Insertions of the Lateral Pterygoid Muscle to the Disc-Capsule Complex of the Temporomandibular Joint and Condyle
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The Myloglossus in a Human Cadaver Study: Common Or Uncommon Anatomical Structure? B
Folia Morphol. Vol. 76, No. 1, pp. 74–81 DOI: 10.5603/FM.a2016.0044 O R I G I N A L A R T I C L E Copyright © 2017 Via Medica ISSN 0015–5659 www.fm.viamedica.pl The myloglossus in a human cadaver study: common or uncommon anatomical structure? B. Buffoli*, M. Ferrari*, F. Belotti, D. Lancini, M.A. Cocchi, M. Labanca, M. Tschabitscher, R. Rezzani, L.F. Rodella Section of Anatomy and Physiopathology, Department of Clinical and Experimental Sciences, University of Brescia, Brescia, Italy [Received: 1 June 2016; Accepted: 18 July 2016] Background: Additional extrinsic muscles of the tongue are reported in literature and one of them is the myloglossus muscle (MGM). Since MGM is nowadays considered as anatomical variant, the aim of this study is to clarify some open questions by evaluating and describing the myloglossal anatomy (including both MGM and its ligamentous counterpart) during human cadaver dissections. Materials and methods: Twenty-one regions (including masticator space, sublin- gual space and adjacent areas) were dissected and the presence and appearance of myloglossus were considered, together with its proximal and distal insertions, vascularisation and innervation. Results: The myloglossus was present in 61.9% of cases with muscular, ligamen- tous or mixed appearance and either bony or muscular insertion. Facial artery pro- vided myloglossal vascularisation in the 84.62% and lingual artery in the 15.38%; innervation was granted by the trigeminal system (buccal nerve and mylohyoid nerve), sometimes (46.15%) with hypoglossal component. Conclusions: These data suggest us to not consider myloglossus as a rare ana- tomical variant. -
MRI-Based Assessment of Masticatory Muscle Changes in TMD Patients After Whiplash Injury
Journal of Clinical Medicine Article MRI-Based Assessment of Masticatory Muscle Changes in TMD Patients after Whiplash Injury Yeon-Hee Lee 1,* , Kyung Mi Lee 2 and Q-Schick Auh 1 1 Department of Orofacial Pain and Oral Medicine, Kyung Hee University Dental Hospital, #613 Hoegi-dong, Dongdaemun-gu, Seoul 02447, Korea; [email protected] 2 Department of Radiology, Kyung Hee University College of Medicine, Kyung Hee University Hospital, #26 Kyunghee-daero, Dongdaemun-gu, Seoul 02447, Korea; [email protected] * Correspondence: [email protected]; Tel.: +82-2-958-9409; Fax: +82-2-968-0588 Abstract: Objective: to investigate the change in volume and signal in the masticatory muscles and temporomandibular joint (TMJ) of patients with temporomandibular disorder (TMD) after whiplash injury, based on magnetic resonance imaging (MRI), and to correlate them with other clinical parameters. Methods: ninety patients (64 women, 26 men; mean age: 39.36 ± 15.40 years), including 45 patients with symptoms of TMD after whiplash injury (wTMD), and 45 age- and sex- matched controls with TMD due to idiopathic causes (iTMD) were included. TMD was diagnosed using the study diagnostic criteria for TMD Axis I, and MRI findings of the TMJ and masticatory muscles were investigated. To evaluate the severity of TMD pain and muscle tenderness, we used a visual analog scale (VAS), palpation index (PI), and neck PI. Results: TMD indexes, including VAS, PI, and neck PI were significantly higher in the wTMD group. In the wTMD group, muscle tenderness was highest in the masseter muscle (71.1%), and muscle tenderness in the temporalis (60.0%), lateral pterygoid muscle (LPM) (22.2%), and medial pterygoid muscle (15.6%) was significantly more frequent than that in the iTMD group (all p < 0.05). -
The Mandibular Nerve - Vc Or VIII by Prof
The Mandibular Nerve - Vc or VIII by Prof. Dr. Imran Qureshi The Mandibular nerve is the third and largest division of the trigeminal nerve. It is a mixed nerve. Its sensory root emerges from the posterior region of the semilunar ganglion and is joined by the motor root of the trigeminal nerve. These two nerve bundles leave the cranial cavity through the foramen ovale and unite immediately to form the trunk of the mixed mandibular nerve that passes into the infratemporal fossa. Here, it runs anterior to the middle meningeal artery and is sandwiched between the superior head of the lateral pterygoid and tensor veli palatini muscles. After a short course during which a meningeal branch to the dura mater, and the nerve to part of the medial pterygoid muscle (and the tensor tympani and tensor veli palatini muscles) are given off, the mandibular trunk divides into a smaller anterior and a larger posterior division. The anterior division receives most of the fibres from the motor root and distributes them to the other muscles of mastication i.e. the lateral pterygoid, medial pterygoid, temporalis and masseter muscles. The nerve to masseter and two deep temporal nerves (anterior and posterior) pass laterally above the medial pterygoid. The nerve to the masseter continues outward through the mandibular notch, while the deep temporal nerves turn upward deep to temporalis for its supply. The sensory fibres that it receives are distributed as the buccal nerve. The 1 | P a g e buccal nerve passes between the medial and lateral pterygoids and passes downward and forward to emerge from under cover of the masseter with the buccal artery. -
New Knowledge Resource for Anatomy Enables Comprehensive Searches of the Literature on the Feeding Muscles of Mammals
RESEARCH ARTICLE Muscle Logic: New Knowledge Resource for Anatomy Enables Comprehensive Searches of the Literature on the Feeding Muscles of Mammals Robert E. Druzinsky1*, James P. Balhoff2, Alfred W. Crompton3, James Done4, Rebecca Z. German5, Melissa A. Haendel6, Anthony Herrel7, Susan W. Herring8, Hilmar Lapp9,10, Paula M. Mabee11, Hans-Michael Muller4, Christopher J. Mungall12, Paul W. Sternberg4,13, a11111 Kimberly Van Auken4, Christopher J. Vinyard5, Susan H. Williams14, Christine E. Wall15 1 Department of Oral Biology, University of Illinois at Chicago, Chicago, Illinois, United States of America, 2 RTI International, Research Triangle Park, North Carolina, United States of America, 3 Organismic and Evolutionary Biology, Harvard University, Cambridge, Massachusetts, United States of America, 4 Division of Biology and Biological Engineering, M/C 156–29, California Institute of Technology, Pasadena, California, United States of America, 5 Department of Anatomy and Neurobiology, Northeast Ohio Medical University, Rootstown, Ohio, United States of America, 6 Oregon Health and Science University, Portland, Oregon, ’ OPEN ACCESS United States of America, 7 Département d Ecologie et de Gestion de la Biodiversité, Museum National d’Histoire Naturelle, Paris, France, 8 University of Washington, Department of Orthodontics, Seattle, Citation: Druzinsky RE, Balhoff JP, Crompton AW, Washington, United States of America, 9 National Evolutionary Synthesis Center, Durham, North Carolina, Done J, German RZ, Haendel MA, et al. (2016) United States of America, 10 Center for Genomic and Computational Biology, Duke University, Durham, Muscle Logic: New Knowledge Resource for North Carolina, United States of America, 11 Department of Biology, University of South Dakota, Vermillion, South Dakota, United States of America, 12 Genomics Division, Lawrence Berkeley National Laboratory, Anatomy Enables Comprehensive Searches of the Berkeley, California, United States of America, 13 Howard Hughes Medical Institute, M/C 156–29, California Literature on the Feeding Muscles of Mammals. -
Appendix B: Muscles of the Speech Production Mechanism
Appendix B: Muscles of the Speech Production Mechanism I. MUSCLES OF RESPIRATION A. MUSCLES OF INHALATION (muscles that enlarge the thoracic cavity) 1. Diaphragm Attachments: The diaphragm originates in a number of places: the lower tip of the sternum; the first 3 or 4 lumbar vertebrae and the lower borders and inner surfaces of the cartilages of ribs 7 - 12. All fibers insert into a central tendon (aponeurosis of the diaphragm). Function: Contraction of the diaphragm draws the central tendon down and forward, which enlarges the thoracic cavity vertically. It can also elevate to some extent the lower ribs. The diaphragm separates the thoracic and the abdominal cavities. 2. External Intercostals Attachments: The external intercostals run from the lip on the lower border of each rib inferiorly and medially to the upper border of the rib immediately below. Function: These muscles may have several functions. They serve to strengthen the thoracic wall so that it doesn't bulge between the ribs. They provide a checking action to counteract relaxation pressure. Because of the direction of attachment of their fibers, the external intercostals can raise the thoracic cage for inhalation. 3. Pectoralis Major Attachments: This muscle attaches on the anterior surface of the medial half of the clavicle, the sternum and costal cartilages 1-6 or 7. All fibers come together and insert at the greater tubercle of the humerus. Function: Pectoralis major is primarily an abductor of the arm. It can, however, serve as a supplemental (or compensatory) muscle of inhalation, raising the rib cage and sternum. (In other words, breathing by raising and lowering the arms!) It is mentioned here chiefly because it is encountered in the dissection. -
The Independent Functions of the Two Heads of the Lateral Pterygoid Muscle
The Independent Functions of the Two Heads of the Lateral Pterygoid Muscle JAMES A. McNAMARA, JR. Department of Anatomy and Center for Human Growth and Development, The University of Michigan, Ann Arbor, Michigan 48104 ABSTRACT Investigations on the role of the lateral pterygoid muscle in mandibular movements have been limited due to difficulties in obtaining con- sistent neuromuscular recordings in human subjects. The rhesus monkey was used as a substitute experimental animal. Thirty-three Macaca mulatta were monitored in 113 electromyographic recording sessions. Two distinct functional patterns were identified from the region of the lateral pterygoid muscle, depend- ing upon the location of the electrodes within this muscle. Through anatomical dissection of areas of electrode placement in 12 animals, the two patterns of activity were related to the inferior and superior heads of the lateral pterygoid muscle. The inferior head acted synergistically with the suprahyoid muscle group in opening movements of the mandible. No activity was noted in closing movements, or in swallowing. In contrast, the superior head was not active dur- ing opening movements. Electromyographic activity of the superior head, an- tagonistic to the suprahyoid muscles, was observed during such closing move- ments as chewing and clenching of the teeth and during deglutition. The superior head presumably positioned or stabilized the condylar head and disc against the articular eminence during closing movements of the mandible, while the in- ferior head assisted in the translation of the condylar head downward, anteriorly, and contralaterally during opening movements. Thus, the two heads of the lateral pterygoid can be considered as two functionally distinct muscles. -
The Mandibular Nerve: the Anatomy of Nerve Injury and Entrapment
5 The Mandibular Nerve: The Anatomy of Nerve Injury and Entrapment M. Piagkou1, T. Demesticha2, G. Piagkos3, Chrysanthou Ioannis4, P. Skandalakis5 and E.O. Johnson6 1,3,4,5,6Department of Anatomy, 2Department of Anesthesiology, Metropolitan Hospital Medical School, University of Athens Greece 1. Introduction The trigeminal nerve (TN) is a mixed cranial nerve that consists primarily of sensory neurons. It exists the brain on the lateral surface of the pons, entering the trigeminal ganglion (TGG) after a few millimeters, followed by an extensive series of divisions. Of the three major branches that emerge from the TGG, the mandibular nerve (MN) comprises the 3rd and largest of the three divisions. The MN also has an additional motor component, which may run in a separate facial compartment. Thus, unlike the other two TN divisions, which convey afferent fibers, the MN also contains motor or efferent fibers to innervate the muscles that are attached to mandible (muscles of mastication, the mylohyoid, the anterior belly of the digastric muscle, the tensor veli palatini, and tensor tympani muscle). Most of these fibers travel directly to their target tissues. Sensory axons innervate skin on the lateral side of the head, tongue, and mucosal wall of the oral cavity. Some sensory axons enter the mandible to innervate the teeth and emerge from the mental foramen to innervate the skin of the lower jaw. An entrapment neuropathy is a nerve lesion caused by pressure or mechanical irritation from some anatomic structures next to the nerve. This occurs frequently where the nerve passes through a fibro-osseous canal, or because of impingement by an anatomic structure (bone, muscle or a fibrous band), or because of the combined influences on the nerve entrapment between soft and hard tissues. -
Submandibular Region
20/02/2013 Learning Outcomes • The Mandible • The Submandibular – Surface Anatomy Region – Muscle Attachments – Submandibular Gland Submandibular Region • The Floor of the Mouth – Sublingual Gland (FOM) – Lingual Nerve – Muscles of the FOM • The Head & Neck Mohammed A Al-Muharraqi MBChB, BDS, MSc, MRCS Glas, FFD RCS Irel, MFDS RCS Eng • The Tongue Parasympathetics – Muscles of the Tongue e-mail: [email protected] Mandible Mandible Head of Condylar Process Coronoid Process Neck of Pterygoid Fovea Neck of Condylar Condylar Process Condylar Process Ramus of Mandible Process Condylar Process Anterior Border of Ramus Lingula Coronoid Process Mandibular Coronoid Lingual (Genial) Foramen (Mandibular) Foramen Notch Alveolar Ridge Mylohyoid Line Oblique Line Alveolar Ridge Posterior Border of Ramus of Mandible Ramus Angle of Mandible Incisive Fossa Mylohyoid Groove Angle of Mandible Symphysis Menti (Median Ridge) Inferior Border of Submandibular Fossa Body of Mandible Body Mental Protuberance Sublingual Fossa Digastric Fossa Mental Foramen Superior Mental Spine Inferior Mental Spine Mental Tubercle (Genial Tubercle) (Genial Tubercle) Inferior Border of Body Muscle Attachments The mental tubercle (a raised prominence at Mandible Ligaments the mental symphysis) is a point of muscular attachment. The external surface of the ramus is covered by the attachment of the masseter muscle. On the inner surface of the body of the mandible, there is a horizontal mylohyoid line, which attaches the mylohyoid muscle. Above it, there is a shallow depression for the sublingual salivary gland and below it a deeper depression for the submandibular gland. At the anterior ends of the mylohyoid lines and superior to them, near the symphysis, there is the genial tubercles. -
Head and Neck of the Mandible
Relationships The parotid duct passes lateral (superficial) and anterior to the masseter muscle. The parotid gland is positioned posterior and lateral (superficial) to the masseter muscle. The branches of the facial nerve pass lateral (superficial) to the masseter muscle. The facial artery passes lateral (superficial) to the mandible (body). On the face, the facial vein is positioned posterior to the facial artery. The sternocleidomastoid muscle is positioned superficial to both the omohyoid muscle and the carotid sheath. The external jugular vein passes lateral (superficial) to the sternocleidomastoid muscle. The great auricular and transverse cervical nerves pass posterior and lateral (superficial) to the sternocleidomastoid muscle. The lesser occipital nerve passes posterior to the sternocleidomastoid muscle. The accessory nerve passes medial (deep) and then posterior to the sternocleidomastoid muscle. The hyoid bone is positioned superior to the thyroid cartilage. The omohyoid muscle is positioned anterior-lateral to the sternothyroid muscle and passes superficial to the carotid sheath. At the level of the thyroid cartilage, the sternothyroid muscle is positioned deep and lateral to the sternohyoid muscle. The submandibular gland is positioned posterior and inferior to the mylohyoid muscle. The digastric muscle (anterior belly) is positioned superficial (inferior-lateral) to the mylohyoid muscle. The thyroid cartilage is positioned superior to the cricoid cartilage. The thyroid gland (isthmus) is positioned directly anterior to the trachea. The thyroid gland (lobes) is positioned directly lateral to the trachea. The ansa cervicalis (inferior root) is positioned lateral (superficial) to the internal jugular vein. The ansa cervicalis (superior root) is positioned anterior to the internal jugular vein. The vagus nerve is positioned posterior-medial to the internal jugular vein and posterior-lateral to the common carotid artery. -
Botulinum Toxin Injection
Toxins 2015, 7, 2791-2800; doi:10.3390/toxins7082791 OPEN ACCESS toxins ISSN 2072-6651 www.mdpi.com/journal/toxins Review Temporomandibular Myofacial Pain Treated with Botulinum Toxin Injection Niv Mor 1,2,*, Christropher Tang 1,2 and Andrew Blitzer 1,2 1 Mount Sinai Roosevelt Hospital, Department of Otolaryngology—Head and Neck Surgery, New York, NY 10019, USA; E-Mails: [email protected] (C.T.); [email protected] (A.B.) 2 Head and Neck Surgical Group—New York Center for Voice and Swallowing Disorders, New York, NY 10019, USA * Author to whom correspondence should be addressed; E-Mail: [email protected]; Tel.: +1-212-262-4444; Fax: +1-212-523-6364. Academic Editor: Holger Barth Received: 14 June 2015 / Accepted: 13 July 2015 / Published: 24 July 2015 Abstract: This article reviews the diagnoses and treatment of temporomandibular disorders (TMD) and outlines of the role of botulinum toxin (BoNT) in the treatment of myofacial TMD. This manuscript includes a brief history of the use of BoNT in the treatment of pain, the mechanism of action of BoNT, and the techniques for injections, adverse effects and contraindications when using BoNT to treat mayofacial pain caused by TMD. Keywords: temporomandibular joint; temporomandibular disorders; botulinum toxin; myofacial pain 1. Introduction The temporomandibular joint (TMJ) is a hinged synovial joint that connects the mandible to the temporal bone at the skull base, and the posterior boarder of the TMJ is the anterior boarder of the external auditory canal. The TMJ is one of the few synovial joints with an articular disc and it functions as both a hinge joint and a sliding joint. -
Temporomandibular Joint (TMJ)
Regions of the Head 9. Oral Cavity & Perioral Regions Temporomandibular Joint (TMJ) Zygomatic process of temporal bone Articular tubercle Mandibular Petrotympanic fossa of TMJ fissure Postglenoid tubercle Styloid process External acoustic meatus Mastoid process (auditory canal) Atlanto- occipital joint Fig. 9.27 Mandibular fossa of the TMJ tubercle. Unlike other articular surfaces, the mandibular fossa is cov- Inferior view of skull base. The head (condyle) of the mandible artic- ered by fi brocartilage, not hyaline cartilage. As a result, it is not as ulates with the mandibular fossa of the temporal bone via an articu- clearly delineated on the skull (compare to the atlanto-occipital joints). lar disk. The mandibular fossa is a depression in the squamous part of The external auditory canal lies just posterior to the mandibular fossa. the temporal bone, bounded by an articular tubercle and a postglenoid Trauma to the mandible may damage the auditory canal. Head (condyle) of mandible Pterygoid Joint fovea capsule Neck of Coronoid mandible Lateral process ligament Neck of mandible Lingula Mandibular Stylomandibular foramen ligament Mylohyoid groove AB Fig. 9.28 Head of the mandible in the TMJ Fig. 9.29 Ligaments of the lateral TMJ A Anterior view. B Posterior view. The head (condyle) of the mandible is Left lateral view. The TMJ is surrounded by a relatively lax capsule that markedly smaller than the mandibular fossa and has a cylindrical shape. permits physiological dislocation during jaw opening. The joint is stabi- Both factors increase the mobility of the mandibular head, allowing lized by three ligaments: lateral, stylomandibular, and sphenomandib- rotational movements about a vertical axis. -
Human Jaw Motion Simulator
Human Jaw Motion Simulator MIMU702 Technical Design Report Human Jaw Motion Simulator Project #05 Final Report Design Advisor: Prof. Muftu Design Team Bryan Galer, Nathaniel Hockenberry, James Maloof, Mia Monte-Lowrey, Katelyn O’Donnell April 17, 2007 Department of Mechanical, Industrial and Manufacturing Engineering College of Engineering, Northeastern University Boston, MA 02115 HUMAN JAW MOTION SIMULATOR Design Team Bryan Galer, Nathaniel Hockenberry, James Maloof, Mia Monte-Lowrey, Katelyn O’Donnell Design Advisor / Sponsor Professor Sinan Muftu Abstract The following report describes the anatomy and biomechanics of the human jaw along with design ideas for the development of a realistic jaw simulator. Creating a physical simulation gives hope that controls can be applied to study the jaw’s mechanical properties, dynamic loadings, joint thresholds, and joint degeneration. This knowledge could lead to the ability to test and improve current jaw prosthetics or even to the eventual understanding and treatment of the temporomandibular joint (TMJ) disease. The problems that exist in creating a realistic simulator are the unknown order, direction, and magnitude of muscle forces, the functions of the various ligaments, and the complex TMJ. The project has been broken down into four stages, with the goal of this first stage being simulation of jaw closing. In order to accomplish this goal, three muscles were used: the temporal, the masseter, and the lateral pterygoid muscles. This will be accomplished using servo motors to act as the muscles. The system control is position-based rather than force-based, a decision that was made because the force equations were statically indeterminate. A LabVIEW interface was created to control the position of the jaw and monitor the lengths of each muscle group.