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Prognostic Implications of Total Hemispheric Glucose Metabolism
Journal of Nuclear Medicine, published on October 27, 2016 as doi:10.2967/jnumed.116.180398 Prognostic Implications of Total Hemispheric Glucose Metabolism Ratio in Cerebro-Cerebellar Diaschisis *Eivind Antonsen Segtnan1,2, Peter Grupe1, Jens Ole Jarden3, Oke Gerke1,4,Jana Ivanidze5 Sofie Bæk Christlieb1, Caius Constantinescu1, John Erling Pedersen1, Sina Houshmand6, Søren Hess1,7,8 Mojtaba Zarei9, Albert Gjedde2,10, Abass Alavi6, Poul F. Høilund-Carlsen1,8 1Department of Nuclear Medicine, Odense University Hospital, Odense, Denmark 2 University of Southern Denmark, Odense, Denmark 3Department of Neurology, Herlev University Hospital, Copenhagen, Denmark 4Centre of Health Economics Research, Odense, University of Southern Denmark, Denmark 5Department of Diagnostic Radiology, Weill Cornell Medical College, NewYork-Presbyterian Hospital, New York, NY, United States 6Division of Nuclear Medicine, Department of Radiology, Perelman School of Medicine, Hospital of the University of Pennsylvania, Philadelphia, PA, USA 7Department of Radiology and Nuclear Medicine, Hospital of Southwest Jutland, Esbjerg, Denmark 8Department of Clinical Research, Faculty of Health Sciences, University of Southern Denmark, Odense, Denmark 9National Brain Mapping Centre, Shahid Beheshti University (Medical and General Campus), Tehran, Iran. 10Department of Neuroscience and Pharmacology, Panum Institute, University of Copenhagen, Copenhagen, Denmark 1 *Corresponding author Eivind Antonsen Segtnan ( Medicin student) , Allegade 34, 2.tv, 5000 Odense C, Denmark, Tel: +45 3044 8498, e-mail: [email protected] 2 Abstract Purpose: Diaschisis denotes brain dysfunction remote from a focal brain lesion. We have quantified diaschisis and investigated its prognostic value in glioma. Methods and material: We compared 50 18F-FDG-PET-CT studies collected prospectively from 14 patients with supratentorial glioma (5 men and 9 women aged 35-77 years) with 10 single scans from healthy controls aged 43-75 years. -
Review Article Meninges: from Protective Membrane to Stem Cell Niche
Am J Stem Cell 2012;1(2):92-105 www.AJSC.us /ISSN: 2160-4150/AJSC1205003 Review Article Meninges: from protective membrane to stem cell niche Ilaria Decimo1, Guido Fumagalli1, Valeria Berton1, Mauro Krampera2, Francesco Bifari2 1Department of Public Health and Community Medicine, Section of Pharmacology, University of Verona, Italy; 2De- partment of Medicine, Stem Cell Laboratory, Section of Hematology, University of Verona, Italy Received May 16, 2012; accepted May 23, 2012; Epub 28, 2012; Published June 30, 2012 Abstract: Meninges are a three tissue membrane primarily known as coverings of the brain. More in depth studies on meningeal function and ultrastructure have recently changed the view of meninges as a merely protective mem- brane. Accurate evaluation of the anatomical distribution in the CNS reveals that meninges largely penetrate inside the neural tissue. Meninges enter the CNS by projecting between structures, in the stroma of choroid plexus and form the perivascular space (Virchow-Robin) of every parenchymal vessel. Thus, meninges may modulate most of the physiological and pathological events of the CNS throughout the life. Meninges are present since the very early em- bryonic stages of cortical development and appear to be necessary for normal corticogenesis and brain structures formation. In adulthood meninges contribute to neural tissue homeostasis by secreting several trophic factors includ- ing FGF2 and SDF-1. Recently, for the first time, we have identified the presence of a stem cell population with neural differentiation potential in meninges. In addition, we and other groups have further described the presence in men- inges of injury responsive neural precursors. In this review we will give a comprehensive view of meninges and their multiple roles in the context of a functional network with the neural tissue. -
Endoscopic Anatomical Study of the Arachnoid Architecture on the Base of the Skull
DOI 10.1515/ins-2012-0005 Innovative Neurosurgery 2013; 1(1): 55–66 Original Research Article Peter Kurucz* , Gabor Baksa , Lajos Patonay and Nikolai J. Hopf Endoscopic anatomical study of the arachnoid architecture on the base of the skull. Part I: The anterior and middle cranial fossa Abstract: Minimally invasive neurosurgery requires a Introduction detailed knowledge of microstructures, such as the arach- noid membranes. In spite of many articles addressing The arachnoid was discovered and named by Gerardus arachnoid membranes, its detailed organization is still not Blasius in 1664 [ 22 ]. Key and Retzius were the first who well described. The aim of this study is to investigate the studied its detailed anatomy in 1875 [ 11 ]. This description was topography of the arachnoid in the anterior cranial fossa an anatomical one, without mentioning clinical aspects. The and the middle cranial fossa. Rigid endoscopes were intro- first clinically relevant study was provided by Liliequist in duced through defined keyhole craniotomies, to explore 1959 [ 13 ]. He described the radiological anatomy of the sub- the arachnoid structures in 110 fresh human cadavers. We arachnoid cisterns and mentioned a curtain-like membrane describe the topography and relationship to neurovascu- between the supra- and infratentorial cranial space bearing lar structures and suggest an intuitive terminology of the his name still today. Lang gave a similar description of the arachnoid. We demonstrate an “ arachnoid membrane sys- subarachnoid cisterns in 1973 [ 12 ]. With the introduction of tem ” , which consists of the outer arachnoid and 23 inner microtechniques in neurosurgery, the detailed knowledge arachnoid membranes in the anterior fossa and the middle of the surgical anatomy of the cisterns became more impor- fossa. -
Nervous System - PNS and CNS
Nervous System - PNS AND CNS Locate the following structures on the appropriate model or diagram. Understand the function of ea Neuron Spinal nerves Cerebrum axon cervical plexus cerebral hemisphere dendrite phrenic cerebral cortex cell body gray matter Schwann cell brachial plexus white matter node of Ranvier axillary gyrus (convolution) myelin sheath radial longitudinal fissure neurolemma median falx cerebri Nissl bodies ulnar central sulcus synaptic knobs lateral sulcus synaptic vesicles lumbar plexus frontal lobe femoral parietal lobe Spinal Cord obturator occipital lobe central canal temporal lobe posterior column sacral plexus insula lateral column sciatic corpus callosum anterior column tibial olfactory bulb posterior sulcus common fibular olfactory tract anterior fissure superficial fibular posterior horn deep fibular Diencephalon lateral horn thalamus anterior horn intercostal nerves intermediate mass gray commissure hypothalamus conus medularis Autonomic NS infundibulum dorsal nerve root sympathetic trunk pituitary gland dorsal root ganglion ganglia (paravertebral) pineal gland ventral nerve root mammillary bodies spinal nerve Brainstem optic nerve cauda equina = medulla, pons, mid, optic tract filum terminale cranial nerves optic chiasm Meninges Midbrain dura mater cerebral peduncles Cranial Nerves dural sinus superior colliculus I olfactory epidural space inferior colliculus II optic arachnoid mater III oculomotor subarachnoid space Pons IV trochlear arachnoid granulations (villi) V trigeminal pia mater Medulla Oblongata VI abducens choroid plexus pyramids VII facial denticulate ligament olive VIII vestibulocochlear IX glossopharyngeal Cerebellum X vagus Ventricles cerebellar hemisphere XI accessory lateral ventricles vermis XII hypoglossal septum pellucidum transverse fissure third ventricle tentorium cerebelli cerebral aqueduct falx cerebelli fourth ventricle arbor vitae. -
A Cellular Atlas of the Developing Meninges Reveals Meningeal Fibroblast Diversity and Function
bioRxiv preprint doi: https://doi.org/10.1101/648642; this version posted May 24, 2019. The copyright holder for this preprint (which was not certified by peer review) is the author/funder. All rights reserved. No reuse allowed without permission. 1 2 3 4 Title: A cellular atlas of the developing meninges reveals meningeal fibroblast diversity and function 5 6 Authors: John DeSisto1,2,3,, Rebecca O’Rourke2, Stephanie Bonney1,3, Hannah E. Jones1,3, Fabien 7 Guimiot4, Kenneth L. Jones2 and Julie A. Siegenthaler1,3,5 8 9 1Department of Pediatrics Section of Developmental Biology, 2Department of Pediatrics Section of 10 Section of Hematology, Oncology, Bone Marrow Transplant, 3Cell Biology, Stem Cells and Development 11 Graduate Program, University of Colorado, Anschutz Medical Campus, Aurora, CO 80045 USA, 12 4INSERM UMR 1141, Hôpital Robert Debré, 75019 Paris, France. 13 14 5Corresponding Author: 15 Julie A. Siegenthaler, PhD 16 University of Colorado, School of Medicine 17 Department of Pediatrics 18 12800 East 19th Ave MS-8313 19 Aurora, CO 80045 USA 20 Telephone #: 303-724-3123 21 E-mail: [email protected] 22 23 Key words (3-6 words): brain development, meninges, pial basement membrane, retinoic acid, human 24 meninges bioRxiv preprint doi: https://doi.org/10.1101/648642; this version posted May 24, 2019. The copyright holder for this preprint (which was not certified by peer review) is the author/funder. All rights reserved. No reuse allowed without permission. 25 Abstract 26 The meninges, a multilayered structure that encases the CNS, is composed mostly of fibroblasts, 27 along with vascular and immune cells. -
87.MANISH KUMAR DOI.Cdr
Volume - 10 | Issue - 12 | December - 2020 | PRINT ISSN No. 2249 - 555X | DOI : 10.36106/ijar Review Article Dentistry THE MANDIBULAR NERVE, ITS COURSE, ANATOMICAL VARIATIONS AND PTERYGOMANDIBULAR SPACE. - A SYSTEMATIC REVIEW. Assistant Professor, Department Of Dentistry, Government Medical College & Dr. Manish Kumar Hospital, Ratlam (M.P). Dr. Kapil Associate Professor, Department Of Dentistry, Ananta Institute Of Medical Sciences Karwasra* And Research Centre, Rajsamand, Rajasthan. *Corresponding Author Dr. Amit Senior Resident, Department Of Dentistry, Sardar Patel Medical College & Associated Chhaparwal Hospital, Bikaner, (Rajasthan). ABSTRACT Knowledge of mandibular nerve and its branches is important when performing dental and surgical procedures of mandible. So, this systematic review article revealed all details of mandibular nerve course and also important anatomical variations. Mandibular nerve during its course go through the pterygomandibular space and this space is important for inferior alveolar nerve block anaesthesia, so all details of pterygomandibular structure are also included in this review. KEYWORDS : Mandibular Nerve, Pterygomandibular Space, Inferior Alveolar Nerve, Trigeminal Nerve, Trigeminal Ganglion. INTRODUCTION and this site is generally used for buccal nerve block 5. The trigeminal nerve (TN) exits the brain on the lateral surface of pons, entering the trigeminal ganglion (TGG) after few millimeters, Deep temporal nerves usually are two nerves, anterior and posterior. followed by an extensive series of divisions1. Mandibular nerve (MN) They pass between the skull and the LPt, and enter the deep surface of is the largest of the three divisions of trigeminal nerve. MN also temporalis2. contains motor or efferent bers to innervate the muscles that are attached to mandible. Most of these bers travel directly to their target The nerve to LPt enters the deep surface of the muscle and may arise tissues. -
Associations of Pathological Diagnosis and Genetic Abnormalities In
www.nature.com/scientificreports OPEN Associations of pathological diagnosis and genetic abnormalities in meningiomas with the embryological origins of the meninges Atsushi Okano1, Satoru Miyawaki1*, Hiroki Hongo1, Shogo Dofuku1, Yu Teranishi1, Jun Mitsui2, Michihiro Tanaka3, Masahiro Shin1, Hirofumi Nakatomi1 & Nobuhito Saito1 Certain driver mutations and pathological diagnoses are associated with the anatomical site of meningioma, based on which the meninges have diferent embryological origins. We hypothesized that mutations and pathological diagnoses of meningiomas are associated with diferent embryological origins. We comprehensively evaluated associations among tumor location, pathological diagnosis (histological type), and genetic alterations including AKT1, KLF4, SMO, POLR2A, and NF2 mutations and 22q deletion in 269 meningioma cases. Based on the embryological origin of meninges, the tumor locations were as follows: neural crest, paraxial mesodermal, and dorsal mesodermal origins. Tumors originating from the dura of certain embryologic origin displayed a signifcantly diferent pathological diagnoses and genetic abnormality ratio. For instance, driver genetic mutations with AKT1, KLF4, SMO, and POLR2A, were signifcantly associated with the paraxial mesodermal origin (p = 1.7 × 10−10). However, meningiomas with NF2-associated mutations were signifcantly associated with neural crest origin (p = 3.9 × 10–12). On analysis of recurrence, no diference was observed in embryological origin. However, POLR2A mutation was a risk factor for the tumor recurrence (p = 1.7 × 10−2, Hazard Ratio 4.08, 95% Confdence Interval 1.28–13.0). Assessment of the embryological origin of the meninges may provide novel insights into the pathomechanism of meningiomas. Meningiomas are the most common primary intracranial tumors accounting for 20% of all such tumors. -
Trigeminal Cave and Ganglion: an Anatomical Review
Int. J. Morphol., 31(4):1444-1448, 2013. Trigeminal Cave and Ganglion: An Anatomical Review Cavo y Ganglio Trigeminal: Una Revisión Anatómica N. O. Ajayi*; L. Lazarus* & K. S. Satyapal* AJAYI, N. O.; LAZARUS, L. & SATYAPAL, K. S. Trigeminal cave and ganglion: an anatomical review. Int. J. Morphol., 31(4):1444- 1448, 2013. SUMMARY: The trigeminal cave (TC) is a special channel of dura mater, which extends from the posterior cranial fossa into the posteromedial portion of the middle cranial fossa at the skull base. The TC contains the motor and sensory roots of the trigeminal nerve, the trigeminal ganglion (TG) as well as the trigeminal cistern. This study aimed to review the anatomy of the TC and TG and determine some parameters of the TC. The study comprised two subsets: A) Cadaveric dissection on 30 sagitally sectioned formalin fixed heads and B) Volume injection. We found the dura associated with TC arranged in three distinct layers. TC had relations with internal carotid artery, the cavernous sinus, the superior petrosal sinus, the apex of petrous temporal bone and the endosteal dura of middle cranial fossa. The mean volume of TC was 0.14 ml. The mean length and breadth of TG were 18.3 mm and 7.9 mm, respectively, mean width and height of trigeminal porus were 7.9 mm and 4.1 mm, respectively, and mean length of terminal branches from TG to point of exit within skull was variable. An understanding of the precise formation of the TC, TG, TN and their relations is important in order to perform successful surgical procedures and localized neural block in the region of the TC. -
Study of the Brain ...Pdf
Sudan University of Sciences and Technology College of Graduate Studies Study of the Brain Structures Development During Childhood Using Magnetic Resonance Imaging دراسة تطورتركيب الذماغ في مرحلة الطفولة باستخذام التصوير بالرنين المغناطيسي A Thesis submitted for Fulfillment of the Requirement of Master Degree (M. Sc) in Diagnostic Radiological Technology By: Suhair Talha Ibrahim Shaheen Supervisor: Prof. Caroline Edward Ayad Khilla (2019) I اٜٚخ الْشَأْثِبسْىِ سَثِّكَ انّزِ٘ خَهَكَ * خَهَ كَ اﻹَِْسَبٌَ يٍِْ عَهَكٍ * الْشَأَْٔسَثُّكَ اﻷَكْشَوُ * انّزِ٘ عَهّىَ ثِبنْمَهَىِ * عَهّىَ اﻹَِْسَبٌ َيَبنَى َْٚعْهَىْ )سٕسحانعهك: -1.5) صذق اهلل انعظٛى I Dedication To my parents To my family To all my friends To colleagues for their love and support. II Acknowledgment First of all, I thank Allah the Almighty for helping me complete this study. I thank Professor Caroline Edward Ayad Khilla, my supervisor, for her help and guidance. Thanks a lot, and all grateful for her. I would like to express my gratitude to Doctor Heba Tolab a medical radiologist at the Saudi Germen hospital. She lent a hand to getting samples Attention to the importance of research and what they aspire to, and all research samples were diagnosed as normal by her. I would like to thank Doctor Khalid Abdlhafith head of the of Radiology Technicians Department at the International Medical Center hospital by extending a helping hand to provide me samples for research. Finally I would like to thank everybody who helped me prepare and finish this study. III Abstract This is a descriptive analytical study, the study population composed of normal brain patients presenting to the Magnetic resonance unit. -
Frontal Lobe Anterior Corpora Commissure Quadrigemina Superior Colliculus Optic Chiasm Inferior Colliculus
Chapter 16 The Nervous System The Brain and Cranial Nerves Lecture Presentation by Steven Bassett Southeast Community College © 2015 Pearson Education, Inc. Introduction • The brain is a complex three-dimensional structure that performs a bewildering array of functions • Think of the brain as an organic computer • However, the brain is far more versatile than a computer • The brain is far more complex than the spinal cord • The brain consists of roughly 20 billion neurons © 2015 Pearson Education, Inc. An Introduction to the Organization of the Brain • Embryology of the Brain • The CNS begins as a neural tube • The lumen of the tube (neurocoel) is filled with fluid • The lumen of the tube will expand thus forming the various ventricles of the brain • In the fourth week of development, the cephalic area of the neural tube enlarges to form: • Prosencephalon • Mesencephalon • Rhombencephalon © 2015 Pearson Education, Inc. Table 16.1 Development of the Human Brain © 2015 Pearson Education, Inc. An Introduction to the Organization of the Brain • Embryology of the Brain (continued) • Prosencephalon eventually develops to form: • Telencephalon forms: • Cerebrum • Diencephalon forms: • Epithalamus, thalamus, and hypothalamus. © 2015 Pearson Education, Inc. Table 16.1 Development of the Human Brain © 2015 Pearson Education, Inc. An Introduction to the Organization of the Brain • Embryology of the Brain (continued) • Mesencephalon • Does not subdivide • Becomes the midbrain © 2015 Pearson Education, Inc. Table 16.1 Development of the Human Brain © 2015 Pearson Education, Inc. An Introduction to the Organization of the Brain • Embryology of the Brain (continued) • Rhombencephalon • Eventually develops to form: • Metencephalon: forms the pons and cerebellum • Myelencephalon: forms the medulla oblongata © 2015 Pearson Education, Inc. -
Malignant CNS Solid Tumor Rules
Malignant CNS and Peripheral Nerves Equivalent Terms and Definitions C470-C479, C700, C701, C709, C710-C719, C720-C725, C728, C729, C751-C753 (Excludes lymphoma and leukemia M9590 – M9992 and Kaposi sarcoma M9140) Introduction Note 1: This section includes the following primary sites: Peripheral nerves C470-C479; cerebral meninges C700; spinal meninges C701; meninges NOS C709; brain C710-C719; spinal cord C720; cauda equina C721; olfactory nerve C722; optic nerve C723; acoustic nerve C724; cranial nerve NOS C725; overlapping lesion of brain and central nervous system C728; nervous system NOS C729; pituitary gland C751; craniopharyngeal duct C752; pineal gland C753. Note 2: Non-malignant intracranial and CNS tumors have a separate set of rules. Note 3: 2007 MPH Rules and 2018 Solid Tumor Rules are used based on date of diagnosis. • Tumors diagnosed 01/01/2007 through 12/31/2017: Use 2007 MPH Rules • Tumors diagnosed 01/01/2018 and later: Use 2018 Solid Tumor Rules • The original tumor diagnosed before 1/1/2018 and a subsequent tumor diagnosed 1/1/2018 or later in the same primary site: Use the 2018 Solid Tumor Rules. Note 4: There must be a histologic, cytologic, radiographic, or clinical diagnosis of a malignant neoplasm /3. Note 5: Tumors from a number of primary sites metastasize to the brain. Do not use these rules for tumors described as metastases; report metastatic tumors using the rules for that primary site. Note 6: Pilocytic astrocytoma/juvenile pilocytic astrocytoma is reportable in North America as a malignant neoplasm 9421/3. • See the Non-malignant CNS Rules when the primary site is optic nerve and the diagnosis is either optic glioma or pilocytic astrocytoma. -
Volume 1: the Upper Extremity
Volume 1: The Upper Extremity 1.1 The Shoulder 01.00 - 38.20 (37.20) 1.1.1 Introduction to shoulder section 0.01.00 0.01.28 0.28 1.1.2 Bones, joints, and ligaments 1 Clavicle, scapula 0.01.29 0.05.40 4.11 1.1.3 Bones, joints, and ligaments 2 Movements of scapula 0.05.41 0.06.37 0.56 1.1.4 Bones, joints, and ligaments 3 Proximal humerus 0.06.38 0.08.19 1.41 Shoulder joint (glenohumeral joint) Movements of shoulder joint 1.1.5 Review of bones, joints, and ligaments 0.08.20 0.09.41 1.21 1.1.6 Introduction to muscles 0.09.42 0.10.03 0.21 1.1.7 Muscles 1 Long tendons of biceps, triceps 0.10.04 0.13.52 3.48 Rotator cuff muscles Subscapularis Supraspinatus Infraspinatus Teres minor Teres major Coracobrachialis 1.1.8 Muscles 2 Serratus anterior 0.13.53 0.17.49 3.56 Levator scapulae Rhomboid minor and major Trapezius Pectoralis minor Subclavius, omohyoid 1.1.9 Muscles 3 Pectoralis major 0.17.50 0.20.35 2.45 Latissimus dorsi Deltoid 1.1.10 Review of muscles 0.20.36 0.21.51 1.15 1.1.11 Vessels and nerves: key structures First rib 0.22.09 0.24.38 2.29 Cervical vertebrae Scalene muscles 1.1.12 Blood vessels 1 Veins of the shoulder region 0.24.39 0.27.47 3.08 1.1.13 Blood vessels 2 Arteries of the shoulder region 0.27.48 0.30.22 2.34 1.1.14 Nerves The brachial plexus and its branches 0.30.23 0.35.55 5.32 1.1.15 Review of vessels and nerves 0.35.56 0.38.20 2.24 1.2.