Anatomy of Meninges
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Multiple Osteomas of the Falx Cerebri and Anterior Skull Base: Case Report
CASE REPORT J Neurosurg 124:1339–1342, 2016 Multiple osteomas of the falx cerebri and anterior skull base: case report Khaled M. Krisht, MD,1 Cheryl A. Palmer, MD,2 and William T. Couldwell, MD, PhD1 1Department of Neurosurgery, Clinical Neurosciences Center, and 2Department of Pathology, University of Utah, Salt Lake City, Utah The authors describe a rare case of intracranial extraaxial parafalcine and anterior skull base osteomas in a 22-year- old woman presenting with bifrontal headaches. This case highlights the possible occurrence of such lesions along the anterior skull base and parafalcine region that, as such, should be considered as part of the differential diagnosis for extraaxial calcific lesions involving the anterior skull base. To the authors’ knowledge, this is the first reported case of a patient who underwent complete successful resection of multiple extraaxial osteomas of the anterior skull base and parafalcine region. http://thejns.org/doi/abs/10.3171/2015.6.JNS15865 KEY WORDS osteoma; anterior skull base; parafalcine; falx cerebri; differential; CT; oncology STEOMAS are benign neoplasms consisting of ma- was first evaluated 6 years earlier, undergoing contrast- ture normal osseous tissue. They commonly arise enhancing MRI of the brain that disclosed a nonenhanc- from the long bones of the extremities. In the re- ing extraaxial T1-weighted isointense and T2-weighted Ogion of the head and neck, they are usually limited to the hypointense parafalcine lesion. At her latest presentation paranasal sinuses, facial bones, skull, and mandible.4,5,7 repeat brain MRI with and without contrast enhancement Their etiology is still a matter of debate. -
Why Do Bridging Veins Rupture Into the Virtual Subdural Space?
J Neurol Neurosurg Psychiatry: first published as 10.1136/jnnp.47.2.121 on 1 February 1984. Downloaded from Journal of Neurology, Neurosurgery, and Psychiatry 1984;47:121-127 Why do bridging veins rupture into the virtual subdural space? T YAMASHIMA, RL FRIEDE From the Department ofNeuropathology, University of Gottingen, Gottingen, Federal Republic of Germany SUMMARY Electron microscopic data on human bridging veins show thin walls of variable thick- ness, circumferential arrangement of collagen fibres and a lack of outer reinforcement by arach- noid trabecules, all contributory to the subdural portion of the vein being more fragile than its subarachnoid portion. These features explain the laceration of veins and the subdural location of resultant haematomas. Most subdural haematomas due to venous bleeding walls are delicate, lacking muscle fibres, with only a have been attributed to lacerations in bridging veins. thin fibrous wall and a thin elastic lamina adjacent to These veins form short trunks passing directly from the endothelial layer. The conclusions of these two the brain to the dura mater, almost at right angles to authors, have gained wide acceptance, although guest. Protected by copyright. both. Between these two points, bridging veins take there was little evidence concerning the fragility of a straight course with no tortuosity to allow for the the vein walls. possible displacement of brain.' Trotter2 speculated The purpose of the present communication is to that subdural haematomas are invariably due to provide electron microscopic data on tissue fixed in trauma tearing large veins, an interpretation situ, which might throw some light on to the lacera- elaborated by Krauland.3 According to Leary,4 the tion mechanism of bridging veins and its relationship common sources of subdural haematomas are rup- to the development of subdural haematoma. -
Distance Learning Program Anatomy of the Human Brain/Sheep Brain Dissection
Distance Learning Program Anatomy of the Human Brain/Sheep Brain Dissection This guide is for middle and high school students participating in AIMS Anatomy of the Human Brain and Sheep Brain Dissections. Programs will be presented by an AIMS Anatomy Specialist. In this activity students will become more familiar with the anatomical structures of the human brain by observing, studying, and examining human specimens. The primary focus is on the anatomy, function, and pathology. Those students participating in Sheep Brain Dissections will have the opportunity to dissect and compare anatomical structures. At the end of this document, you will find anatomical diagrams, vocabulary review, and pre/post tests for your students. The following topics will be covered: 1. The neurons and supporting cells of the nervous system 2. Organization of the nervous system (the central and peripheral nervous systems) 4. Protective coverings of the brain 5. Brain Anatomy, including cerebral hemispheres, cerebellum and brain stem 6. Spinal Cord Anatomy 7. Cranial and spinal nerves Objectives: The student will be able to: 1. Define the selected terms associated with the human brain and spinal cord; 2. Identify the protective structures of the brain; 3. Identify the four lobes of the brain; 4. Explain the correlation between brain surface area, structure and brain function. 5. Discuss common neurological disorders and treatments. 6. Describe the effects of drug and alcohol on the brain. 7. Correctly label a diagram of the human brain National Science Education -
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. -
The Strain Rates in the Brain, Brainstem, Dura, and Skull Under Dynamic Loadings
Mathematical and Computational Applications Article The Strain Rates in the Brain, Brainstem, Dura, and Skull under Dynamic Loadings Mohammad Hosseini-Farid 1,2,* , MaryamSadat Amiri-Tehrani-Zadeh 3, Mohammadreza Ramzanpour 1, Mariusz Ziejewski 1 and Ghodrat Karami 1 1 Department of Mechanical Engineering, North Dakota State University, Fargo, ND 58104, USA; [email protected] (M.R.); [email protected] (M.Z.); [email protected] (G.K.) 2 Department of Orthopedic Surgery, Mayo Clinic, Rochester, MN 55905, USA 3 Department of Computer Science, North Dakota State University, Fargo, ND 58104, USA; [email protected] * Correspondence: [email protected]; Tel.: +1-7012315859 Received: 7 March 2020; Accepted: 5 April 2020; Published: 7 April 2020 Abstract: Knowing the precise material properties of intracranial head organs is crucial for studying the biomechanics of head injury. It has been shown that these biological tissues are significantly rate-dependent; hence, their material properties should be determined with respect to the range of deformation rate they experience. In this paper, a validated finite element human head model is used to investigate the biomechanics of the head in impact and blast, leading to traumatic brain injuries (TBI). We simulate the head under various directions and velocities of impacts, as well as helmeted and unhelmeted head under blast shock waves. It is demonstrated that the strain rates for the brain 1 are in the range of 36 to 241 s− , approximately 1.9 and 0.86 times the resulting head acceleration under impacts and blast scenarios, respectively. The skull was found to experience a rate in the range 1 of 14 to 182 s− , approximately 0.7 and 0.43 times the head acceleration corresponding to impact and blast cases. -
MR of the Diaphragma Sellae
765 MR of the Diaphragma Sellae David L. Daniels 1 The appearance of the diaphragma sellae is described in cryomicrotomic sections Kathleen W. Pojunas1 and on MR in patients with and without intra- and suprasellar masses. On MR, it appears David P. Kilgore 1 as a thin band of negligible signal that is best shown when adjacent CSF or a mass has Peter Pech 2 greater signal intensity. Its position or absence can be used to differentiate intrasellar Glenn A. Meyer masses with suprasellar components from suprasellar masses. Alan L. Williams 1 1 Victor M. Haughton Differentiating intrasellar masses with suprasellar components from suprasellar masses may be difficult with CT because the pituitary gland, diaphragma sellae, and suprasellar masses may enhance equally after intravenous contrast adminis tration. Theoretically, MR should be able to show the diaphragma sellae because other dural reflections, such as the falx cerebri and walls of the cavernous sinuses, can be differentiated from the adjacent CSF when it has greater signal intensity [1 ]. Materials and Methods Sagittal or coronal anatomic images of the sella were obtained by sectioning four fresh frozen cadaver heads with a horizontally cutting heavy-duty sledge cryomicrotome (LKB 2250) and then serially photographing the surfaces of the specimens [2]. In the anatomic images, the diaphragma sellae and associated blood vessels, the pituitary gland, and the infundibulum were identified using anatomic literature [3-5]. Ten normal volunteers and 22 patients were studied with MR . The patients included 12 with pituitary microadenomas that were verified by surgical findings (four cases) and by CT, clinical , and chemical findings [6]; seven with pituitary macroadenomas and two with tuber culum sellae meningiomas that were verified by CT and surgery; and one with a large suprasellar aneurysm that was verified by CT and angiography. -
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. -
What to Expect After Having a Subarachnoid Hemorrhage (SAH) Information for Patients and Families Table of Contents
What to expect after having a subarachnoid hemorrhage (SAH) Information for patients and families Table of contents What is a subarachnoid hemorrhage (SAH)? .......................................... 3 What are the signs that I may have had an SAH? .................................. 4 How did I get this aneurysm? ..................................................................... 4 Why do aneurysms need to be treated?.................................................... 4 What is an angiogram? .................................................................................. 5 How are aneurysms repaired? ..................................................................... 6 What are common complications after having an SAH? ..................... 8 What is vasospasm? ...................................................................................... 8 What is hydrocephalus? ............................................................................... 10 What is hyponatremia? ................................................................................ 12 What happens as I begin to get better? .................................................... 13 What can I expect after I leave the hospital? .......................................... 13 How will the SAH change my health? ........................................................ 14 Will the SAH cause any long-term effects? ............................................. 14 How will my emotions be affected? .......................................................... 15 When should -
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. -
Why Woodpecker Can Resist the Impact
Why woodpecker can resist the impact A thesis submitted in fulfilment of the requirements for the degree of Doctor of Philosophy Zhe Zhang Master of Civil Engineering, RMIT University, Melbourne, Australia School of Engineering College of Science, Engineering and Health RMIT University November 2019 II Declaration I certify that except where due acknowledgement has been made, the work is that of the author alone; the work has not been submitted previously, in whole or in part, to qualify for any other academic award; the content of the thesis is the result of work which has been carried out since the official commencement date of the approved research program; any editorial work, paid or unpaid, carried out by a third party is acknowledged; and ethics procedures and guidelines have been followed. Zhe Zhang 30 November 2019 III Acknowledgments The research in this thesis could not have been completed without significant support from many individuals and organisations. I would like to take this opportunity to express my deep gratitude to all of them. Firstly, I would like to express my sincere gratitude to my senior supervisor, Dr. Shiwei Zhou, for his wisdom in choosing this fascinating research topic for me and his constant encouragement and guidance. After the guidance of my Master graduation project, Dr. Zhou accepted me as one of the Ph.D. students and offered financial support for my first-year study at RMIT University. He has always been patient in providing guidance and offering supportive suggestions to me during my PhD candidature period. It is not an exaggeration to say that he has changed my life and his good characteristics have had a significant and positive impact on me which would be beneficial for the rest of my life. -
Meninges Ventricles And
Meninges ,ventricles & CSF Dr.Sanaa Al-Shaarawy Dr. Essam Eldin Salama OBJECTIVES • By the end of the lecture the student should be able to: • Describe the cerebral meninges & list the main dural folds. • Describe the spinal meninges & locate the level of the termination of each of them. • Describe the importance of the subarachnoid space. • List the Ventricular system of the CNS and locate the site of each of them. • Describe the formation, circulation, drainage, and functions of the CSF. • Know some clinical point about the CSF MENINGES • The brain and spinal cord are invested by three concentric membranes ; • The outermost layer is the dura matter. • The middle layer is the arachnoid matter. • The innermost layer is the pia matter. DURA MATER ▪The cranial dura is a two layered tough, fibrous thick membrane that surrounds the brain. ▪It is formed of two layers; periosteal and meningeal. ▪The periosteal layer is attached to the skull. ▪The meningeal layer is folded forming the dural folds : falx cerebri, and tentorium cerebelli. ▪Sensory innervation of the dura is mostly from : meningeal branches of the trigeminal and vagus nerves & C1 to C3(upper cervical Ns.). DURA MATER Folds Two large reflection of dura extend into the cranial cavity : 1.The falx cerebri, In the midline, ▪It is a vertical sickle-shaped sheet of dura, extends from the cranial roof into the great longitudinal fissure between the two cerebral hemispheres. ▪It has an attached border adherent to the skull. ▪And a free border lies above the corpus callosum. DURA MATER Folds 2. A horizontal shelf of dura, The tentorium cerebelli, ▪ It lies between the posterior part of the cerebral hemispheres and the cerebellum. -
Intimate Exchange Between Cerebrospinal Fluid and Interstitial Fluid May Contribute to Maintenance of Homeostasis in the Central Nervous System
REVIEW ARTICLE doi: 10.2176/nmc.ra.2016-0020 Neurol Med Chir (Tokyo) 56, 416–441, 2016 Online May 27, 2016 Research into the Physiology of Cerebrospinal Fluid Reaches a New Horizon: Intimate Exchange between Cerebrospinal Fluid and Interstitial Fluid May Contribute to Maintenance of Homeostasis in the Central Nervous System Mitsunori MATSUMAE,1 Osamu SATO,2 Akihiro HIRAYAMA,1 Naokazu HAYASHI,1 Ken TAKIZAWA,1 Hideki ATSUMI,1 and Takatoshi SORIMACHI1 1Department of Neurosurgery, Tokai University School of Medicine, Isehara, Kanagawa; 2Tokai University, Shibuya, Tokyo Abstract Cerebrospinal fluid (CSF) plays an essential role in maintaining the homeostasis of the central nervous system. The functions of CSF include: (1) buoyancy of the brain, spinal cord, and nerves; (2) volume ad- justment in the cranial cavity; (3) nutrient transport; (4) protein or peptide transport; (5) brain volume regulation through osmoregulation; (6) buffering effect against external forces; (7) signal transduction; (8) drug transport; (9) immune system control; (10) elimination of metabolites and unnecessary substances; and finally (11) cooling of heat generated by neural activity. For CSF to fully mediate these functions, fluid-like movement in the ventricles and subarachnoid space is necessary. Furthermore, the relation- ship between the behaviors of CSF and interstitial fluid in the brain and spinal cord is important. In this review, we will present classical studies on CSF circulation from its discovery over 2,000 years ago, and will subsequently introduce functions that were recently discovered such as CSF production and absorp- tion, water molecule movement in the interstitial space, exchange between interstitial fluid and CSF, and drainage of CSF and interstitial fluid into both the venous and the lymphatic systems.