Enlarged Superior Cervical Sympathetic Ganglion Mimicking a Metastatic Lymph Node in the Retropharyngeal Space: a Case Report 인두후공간의 전이림프절로 오인된 비대 상경부교감신경절: 증례 보고
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Autonomic Nervous System
AUTONOMIC NERVOUS SYSTEM PAGE 1 AUTONOMIC NERVOUS SYSTEM PAGE 2 AUTONOMIC NERVOUS SYSTEM PAGE 3 AUTONOMIC NERVOUS SYSTEM PAGE 4 AUTONOMIC NERVOUS SYSTEM PAGE 5 AUTONOMIC NERVOUS SYSTEM PAGE 6 AUTONOMIC NERVOUS SYSTEM PAGE 7 AUTONOMIC NERVOUS SYSTEM PAGE 8 AUTONOMIC NERVOUS SYSTEM PAGE 9 REVIEW QUESTIONS 1. The autonomic nervous system controls the activity of _?_. (a) smooth muscle (b) cardiac muscle (c) glands (d) all of these (e) none of these 2. All preganglionic and postganglionic autonomic neurons are _?_ neurons. (a) somatic efferent (b) visceral efferent (c) somatic afferent (d) visceral afferent (e) association neurons 3. Which neurotransmitter is released at the synapses between preganglionic and postganglionic autonomic neurons ? (a) epinephrine (b) norepinephrine (c) acetylcholine (d) serotonin (e) oxytocin 4. All preganglionic sympathetic neurons are located in: (a) the lateral horn of the spinal cord of spinal cord segments T1-L2 (b) brainstem nuclei (c) intramural (terminal) ganglia (d) paravertebral ganglia of the sympathetic chains (e) prevertebral ganglia 5. All preganglionic parasympathetic neurons are located in _?_. (a) prevertebral ganglia (b) the lateral horn of spinal cord segments T1-L2 (c) sympathetic chain ganglia (d) intramural ganglia (e) brainstem nuclei and spinal cord segments S2-S4 6. Prevertebral and paravertebral ganglia contain _?_. (a) preganglionic sympathetic neurons (b) preganglionic parasympathetic neurons (c) postganglionic sympathetic neurons (d) postganglionic parasympathetic neurons (e) all of these 7. The otic, ciliary, submandibular and pterygopalatine ganglia are located in the head region and contain _?_. (a) preganglionic sympathetic neurons (b) preganglionic parasympathetic neurons (c) postganglionic sympathetic neurons (d) postganglionic parasympathetic neurons (e) none of these 8. -
Nervous System Central Nervous System Peripheral Nervous System Brain Spinal Cord Sensory Division Motor Division Somatic Nervou
Autonomic Nervous System Organization of Nervous System: Nervous system Integration Central nervous system Peripheral nervous system (CNS) (PNS) Motor Sensory output input Brain Spinal cord Motor division Sensory division (Efferent) (Afferent) “self governing” Autonomic Nervous System Somatic Nervous System (Involuntary; smooth & (Voluntary; skeletal muscle) cardiac muscle) Stability of internal environment depends largely on this system Marieb & Hoehn – Figure 14.2 Autonomic Nervous System Ganglion: Comparison of Somatic vs. Autonomic: A group of cell bodies located in the PNS Cell body Effector location NTs organs Effect CNS Single neuron from CNS to effector organs ACh + Stimulatory Heavily myelinated axon Somatic NS Somatic Skeletal muscle ACh = Acetylcholine Two-neuron chain from CNS to effector organs CNS ACh Ganglion NE Postganglionic axon Preganglionic axon (unmyelinated) (lightly myelinated) Sympathetic + Stimulatory Autonomic NS Autonomic or inhibitory CNS Ganglion (depends ACh ACh on NT and NT receptor Smooth muscle, Type) Postganglionic glands, cardiac Preganglionic axon axon muscle Parasympathetic (lightly myelinated) (unmyelinated) NE = Norepinephrine 1 Autonomic Nervous System Organization of Nervous System: Nervous system Integration Central nervous system Peripheral nervous system (CNS) (PNS) Motor Sensory output input Brain Spinal cord Motor division Sensory division (Efferent) (Afferent) Autonomic Nervous System Somatic Nervous System (Involuntary; smooth & (Voluntary; skeletal muscle) cardiac muscle) Sympathetic division -
The Neuroanatomy of Female Pelvic Pain
Chapter 2 The Neuroanatomy of Female Pelvic Pain Frank H. Willard and Mark D. Schuenke Introduction The female pelvis is innervated through primary afferent fi bers that course in nerves related to both the somatic and autonomic nervous systems. The somatic pelvis includes the bony pelvis, its ligaments, and its surrounding skeletal muscle of the urogenital and anal triangles, whereas the visceral pelvis includes the endopelvic fascial lining of the levator ani and the organ systems that it surrounds such as the rectum, reproductive organs, and urinary bladder. Uncovering the origin of pelvic pain patterns created by the convergence of these two separate primary afferent fi ber systems – somatic and visceral – on common neuronal circuitry in the sacral and thoracolumbar spinal cord can be a very dif fi cult process. Diagnosing these blended somatovisceral pelvic pain patterns in the female is further complicated by the strong descending signals from the cerebrum and brainstem to the dorsal horn neurons that can signi fi cantly modulate the perception of pain. These descending systems are themselves signi fi cantly in fl uenced by both the physiological (such as hormonal) and psychological (such as emotional) states of the individual further distorting the intensity, quality, and localization of pain from the pelvis. The interpretation of pelvic pain patterns requires a sound knowledge of the innervation of somatic and visceral pelvic structures coupled with an understand- ing of the interactions occurring in the dorsal horn of the lower spinal cord as well as in the brainstem and forebrain. This review will examine the somatic and vis- ceral innervation of the major structures and organ systems in and around the female pelvis. -
Autonomic Nervous System ANS 1 Introduction
Autonomic Nervous System ANS 1 Introduction Control the visceral function = arterial pressure = gastrointestinal motility and secretion = urinary bladder emptying = sweating = body temperature Sympathetic • Divisions of ANS : Division Parasympathetic Division ANS: Preganglionic fibers Postganglionic fibers The Autonomic nervous system Activated by centers located in: • -the spinal cord • - brain stem • - hypothalamus • - the limbic cortex • - The Autonomic nervous system operates by means of visceral reflexes - The efferent Autonomic signals are transmitted to the body through two major subdivisions called - The sympathetic nervous system . - The parasympathetic nervous system. Sympathetic Division Physiological Anatomy of the sympathetic nervous system - two para vertebral sympathetic chains of ganglia in sides of the spinal column - two pre vertebral ganglia inside the abdomen and nervous extending from the ganglia to the different internal organs - the sympathetic nervous originate in the spinal cord between the segments T1 - L2 and pass from here first in to the sympathetic chain and then to the tissues and organs The cell body of each pre ganglion nervous lies in the inter media lateral from of the spinal cord , and its fibers passes through an anterior root of the cord and the spinal nerve. The pre ganglion sympathetic fibers leave the nerve and pass into one of the ganglia of the sympathetic chain Sympathetic Ganglia: A - Paravertebral or Sympathetic chain ganglia B - Prevertebral or Collateral ganglia C - Terminal or Peripheral -
Ganglion of Impar Block
Ganglion of Impar Block A ganglion of impar block is safe and easy procedure used to treat visceral, pelvic, genital, perineal and anal pain. This injection is considered to be a type of sympathetic block that can be used in the treatment of sympathetically-mediated pain, pain secondary to malignancy, neuropathic pain and post- surgical pain. Patients who will benefit from this blockade will frequently present with vague and poorly localized pain in the “seat” region, which is burning in character and frequently accompanied by sensations of urgency with urination and/or defecation.[1] The target in the procedure is the ganglion of impar – also known as the ganglion of Walther or sacrococcygeal ganglion. It is a singular retroperitoneal structure located at the level of the sacrococcygeal junction (SCJ). There are 4 or 5 small sacral ganglia with the ganglion Impar being the most caudal segment of the confluence of the sacral sympathetic chain as it passes anteromedially over the sacrum. More specifically, the ganglion Impar is the terminal fusion of the 2 sacral sympathetic chains and is located with some anatomical variability between the SCJ and the lower segment of the first coccyx. The fusion of the 2 chains typically positions the ganglion midline, which makes it relatively easy to find. However, there is a wide range of variability in the anatomical location with respect to the SCJ.[2] This structure is of particular importance when considering patients who suffer from pain in the pelvic and perineal structures as it provides nociceptive and sympathetic supply to those regions. It receives afferent innervation from: Perineum Distal rectum Anus Distal urethra Distal vagina Vulva Coccyx Scrotum The block is performed by injecting a small amount of anesthetic onto the ganglion of impar, signals of the sympathetic nervous system (SNS) and pain fibers are interrupted from multiple structures simultaneously, leading to dramatic pain relief. -
CVM 6100 Veterinary Gross Anatomy
2010 CVM 6100 Veterinary Gross Anatomy General Anatomy & Carnivore Anatomy Lecture Notes by Thomas F. Fletcher, DVM, PhD and Christina E. Clarkson, DVM, PhD 1 CONTENTS Connective Tissue Structures ........................................3 Osteology .........................................................................5 Arthrology .......................................................................7 Myology .........................................................................10 Biomechanics and Locomotion....................................12 Serous Membranes and Cavities .................................15 Formation of Serous Cavities ......................................17 Nervous System.............................................................19 Autonomic Nervous System .........................................23 Abdominal Viscera .......................................................27 Pelvis, Perineum and Micturition ...............................32 Female Genitalia ...........................................................35 Male Genitalia...............................................................37 Head Features (Lectures 1 and 2) ...............................40 Cranial Nerves ..............................................................44 Connective Tissue Structures Histologic types of connective tissue (c.t.): 1] Loose areolar c.t. — low fiber density, contains spaces that can be filled with fat or fluid (edema) [found: throughout body, under skin as superficial fascia and in many places as deep fascia] -
Development of the Rat Superior Cervical Ganglion: Initial Stages of Synapse Formation’
0270.6474/0503-0697$02.00/O The Journal of Neuroscience Copyright 0 Society for Neuroscience Vol. 5. No. 3, pp. 697-704 Printed in U.S.A. March 1985 Development of the Rat Superior Cervical Ganglion: Initial Stages of Synapse Formation’ ERIC RUBIN* Department of Physiology and Biophysics, Washington University School of Medicine, St. Louis, Missouri 63110 Abstract some aspects of synaptic organization through the prenatal period. Some of these results have been briefly reported (Rubin, 1982). Synapse formation in the rat superior cervical ganglion has been investigated electrophysiologically and at the ultra- Materials and Methods structural level. Preganglionic axons first enter the superior The procedures for obtaining and isolating fetal rats have been described cervical ganglion between days 12 and 13 of gestation (El2 (Rubin 1985a, b). As in the previous papers, the day of conception is counted to E13), and on El3 a postganglionic response can be evoked as embryonic day zero (EO), and the first postnatal day is termed PO. by preganglionic stimulation. The susceptibility of this re- flectrophysiology. In isolated fetuses, the right superior cervical ganglion sponse to fatigue and to blocking agents indicates that it is was exposed, along with the internal carotid nerve and the cervical sympa- mediated by cholinergic synapses. On E14, the overall thetic trunk (see Rubin, 1985a). The dissection was carried out at room strength of ganglionic innervation arising from different temperature in a standard Ringer’s solution (pH 7.2) of the following com- spinal segments already varies in a pattern resembling that position (in millimolar concentration): NaCI, 137.0; KCI, 4.0; MgCIP, 1.0; found in maturity. -
Nervous System Central Nervous System Peripheral Nervous System Brain Spinal Cord Sensory Division Motor Division Somatic Nervou
Autonomic Nervous System Organization of Nervous System: Nervous system Integration Central nervous system Peripheral nervous system (CNS) (PNS) Motor Sensory output input Brain Spinal cord Motor division Sensory division (Efferent) (Afferent) “self governing” Autonomic Nervous System Somatic Nervous System (Involuntary; smooth & (Voluntary; skeletal muscle) cardiac muscle) Stability of internal environment depends largely on this system Marieb & Hoehn – Figure 14.2 Autonomic Nervous System Ganglion: Comparison of Somatic vs. Autonomic: A group of cell bodies located in the PNS Cell body Effector location NTs organs Effect CNS Single neuron from CNS to effector organs ACh + Stimulatory Heavily myelinated axon Somatic NS Somatic Skeletal muscle ACh = Acetylcholine Two-neuron chain from CNS to effector organs CNS ACh Ganglion NE Postganglionic axon Preganglionic axon (unmyelinated) (lightly myelinated) Sympathetic + Stimulatory Autonomic NS Autonomic or inhibitory CNS Ganglion (depends ACh ACh on NT and NT receptor Smooth muscle, Type) Postganglionic glands, cardiac Preganglionic axon axon muscle Parasympathetic (lightly myelinated) (unmyelinated) NE = Norepinephrine Autonomic Nervous System Organization of Nervous System: Nervous system Integration Central nervous system Peripheral nervous system (CNS) (PNS) Motor Sensory output input Brain Spinal cord Motor division Sensory division (Efferent) (Afferent) Autonomic Nervous System Somatic Nervous System (Involuntary; smooth & (Voluntary; skeletal muscle) cardiac muscle) Sympathetic division -
Specific Targeting of Ganglion Cell Sprouts Provides an Additional
The Journal of Neuroscience, October 1, 1998, 18(19):7987–7995 Specific Targeting of Ganglion Cell Sprouts Provides an Additional Mechanism for Restoring Peripheral Motor Circuits in Pelvic Ganglia after Spinal Nerve Damage Mark E. Kepper and Janet R. Keast Department of Physiology and Pharmacology, The University of Queensland, St. Lucia, Queensland, 4072, Australia The pelvic ganglia contain both sympathetic and parasympa- which grow profusely within just a few days. These arise from thetic neurons and provide an interesting model in which to each of the main chemical classes of pelvic neurons but grow study the effects of a distributed spinal nerve lesion. Previous at different rates and have different distributions. Importantly, animal studies have suggested that after either lumbar or sacral some chemical classes of sprouts preferentially supply neurons nerve injury, some functional connections are restored between of dissimilar histochemistry, suggesting the presence of very preganglionic and postganglionic neurons. It has been pro- specific targeting mechanisms rather than random growth. posed that this is because of intact preganglionic axons sprout- These sprouts are transient, however, those formed after partial ing collaterals to supply denervated ganglion cells. However, decentralization appear to be maintained. Moreover, after le- this has never been demonstrated, and our study has investi- sion of either lumbar or sacral spinal nerves, many sprouts arise gated whether the ganglion cells themselves contribute to axo- from neurons with intact spinal connections and innervate neu- genesis and restoration of peripheral circuitry. We have moni- rons that have lost their preganglionic inputs. This provides a tored the growth of axons from pelvic ganglion cells after very different alternative mechanism to reestablish communi- lumbar or sacral nerve injury (partial decentralization), or a cation between preganglionic and postganglionic neurons. -
THE ANATOMY of the SYMPATHETHIC TRUNKS in MAN by MARTIN WRETE Histological Department, the University of Uppsala, Sweden
[ 448 ] THE ANATOMY OF THE SYMPATHETHIC TRUNKS IN MAN BY MARTIN WRETE Histological Department, The University of Uppsala, Sweden INTRODUCTION Even a cursory study of the anatomical descriptions of the cervical parts of the sympathetic trunks given in modern text-books or articles discloses that, now as earlier, great confusion exists with respect to terminology. This applies even to monographs and more specialized presentations. The primary cause of this confusion is the very marked variability of the trunks in the neck region, which gives wide scope for arbitrary interpretations of the arrangement; some uncertainty about the terminology and notation of other parts of the trunks also persists. It is true that the terms to be used for the sympathetic nervous system were fixed by the International Anatomical Nomenclature Committee (Nomina Anatomica, Paris, 1955). This does not, however, prevent some of the individual terms being used to denote different anatomical units, and for practical reasons (such as limiting printing costs) comprehensive explanations could not always be given in the annota- tions to the Parisian Nomina Anatomica. As one of the three members of the Sub- Committee responsible for the nomenclature of the peripheral nervous system, I wish to define more exactly my views on the terminology adopted for the sympathetic trunks. I also take this opportunity of revising a few terms I used in certain papers published some twenty years ago. In Nomina Anatomica the term truncus sympathicus is followed by the names of its ganglia, ganglia trunci sympathici, as well as of its connecting rami interganglio- nares. But, also under the heading ganglia trunci sympathici, the term ganglia intermedia is used to denote ganglia on the rami communicantes and certain ganglia on the trunks in the rami interganglionares between the other ganglia-namely the ganglion cervicale superius, ganglion cervicale medium, ganglion cervicothoracicum (s. -
Plasticity of Neurons in Mouse Major Pelvic Ganglia in Response to Loss of Physiological
Plasticity of neurons in mouse major pelvic ganglia in response to loss of physiological input in cases of nerve injury and spinal cord injury A Dissertation Presented to The Faculty of the Graduate School At the University of Missouri In Partial Fulfillment Of the Requirements for the Degree Doctor of Philosophy By Cindy Kyi Dr. David Schulz, Dissertation Advisor May 2018 i The undersigned, appointed by the dean of the Graduate School, have examined the dissertation entitled PLASTICITY OF NEURONS IN MOUSE MAJOR PELVIC GANGLIA IN RESPONSE TO LOSS OF PHYSIOLOGICAL INPUT IN CASES OF NERVE INJURY AND SPINAL CORD INJURY Presented by Kyi, Cindy (MU-Student) A candidate for the degree of Doctor of Philosophy And hereby certify that, in their opinion, it is worthy of acceptance. Dr. David J. Schulz Dr. Michael L. Garcia Dr. Andrew D. McClellan Dr. Kevin J. Cummings Dedicated to Mom and Dad iii ACKNOWLEDGEMENTS First of all, I would like to thank God for guiding me and being with me and my family since the day I left Myanmar (Burma). He has been my rock and shelter through all the challenges along the way. I am very grateful to my advisor Dr. David Schulz for granting me with the opportunity to work in his laboratory and believing in me to take on a new project. Thank you very much for all your guidance, patience, training, and for giving me room to grow under your mentorship. I would also like to thank my committee members Dr. Andrew McClellan, Dr. Michael Garcia, and Dr. Kevin Cummings for all of their support in providing me with feedback not only on the details of experimental protocols but also helping me relate my experimental findings to a big picture context. -
Introduction to the Peripheral Nervous System 2
Introduction to the 2 Peripheral Nervous System toward the neuron’s cell body, and an axon is the long process CONTENTS that carries the action potential away from the cell body. INTRODUCTION Some neurons appear to have only a single process extending PERIPHERAL NERVOUS SYSTEM from only one pole (a differentiated region of the cell body) SPINAL CORD (CENTRAL NERVOUS SYSTEM) that divides into two parts (Fig. 2-1). This type of neuron is OVERVIEW OF THE AUTONOMIC NERVOUS SYSTEM called a pseudounipolar neuron because embryonically it Sympathetic Nervous System develops from a bipolar neuroblast in which the two axons Parasympathetic Nervous System fuse. Multipolar neurons (Fig. 2-2) have multiple dendrites Visceral Afferent Neurons and typically a single axon arising from an enlarged portion REFERRED PAIN of the cell body called the axon hillock. These processes CLASSIFICATION OF NEURONAL FIBERS extend from different poles of the cell body. One neuron communicates with other neurons or glands DEVELOPMENT OF THE SPINAL CORD AND or muscle cells across a junction between cells called a PERIPHERAL NERVOUS SYSTEM synapse. Typically, communication is transmitted across a synapse by means of specific neurotransmitters, such as acetylcholine, epinephrine, and norepinephrine, but in some cases in the CNS by means of electric current passing ●●● INTRODUCTION from cell to cell. Many axons are ensheathed with a substance called The nervous system comprises the central nervous system myelin, which acts as an insulator. Myelinated axons transmit (CNS) and the peripheral nervous system (PNS). The CNS is impulses much faster than nonmyelinated axons. Myelin surrounded and protected by the skull (neurocranium) and consists of concentric layers of lipid-rich material formed vertebral column and consists of the brain and the spinal by the plasma membrane of a myelinating cell.