminal neuralgia, also known as tic douloureux, is a chronic neuropathic pain disorder defined by sudden, recurrent episodes of severe, unilateral, electric shock-like pain confined to the distribution of one or more branches of the trigeminal nerve, most commonly the maxillary (V2) or mandibular (V3) divisions.^[54] The pain attacks typically last from a few seconds to two minutes, with intervals of complete relief between paroxysms, and may occur in clusters over days or weeks followed by periods of remission.^[55] This condition primarily affects the sensory components of the trigeminal nerve, leading to intense discomfort without motor involvement.^[56] Epidemiologically, trigeminal neuralgia has an annual incidence of 4 to 13 cases per 100,000 individuals, with a lifetime prevalence estimated at 0.16% to 0.3%.^[54] It predominantly occurs in individuals over 50 years of age, with a peak incidence between 50 and 60 years, and shows a female-to-male ratio of approximately 2:1 to 3:1.^[56] About 90% of cases are classified as classical trigeminal neuralgia, while the remaining 10% are symptomatic, often secondary to underlying conditions such as multiple sclerosis.^[55] The pathophysiology of classical trigeminal neuralgia centers on neurovascular compression of the trigeminal nerve root entry zone, most frequently by the superior cerebellar artery in 75% to 90% of cases, resulting in focal demyelination.^[54] This demyelination lowers the threshold for nerve excitation and promotes ephaptic transmission, where aberrant electrical cross-talk between adjacent nerve fibers generates ectopic impulses and paroxysmal pain.^[55] In symptomatic cases, structural lesions like tumors or demyelinating plaques disrupt normal trigeminal sensory conduction similarly.^[56] Common triggers for pain attacks include innocuous stimuli such as light touch to the face, chewing, talking, brushing teeth, or exposure to cold wind, often arising from specific trigger zones like the perioral or nasolabial regions.^[54] These episodes can be exacerbated by non-noxious mechanical or thermal inputs, with many patients experiencing both triggered and spontaneous attacks, and remission phases that may last months to years.^[56] Variants of trigeminal neuralgia include the classical form, which is purely paroxysmal, and atypical trigeminal neuralgia, characterized by a constant burning or aching pain superimposed on the shock-like episodes in about 14% to 50% of cases.^[55] Bilateral involvement is rare, occurring in approximately 3% of patients and frequently associated with multiple sclerosis.^[56]

Other neuropathies and syndromes

Postherpetic neuralgia involving the trigeminal nerve typically arises following reactivation of varicella-zoster virus in the ophthalmic division (V1), resulting in herpes zoster ophthalmicus. This condition manifests as persistent, constant burning pain in the affected facial dermatomes, often accompanied by allodynia and hyperalgesia, persisting beyond three months after the acute rash resolves. The incidence of postherpetic neuralgia after trigeminal herpes zoster ranges from 10% to 20%, with higher rates associated with ophthalmic involvement due to the dense innervation of the V1 distribution.^[57]^[58]^[59] The trigeminal nerve is also implicated in cluster headaches, a type of trigeminal autonomic cephalalgia characterized by severe unilateral pain in the ophthalmic (V1) distribution, often around the eye, accompanied by autonomic symptoms like lacrimation and nasal congestion. Episodes are short (15-180 minutes) and occur in clusters, with a lifetime prevalence of about 0.1%.^[54] Trigeminal neuropathy encompasses a range of disorders characterized primarily by sensory loss or dysfunction in the trigeminal nerve distributions, often without the paroxysmal pain seen in neuralgia. Trauma, such as from facial injuries or surgical interventions, can directly damage the nerve peripherally, leading to unilateral hypoesthesia or anesthesia in the affected divisions. Systemic autoimmune conditions like Sjögren's syndrome frequently cause trigeminal sensory neuropathy through mechanisms including vasculitis or axonal degeneration, presenting with numbness or paresthesia that may precede other systemic symptoms. Similarly, sarcoidosis can involve the trigeminal nerve via granulomatous infiltration, resulting in isolated or multifocal neuropathy with facial sensory deficits; in systemic cases, involvement is often bilateral, reflecting widespread neuroinflammatory processes.^[29]^[60]^[61] Central syndromes affecting the trigeminal pathway arise from lesions in the brainstem nuclei or tracts, disrupting sensory processing. In Wallenberg syndrome, or lateral medullary syndrome, infarction of the dorsolateral medulla typically causes ipsilateral facial pain and loss of temperature sensation due to involvement of the spinal trigeminal nucleus and tract, often alongside contralateral body deficits from spinothalamic tract damage. Multiple sclerosis can produce similar trigeminal symptoms through demyelinating plaques in the principal sensory nucleus, spinal trigeminal nucleus, or root entry zone, leading to chronic facial dysesthesias or sensory loss that correlates with lesion location on neuroimaging.^[62]^[63] Tumors impacting the trigeminal nerve include both primary and secondary neoplasms that compress or infiltrate neural structures. Trigeminal schwannomas are benign, encapsulated tumors originating from Schwann cells along the nerve root, ganglion, or peripheral branches, characterized by slow growth that may erode adjacent bone and cause progressive sensory deficits or mass effect on the brainstem. Metastatic tumors, such as from lung or breast primaries, can compress the gasserian ganglion or root entry zone, resulting in rapid-onset neuropathy with mixed sensory and motor involvement depending on the degree of infiltration.^[64]^[65] Iatrogenic trigeminal neuropathies often stem from dental procedures, particularly inferior alveolar nerve blocks targeting the mandibular division (V3), leading to persistent paresthesia or hypoesthesia. These injuries result from direct needle trauma, local anesthetic toxicity, or hematoma formation, with reported incidences ranging from approximately 1 in 14,000 to 1 in 100,000 following routine anesthetic injections, though higher rates occur in surgical contexts like implant placement.^[66]^[67]

Diagnosis and imaging

Diagnosis of trigeminal nerve disorders begins with a thorough clinical examination to assess sensory and motor functions across its three divisions. Sensory mapping involves testing light touch with a cotton wisp, pinprick with a safety pin, and temperature discrimination using warm and cold objects to identify hypoesthesia or hyperesthesia in the V1 (ophthalmic), V2 (maxillary), or V3 (mandibular) territories.^[2] The corneal reflex, elicited by touching the cornea with a wisp of cotton, evaluates the sensory (V1) and motor (facial nerve, VII) components, with absent response indicating trigeminal involvement.^[24] The jaw jerk reflex, tested by tapping the chin with the mouth slightly open, assesses the motor function of V3; an exaggerated response suggests upper motor neuron involvement, while diminution points to peripheral trigeminal dysfunction.^[2] Electrophysiological tests provide objective measures of trigeminal nerve integrity. The blink reflex, evoked by supraorbital nerve stimulation, produces an early ipsilateral R1 component reflecting V1-VII connectivity, useful for detecting proximal lesions.^[68] The masseter inhibitory reflex, recorded from masseter muscles during tooth clenching and triggered by mental nerve stimulation, evaluates V3 function and is abnormal in mandibular division disorders.^[68] Imaging modalities are essential to identify structural causes of trigeminal pathology. Magnetic resonance imaging (MRI), particularly high-resolution sequences like T2-weighted FIESTA (fast imaging employing steady-state acquisition), visualizes neurovascular compression at the root entry zone and excludes tumors or demyelination.^[69]^[70] Computed tomography (CT) is preferred for evaluating bony foramina and skull base abnormalities affecting nerve passage.^[71] Positron emission tomography (PET) can detect central pain mechanisms in refractory cases by showing metabolic changes in trigeminal pathways.^[72] Differential diagnosis distinguishes trigeminal disorders from mimics such as dental pain, migraine, or cluster headache, often requiring correlation with International Classification of Headache Disorders, third edition (ICHD-3) criteria, which specify unilateral, shock-like pain in trigeminal distribution triggered by innocuous stimuli for neuralgia.^[73]^[74] Quantitative sensory testing (QST) quantifies thresholds for thermal, mechanical, and vibratory stimuli to differentiate small-fiber (e.g., temperature, pinprick) from large-fiber (e.g., touch, vibration) involvement, aiding in characterizing neuropathic features.^[75]^[76]

Treatment and management

The treatment and management of trigeminal nerve disorders, particularly trigeminal neuralgia (TN), begin with pharmacological interventions as the first-line approach for most patients. Carbamazepine, an anticonvulsant, is recommended as the initial therapy due to its established efficacy in reducing paroxysmal pain by stabilizing neuronal membranes. Typical dosing starts at 200 mg twice daily and titrates up to 1200 mg per day, achieving initial pain relief in 70-90% of patients with classical TN. Oxcarbazepine serves as an effective alternative, particularly for those intolerant to carbamazepine, with dosing of 600-1800 mg per day and similar response rates. Other options include gabapentin (up to 3600 mg per day) and baclofen (up to 80 mg per day), which may be used as adjuncts or second-line agents, providing relief in 50-70% of refractory cases.^[77]^[78]^[79] For patients unresponsive to medications or experiencing intolerable side effects, interventional procedures offer targeted relief by disrupting pain transmission in the trigeminal pathways. Peripheral nerve blocks using lidocaine injections (1-2% solution) are commonly employed for acute exacerbations involving the maxillary (V2) or mandibular (V3) divisions, providing temporary analgesia lasting hours to days in up to 80% of applications. Glycerol rhizotomy, a percutaneous procedure involving injection of glycerol into the trigeminal cistern, yields initial pain relief in approximately 80-90% of cases, though sensory disturbances occur in 20-30% of patients.^[80]^[81]^[82] Surgical options are reserved for medically refractory TN, with microvascular decompression (MVD) considered the gold standard for classical cases caused by vascular compression. MVD involves relocating offending vessels away from the trigeminal root entry zone, achieving long-term pain freedom in 75-85% of patients at 5-10 years follow-up, with low complication rates (e.g., hearing loss in <5%). Gamma Knife radiosurgery, a noninvasive stereotactic procedure delivering focused radiation to the trigeminal root, results in 70% of patients being pain-free at 3 years, though latency to effect averages 1-3 months and recurrence occurs in 20-40%.^[83]^[84]^[85] Management of other trigeminal neuropathies varies by etiology. For postherpetic trigeminal neuropathy following herpes zoster reactivation, early antiviral therapy with acyclovir or valacyclovir (within 72 hours of rash onset) reduces acute pain and prevents progression to chronic neuralgia in 50-70% of cases. Autoimmune-mediated neuropathies, such as those associated with multiple sclerosis or sarcoidosis, may require immunosuppressants like corticosteroids or rituximab, which stabilize symptoms in 60-80% of responsive patients. General neuropathic pain control in these conditions often incorporates tricyclic antidepressants (e.g., amitriptyline 25-150 mg/day) or serotonin-norepinephrine reuptake inhibitors (e.g., duloxetine 60-120 mg/day), yielding moderate relief in 40-60%.^[54]^[69] A multidisciplinary approach enhances outcomes for chronic trigeminal pain, integrating neuromodulation techniques such as transcutaneous electrical nerve stimulation (TENS), which provides adjunctive relief in 30-50% of patients by modulating sensory input. Cognitive-behavioral therapy (CBT) addresses the psychological burden of persistent pain, improving coping and reducing healthcare utilization in 40-60% of chronic cases. Long-term follow-up is essential, as recurrence rates range from 20-30% across interventions, necessitating vigilant monitoring and potential retreatment.^[86]^[87]^[88]

References

[1]
Neuroanatomy, Cranial Nerve 5 (Trigeminal) - StatPearls - NCBI - NIH
Apr 20, 2024 · The trigeminal nerve is the largest cranial nerve, providing facial sensory innervation and motor impulses to the mastication muscles.Introduction · Structure and Function · Embryology · Blood Supply and Lymphatics
[2]
Cranial Nerve V: The Trigeminal Nerve - Clinical Methods - NCBI - NIH
The sensory portion of the trigeminal supplies touch–pain–temperature to the face. The nerve has three divisions: the ophthalmic, maxillary, and mandibular ...
[3]
The Superior Cerebellar Artery: Variability and Clinical Significance
Jul 17, 2023 · The superior cerebellar artery (SCA) arises from the distal part of the basilar artery and passes by the oculomotor, trochlear, and trigeminal nerves.
[4]
Trigeminal Cave - an overview | ScienceDirect Topics
Trigeminal Cave, also known as Meckel's Cave, is a cerebrospinal fluid ... the dura mater: trigeminal cave, which is a doubling of the tentorium cerebelli.
[5]
Trigeminal Nerve: What It Is, Anatomy, Function & Conditions
It's located within Meckel's cave, a space filled with cerebrospinal fluid between two layers of dura mater over your temporal bone. The trigeminal ganglion ...Overview · Function · Conditions And DisordersMissing: composition neurons protective
[6]
Neuroanatomy, Semilunar Ganglion - StatPearls - NCBI Bookshelf
Mar 20, 2023 · The semilunar sensory ganglion (also known as the trigeminal ganglion or Gasserian ganglion) is a thin, crescent-shaped structure in the ...Missing: 30000-50000 | Show results with:30000-50000
[7]
Numbers of neurons and non-neuronal cells in human trigeminal ...
Neuronal counts in each of the 16 ganglia ranged from 20,000 to 35,400, with an average of 27,400 +/- 4800, and the estimated ratio of non-neuronal to neuronal ...
[8]
The Trigeminal Nerve (CN V) - Course - Divisions - TeachMeAnatomy
The trigeminal ganglion is located lateral to the cavernous sinus, in a depression of the temporal bone. This depression is known as the trigeminal cave. The ...Anatomical Course · Divisions · Mandibular NerveMissing: composition protective
[9]
Trigeminal Nerve Anatomy - Medscape Reference
Feb 20, 2025 · In the trigeminal ganglion, CGRP is produced in sensory C- and Aδ-fibers, which project to various parts of the face, head, and intracranial ...Gross Anatomy · Connections · Related Clinical Conditions...Missing: composition protective layers<|control11|><|separator|>
[10]
Robot-assisted trigeminal nerve rhizotomy with radiofrequency ... - NIH
Jun 16, 2025 · The primary goal of trigeminal rhizotomy is to disrupt the nerve's ability to transmit pain signals by targeting the gasserian ganglion, located ...
[11]
Cranial Nerve Anatomy/Cranial Nerves
May 3, 2017 · V1 - Ophthalmic Nerve · Communicating branch to ciliary ganglion · Long Ciliary Nerve - provides sensation to cornea/sclera, carries sympathetic ...
[12]
Anatomy, Head and Neck, Maxillary Nerve - StatPearls - NCBI - NIH
Jun 5, 2023 · The fifth cranial nerve, known as the trigeminal nerve (V), is the largest of the twelve cranial nerves and carries both sensory and motor ...Introduction · Structure and Function · Nerves · Physiologic Variants<|control11|><|separator|>
[13]
Anatomy, Head and Neck, Mandibular Nerve - StatPearls - NCBI - NIH
The motor root runs along the trigeminal cave and joins the sensory root before leaving the skull through the foramen ovale and enters the infratemporal fossa.
[14]
Nerves of the Head and Neck | UAMS Department of Neuroscience
internal carotid n. superior cervical sympathetic ganglion, contributes to the internal carotid plexus, vascular smooth muscle of the external carotid system of ...<|control11|><|separator|>
[15]
Anatomy Tables - Infratemporal Fossa & Oral Cavity
trigeminal ganglion; motor root of trigeminal from pons, meningeal br., medial & lateral pterygoid, masseteric, anterior & posterior deep temporal, buccal ...
[16]
Dermatomes: What They Are & Locations - Cleveland Clinic
Oct 27, 2022 · C2 to C3: Upper neck, a small area of your jaw underneath each ear and back of your head; C3 to C4: Lower neck, upper chest and upper back.Missing: trigeminal | Show results with:trigeminal
[17]
Corneal Innervation and Sensation: The Eye and Beyond - PMC
Mar 28, 2018 · With a central corneal nerve density of approximately 7,000 nociceptors per square millimeter [4,7], the cornea is 300 to 600 times more ...
[18]
Facial pain – A diagnostic challenge - RACGP
Acute maxillary sinusitis may present as pain in the region of the upper molar teeth, which may also be tender to percussion. Chronic sinusitis can result from ...Facial Pain · Maxillary Sinusitis · Trigeminal Neuralgia
[19]
Anatomy, Head and Neck, Mastication Muscles - StatPearls - NCBI
The nerve supply to these muscles begins by the eighth week. ... The mandibular nerve is the only division of the trigeminal nerve that carries motor fibers.
[20]
Evaluation of Bite Force After Open Reduction and Internal Fixation ...
The range varies from 334–421 Newtons, 323–398 Newtons, and 168–208 Newtons for right molars, left molars, and incisors, respectively.
[21]
Cranial Nerve Testing - StatPearls - NCBI Bookshelf - NIH
Trigeminal neuralgia presents as neuropathic, shock-like facial pain within the trigeminal dermatomal distribution (V2 and V3 divisions).[51] This neuralgia ...
[22]
Neuroanatomy, Trigeminal Reflexes - StatPearls - NCBI Bookshelf
The trigeminal nerve is responsible for the primary sensory input from the head and neck as well as providing motor innervation to the muscles of mastication.
[23]
Corneal Reflex - StatPearls - NCBI Bookshelf
The corneal blink reflex is caused by a loop between the trigeminal sensory nerves and the facial motor (VII) nerve innervation of the orbicularis oculi muscles ...Definition/Introduction · Issues of Concern · Clinical Significance
[24]
localisation of the human sneezing centre? - PMC - PubMed Central
Sneezing abnormalities are usually caused by irritation of the trigeminal nerve terminals in the nasal mucosa. In the last few years, some clinical reports ...
[25]
Physiology, Gag Reflex - StatPearls - NCBI Bookshelf
Mar 12, 2023 · Stimulation of the soft palate can also elicit the gag reflex; in this case, the sensory limb is the trigeminal nerve (CN V). Here, sensory ...
[26]
Neuroanatomy, Trigeminal Nucleus - StatPearls - NCBI Bookshelf
May 1, 2023 · The trigeminal nerve (cranial nerve V; CN V) is a mixed sensory and motor nerve. It supplies the face via three branches of the nerve: from ...
[27]
Trigeminal Neuropathy - StatPearls - NCBI Bookshelf - NIH
Mar 1, 2024 · Trigeminal neuropathy refers to dysfunction in sensory or motor functions involving cranial nerve V, the trigeminal nerve.
[28]
Main sensory nucleus of the trigeminal nerve - Radiopaedia.org
Jun 27, 2024 · The dorsomedial division receives afferent input from the oral cavity. The ventrolateral division receives input from all three divisions (V1-V3) ...
[29]
Principal Sensory Trigeminal Nucleus - ScienceDirect.com
The principal sensory trigeminal nucleus is defined as a structure in the pons that receives nociceptive fibers from the tooth pulp and oral cavity, playing a ...
[30]
Neuroanatomy, Spinal Trigeminal Nucleus - StatPearls - NCBI - NIH
The spinal trigeminal nucleus (SN) is a sensory tract located in the lateral medulla of the brain stem whose principal function is relaying pain and ...
[31]
New Insights in Trigeminal Anatomy: A Double Orofacial Tract for Nociceptive Input - PMC
Summary of each segment:
[32]
Cerebellar afferences from the mesencephalic trigeminal nucleus in ...
The aim of the present study was to test for and characterize the organization of a direct projection from neurones of the trigeminal mesencephalic nucleus ...
[33]
Somatosensory Pathways (Section 2, Chapter 4) Neuroscience Online
The neurotransmitter is released onto 2° afferents within the main sensory trigeminal nucleus. The 2° afferent generates action potentials that are conducted ...
[34]
Trigeminal neuralgia: An overview from pathophysiology to ...
The trigeminal nerve (V) is the fifth and largest of all cranial nerves, and it is responsible for detecting sensory stimuli that arise from the craniofacial ...
[35]
Birth of ophthalmic trigeminal neurons initiates early in the placodal ...
The trigeminal ganglion owes its embryonic origin to two different cell populations—trigeminal placode and neural crest. Whilst placode cells uniquely form ...
[36]
The development of the neural crest in the human - PMC - NIH
Short nerve fibres appear in the trigeminal ganglion at stage 12. The trigeminal ganglion receives some contributions from the ectoderm (Fig. 4C), and this was ...
[37]
Embryonic stages in cerebellar afferent development - PMC
The motor component is derived from the basal plate of the embryonic pons, while the sensory component originates from the alar plate and the neural crest ...
[38]
Neural crest and placode interaction during the development of the ...
Here we review the evidence that neural crest and placode cells remain in close proximity throughout their development and interact repeatedly in a reciprocal ...
[39]
A three‐dimensional analysis of the development of cranial nerves ...
The intricate branching of the right trigeminal nerve in a human embryo. A 3D reconstruction of the CN V is provided in CS 23 specimen #950 (56–60 days of ...<|control11|><|separator|>
[40]
The Neural Crest - Developmental Biology - NCBI Bookshelf
The neural crest cells originating in the forebrain and midbrain contribute to the frontonasal process, palate, and mesenchyme of the first pharyngeal arch.
[41]
Analysis of early human neural crest development - PMC
Depending on their origin, cranial NCCs will either migrate through the facial mesenchyme and into the frontonasal process, or will populate the branchial ...
[42]
Pax3-expressing trigeminal placode cells can localize to ... - PubMed
Sep 15, 2002 · Pax3 is the earliest known marker of opV placode ectoderm in the chick. Pax3 is also expressed transiently by neural crest cells as they ...
[43]
Making a head: Neural crest and ectodermal placodes in cranial ...
Here, we review the origins of both neural crest and placode cells at the neural plate border of the early vertebrate embryo and investigate the molecular and ...
[44]
Influence of mesodermal Fgf8 on the differentiation of neural crest ...
Our findings support the view that global expression of Fgf8 is required for early NC survival and differentiation of placode-derived sensory neurons, and ...
[45]
Isolated aglossia congenita: A rare case of oromandibular limb ... - NIH
Aglossia congenita (AC), congenital absence of the tongue, is a rare and unusual midline developmental anomaly usually associated with craniofacial and limb ...
[46]
Distribution Of The Mylohyoid Nerve: Anatomical Variability And ...
Aug 10, 2025 · The mylohyoid nerve is a branch of the mandibular division of the trigeminal nerve that provides motor supply to the mylohyoid and digastric ...
[47]
Persistent trigeminal artery linked with partial duplication of the ... - NIH
Jul 16, 2025 · The persistent trigeminal artery (PTA) is the most common persistent vessel, with an estimated pooled prevalence of 0.3% [2]. Nevertheless, the ...
[48]
Trigeminal Nerve Compression Without Trigeminal Neuralgia - NIH
Feb 6, 2018 · Cadaveric observations have demonstrated vascular compression of the trigeminal nerve in 13% to 58% of individuals without TN as compared to ...
[49]
MRI of the Trigeminal Nerve in Patients With Trigeminal Neuralgia ...
Feb 22, 2016 · View through operative microscope shows trigeminal nerve (arrow) being compressed by superior cerebellar artery (arrowhead) along its rostral ...
[50]
Trigeminal Neuralgia - StatPearls - NCBI Bookshelf - NIH
Mar 3, 2024 · The trigeminal nerve has 3 divisions: ophthalmic (V1), maxillary (V2), and mandibular (V3). The anatomical areas innervated by each division ...Missing: dermatomes | Show results with:dermatomes
[51]
Trigeminal Neuralgia: Basic and Clinical Aspects - PMC
It has three branches that provide the main sensory innervation of the anterior two-thirds of the head and face. Trigeminal neuralgia (TN) is characterized by ...
[52]
Trigeminal neuralgia: a practical guide - PMC - PubMed Central
Jun 9, 2021 · Trigeminal neuralgia (TN) is a highly disabling disorder characterised by very severe, brief and electric shock like recurrent episodes of facial pain.
[53]
Acute Herpes Zoster and Postherpetic Neuralgia
The incidence of developing PHN is 10-25%,1 and increases with age, more severe rash and acute HZ pain, ophthalmic involvement, and presence of prodromal ...
[54]
Radiofrequency regulation of the sphenopalatine ganglion in ...
Apr 19, 2024 · Studies have indicated that 20% of all patients with herpes zoster have occurrences in the trigeminal ganglion, with the incidence in the first ...
[55]
Post-herpetic trigeminal neuralgia treated with deep brain stimulation
Post-herpetic neuralgic affects up to 20% of patients after an attack of trigeminal Herpes Zoster infection. Past medical and surgical treatments have been ...
[56]
Cranial Neuropathy As Initial Manifestation of Primary Sjögren's ...
Jan 27, 2024 · The pathophysiology of trigeminal sensory neuropathy is unclear. It may be related to myelin sheath loss, axonal degeneration, or vasculitis. It ...
[57]
Isolated Bilateral Trigeminal Neuropathy in Sarcoidosis Presenting ...
The trigeminal neuropathy was thought to be secondary to sarcoidosis after all other causes of trigeminal nerve involvement were ruled out.
[58]
Lateral Medullary Syndrome (Wallenberg Syndrome) - StatPearls
Aug 9, 2025 · Lateral medullary syndrome (LMS), also known as Wallenberg syndrome, is a neurological disorder affecting the dorsolateral medulla oblongata ...
[59]
Central trigeminal involvement in multiple sclerosis using high ...
Both facial pain (including trigeminal neuralgia) and non-painful facial sensory disturbance are routinely encountered in patients with multiple sclerosis (MS).
[60]
Trigeminal Schwannomas | Clinical Gate
Mar 26, 2015 · Trigeminal schwannomas (TSs) are benign, slow-growing tumors arising from the peripheral nerve sheath of the trigeminal nerve.
[61]
Isolated Trigeminal Nerve Metastases from Breast Cancer
The metastatic pathways through which malignant tumors can involve the trigeminal nerve or ganglion ... compression of the trigeminal nerve root, near to ...
[62]
Neuropathy of Trigeminal Nerve Branches After Oral and ...
This study shows a low incidence of nerve damage among the new patients presenting in oral and maxillofacial surgery clinic (<1 %);Missing: V3 | Show results with:V3
[63]
Trigeminal neuropathies following dental anesthetic blocks: a review ...
Estimates range between 0.5% and 5% among individuals undergoing oral and maxillofacial procedures (5-7), but the exact figures may vary according to the ...
[64]
Electrophysiological evidence of subclinical trigeminal dysfunction ...
Oct 14, 2022 · Electrophysiological evaluation of the masseter inhibitory reflex (MIR) and blink reflex (BR) was carried out to test the functional integrity ...
[65]
Trigeminal neuralgia - Diagnosis and treatment - Mayo Clinic
Dec 28, 2023 · In a rhizotomy, your surgeon destroys nerve fibers to reduce pain. This causes some facial numbness. Types of rhizotomy include: Glycerol ...
[66]
Central nervous system lymphoma presenting as trigeminal neuralgia
Axial fast imaging employing steady state acquisition (FIESTA) sequence MRI demonstrates the anatomy of the cranial nerves in relation to the mass lesion.
[67]
Imaging evaluation of trigeminal neuralgia - PMC - PubMed Central
MRI is helpful to confirm neurovascular contact when present and to exclude other causes, which may occur anywhere from the brainstem to the extracranial space.Anatomy Of The Fifth Cranial... · Brainstem · Cisternal Space And Meckel's...Missing: disorders | Show results with:disorders
[68]
Image findings of cranial nerve pathology on [18F]-2 - NIH
Dec 3, 2015 · This article aims to increase awareness about the utility of 18 F -FDG-PET/CT in the evaluation of cranial nerve (CN) pathology.
[69]
Trigeminal neuralgia: New classification and diagnostic grading for ...
Diffusion tensor imaging (DTI) and fiber tractography detect abnormalities of the trigeminal nerve root that normalize following decompression or radiosurgery. ...
[70]
Orofacial Migraine and Other Idiopathic Non-Dental Facial Pain ...
Oct 20, 2023 · Trigeminal neuralgia is more represented, followed by cluster headaches and migraines.
[71]
Analysis of trigeminal nerve disorders after oral and maxillofacial ...
Oct 26, 2010 · Quantitative sensory testing (QST) is a reliable, non-invasive psychophysical test of large- and small-fiber sensory modalities [16], which has ...
[72]
The Role of Quantitative Sensory Testing in the Evaluation of ...
Quantitative sensory testing (QST) is a noninvasive method of assessing sensory and pain perception that has been used in the past 30 years primarily for ...
[73]
The diagnostic evaluation and treatment of trigeminal neuralgia (an ...
The diagnosis of symptomatic TN (STN) is made when investigations identify a structural abnormality other than potential vascular compression affecting the ...Abstract · Analysis Of Evidence · Gamma Knife Surgery
[74]
Update on neuropathic pain treatment for trigeminal neuralgia
These guidelines recommend carbamazepine (200-1200 mg/d) and oxcarbazepine (600-1800 mg/d) as a first-line therapy for classic TN. Carbamazepine. Carbamazepine ...
[75]
European Academy of Neurology guideline on trigeminal neuralgia
For long-term treatment, carbamazepine or oxcarbazepine are recommended as drugs of first choice. Lamotrigine, gabapentin, botulinum toxin type A, pregabalin, ...
[76]
A systematic review of rescue analgesic strategies in acute ...
Current recommendations include the use of topical, injected or iv lidocaine, iv fosphenytoin, and topical or injected sumatriptan to abort an acute attack.
[77]
Percutaneous glycerol rhizotomy for trigeminal neuralgia - PubMed
There was an overall success rate of 92.1% in improvement of facial pain. Nine patients had reduced facial sensation post-operatively. There were no cases of ...
[78]
Percutaneous Balloon Compression vs ... - Neurosurgery
For PRGR, with technical failures excluded, the initial success rate was 85%, and the median pain-free time was 21 months, with 47 patients (38%) free of pain ...
[79]
The Long-Term Outcome of Microvascular Decompression for ...
Apr 25, 1996 · Fujimaki et al. reported that 28 percent of patients were free of pain 54 months after glycerol rhizotomy; Burchiel reported similar results.<|separator|>
[80]
Long-term outcome of microvascular decompression for typical ...
Apr 12, 2024 · From a meta-analysis of 4884 MVDs, the average acute pain-free rate was 91%, and the average follow-up pain-free and recurrence rates were 76.6% ...
[81]
Gamma knife surgery for trigeminal neuralgia: outcomes and ...
Some degree of pain improvement at 3 years post-GKS was noted in 70% of patients with TN. Although less effective than MVD, GKS remains a reasonable treatment ...
[82]
Guidelines for the management of trigeminal neuralgia - PubMed
Jun 1, 2023 · Guidelines for the diagnosis and treatment of patients with trigeminal neuralgia (TN) advocate for a multidisciplinary team approach to improve the care of ...
[83]
[PDF] TRIGEMINAL NEURALGIA - American Academy of Neurology
This is a summary of the American Academy of Neurology (AAN) guideline regarding recommended use and best practices for diagnosis and treatment of patients with ...
[84]
Repeat microvascular decompression for patients with persistent
The complete pain relief rates of repeat MVD were 87.8% immediately after surgery and 75% at last follow-up. Thirteen patients (31.7%) had new or increased ...