Congenital Spondylolytic Spondylolisthesis of Cervical Spine - a Case Report and Review of the Literature
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Low Back Pain in Adolescent Athletes
Low back pain in Adolescent Athletes Claes Göran Sundell Department of Community Medicine and Rehabilitation Umeå 2019 Responsible publischer under Swedish law: The Dean of the Medical Faculty This work is protected by the Swedish Copyright Legislation (Act 1960:729) Dissertation for PhD ISBN: 978-91-7855-024-1 ISSN-0346-6612 New series no: 2014 Copyright © Claes Göran Sundell, 2019 Cover illustration: Stina Norgren, Illustre.se Illustrations: Stina Norgren, Illustre.se, page 1,3,4,12,13,41 Illustration page 2: Permission Encyplopedica Brittanica, page 2 Pictures: 3D4 Medical; www.3D4Medical.com, page 1,3,5,6,7 Article nr .3 "© Georg Thieme Verlag KG." All previously published papers were reproduced with the kind permission of the publishers Electronic version available at: http://umu.diva-portal.org/ Printed by: UmU Print Service, Umeå University Umeå, Sweden, 2019 1 “Listen to the Sound of Silence” Unknown To my family: Doris, Cecilia, David, Johan Contents Abstract .......................................................................................... iv Sammanfattning på svenska ........................................................... vi Preface .......................................................................................... viii Abbreviations ................................................................................. ix Introduction .................................................................................... 1 1.Anatomy ........................................................................................................................ -
Pars Injection for Lumbar Spondylolysis
Pars Injection for Lumbar Spondylolysis Issue 4: March 2016 Review date: February 2019 Following your recent investigations and consultation with your spinal surgeon, a possible cause for your symptoms may have been found. Your X-rays and / or scans have revealed that you have a lumbar spondylolysis. This is a stress fracture of the narrow bridge of bone between the facet joints (pars interarticularis) at the back of the spine, commonly called a pars defect. There may be a hereditary aspect to spondylolysis, for example an individual may be born with thin vertebral bone and therefore be vulnerable to this condition; or certain sports, such as gymnastics, weight lifting and football can put a great deal of stress on the bones through constantly over-stretching the spine. Either cause can result in a stress fracture on one or both sides of the vertebra (bone of the spine). Many people are not aware of their stress fracture or experience any problems but symptoms can occasionally occur including lower back pain, pain in the thighs and buttocks, stiffness, muscle tightness and tenderness. vertebra facet joint pars interarticularis sacrum spondylolysis (pars defect) intervertebral disc If the stress fracture weakens the bone so much that it is unable to maintain its proper position, the vertebra can start to shift out of place. This condition is called spondylolisthesis. Page 3 There is a forward slippage of one lumbar vertebra on the vertebra below it. The degree of spondylolisthesis may vary from mild to severe but if too much slippage occurs, the nerve roots can be stretched where they branch out of the spinal canal. -
Pushing the Limits of Prenatal Ultrasound: a Case of Dorsal Dermal Sinus Associated with an Overt Arnold–Chiari Malformation and a 3Q Duplication
reproductive medicine Case Report Pushing the Limits of Prenatal Ultrasound: A Case of Dorsal Dermal Sinus Associated with an Overt Arnold–Chiari Malformation and a 3q Duplication Olivier Leroij 1, Lennart Van der Veeken 2,*, Bettina Blaumeiser 3 and Katrien Janssens 3 1 Faculty of Medicine, University of Antwerp, 2610 Wilrijk, Belgium; [email protected] 2 Department of Obstetrics and Gynaecology, University Hospital Antwerp, 2650 Edegem, Belgium 3 Department of Medical Genetics, University Hospital and University of Antwerp, 2650 Edegem, Belgium; [email protected] (B.B.); [email protected] (K.J.) * Correspondence: [email protected] Abstract: We present a case of a fetus with cranial abnormalities typical of open spina bifida but with an intact spine shown on both ultrasound and fetal MRI. Expert ultrasound examination revealed a very small tract between the spine and the skin, and a postmortem examination confirmed the diagnosis of a dorsal dermal sinus. Genetic analysis found a mosaic 3q23q27 duplication in the form of a marker chromosome. This case emphasizes that meticulous prenatal ultrasound examination has the potential to diagnose even closed subtypes of neural tube defects. Furthermore, with cerebral anomalies suggesting a spina bifida, other imaging techniques together with genetic tests and measurement of alpha-fetoprotein in the amniotic fluid should be performed. Citation: Leroij, O.; Van der Veeken, Keywords: dorsal dermal sinus; Arnold–Chiari anomaly; 3q23q27 duplication; mosaic; marker chro- L.; Blaumeiser, B.; Janssens, K. mosome Pushing the Limits of Prenatal Ultrasound: A Case of Dorsal Dermal Sinus Associated with an Overt Arnold–Chiari Malformation and a 3q 1. -
Evicore Spine Imaging Guidelines
CLINICAL GUIDELINES Spine Imaging Policy Version 2.1 Effective October 1, 2020 eviCore healthcare Clinical Decision Support Tool Diagnostic Strategies:This tool addresses common symptoms and symptom complexes. Imaging requests for individuals with atypical symptoms or clinical presentations that are not specifically addressed will require physician review. Consultation with the referring physician, specialist and/or individual’s Primary Care Physician (PCP) may provide additional insight. CPT® (Current Procedural Terminology) is a registered trademark of the American Medical Association (AMA). CPT® five digit codes, nomenclature and other data are copyright 2020 American Medical Association. All Rights Reserved. No fee schedules, basic units, relative values or related listings are included in the CPT® book. AMA does not directly or indirectly practice medicine or dispense medical services. AMA assumes no liability for the data contained herein or not contained herein. © 2020 eviCore healthcare. All rights reserved. Spine Imaging Guidelines V2.1 Spine Imaging Guidelines Procedure Codes Associated with Spine Imaging 3 SP-1: General Guidelines 5 SP-2: Imaging Techniques 14 SP-3: Neck (Cervical Spine) Pain Without/With Neurological Features (Including Stenosis) and Trauma 22 SP-4: Upper Back (Thoracic Spine) Pain Without/With Neurological Features (Including Stenosis) and Trauma 26 SP-5: Low Back (Lumbar Spine) Pain/Coccydynia without Neurological Features 29 SP-6: Lower Extremity Pain with Neurological Features (Radiculopathy, Radiculitis, or Plexopathy and Neuropathy) With or Without Low Back (Lumbar Spine) Pain 33 SP-7: Myelopathy 37 SP-8: Lumbar Spine Spondylolysis/Spondylolisthesis 40 SP-9: Lumbar Spinal Stenosis 43 SP-10: Sacro-Iliac (SI) Joint Pain, Inflammatory Spondylitis/Sacroiliitis and Fibromyalgia 45 SP-11: Pathological Spinal Compression Fractures 48 SP-12: Spinal Pain in Cancer Patients 50 SP-13: Spinal Canal/Cord Disorders (e.g. -
Autosomal Recessive Klippel-Feil Syndrome
J Med Genet: first published as 10.1136/jmg.19.2.130 on 1 April 1982. Downloaded from Journal ofMedical Genetics, 1982, 19, 130-134 Autosomal recessive Klippel-Feil syndrome ELIAS OLIVEIRA DA SILVA From the Departamento de Biologia Geral, SecCdo de Genetica, Universidade Federal de Pernambuco, and Instituto Materno-Infantil de Pernambuco (IMIP), Recife, Brazil SUMMARY An inbred kindred with 12 cases of Klippel-Feil syndrome (seven females and five males) is reported. Inheritance is undoubtedly autosomal recessive. The main characteristic of the syndrome is fusion of cervical vertebrae. In 1912, Klippel and Feill reported the first clinical Methods details and necropsy findings of a syndrome char- acterised by the triad short or absent neck, severe A total of 59 members of the family, including all limitation of head movement, and low posterior living affected persons (11), were clinically examined hairline. An Egyptian mummy (from 500 BC) is the and radiological studies were performed in eight oldest subject in whom Klippel-Feil syndrome has patients. The other three refused to submit to been seen.2 Another interesting observation is the x-ray examination. The patients ranged in age from similarity between the figure of an old man depicted 9 to 59 years. by the English painter William Blake (1757-1827) The genealogical data was collected with the co- and the appearance of persons with Klippel-Feil operation of people in four generations and, in case syndrome.3 The incidence of the syndrome is of doubtful information, it was checked with estimated at about 1 in 42 000 births.4 Some authors different members of the family. -
Cleidocranial Dysplasia with Spina Bifida: Case Report [I] Displasia Cleido-Craniana Com Espinha Bífida: Relato De Caso
ISSN 1807-5274 Rev. Clín. Pesq. Odontol., Curitiba, v. 6, n. 2, p. 179-184, maio/ago. 2010 Licenciado sob uma Licença Creative Commons [T] CleidoCranial dysplasia with spina bifida: case report [I] Displasia cleido-craniana com espinha bífida: relato de caso [A] Mubeen Khan[a], rai puja[b] [a] Professor and head of Department of Oral Medicine and Radiology Government Dental College and Research Institute, Bangalore - India. [b] Postgraduate student, Department of Oral Medicine and Radiology, Government Dental College and Research Institute, Bangalore - India, e-mail: [email protected] [R] abstract oBJeCtiVe: To present and discuss a case of a rare disease in a 35 year old otherwise healthy male Indian in origin reported to the Department of Oral Medicine and Radiology of the Dental College and Research Institute, Bangalore, India. disCUssion: The cleidocranial dysplasia is a rare disease which can occur either spontaneously (40%) or by an autosomal dominant inheritance. The dentists are, most of the times, the first professionals who patients look for to solve their problem, since there is a delay in the eruption and /or absence of permanent teeth. In the present case multiple missing teeth was the reason for patient’s visit to odontologist. ConClUsion: An early diagnosis allows proper orientation for the treatment, offering a better life quality for the patient. [P] Keywords: Cleidocranial dysplasia. Aplastic clavicles. Delayed eruption. Supernumerary teeth. Spina bifida. [B] Resumo OBJETIVO: Apresentar e discutir um caso de doença rara em paciente masculino, de 35 anos de idade, sadio, de modo geral, de origem indiana, que foi encaminhado ao Departamento de Medicina Bucal e Radiologia da Escola de Odontologia e Instituto de Pesquisa, Bangalore, Índia. -
Spina Bifida
A Guide for School Personnel Working With Students With Spina Bifida Developed by The Specialized Health Needs Interagency Collaboration Patty Porter, M.S. Barbara Obst, R.N. Andrew Zabel, Ph.D. In partnership between Kennedy Krieger Institute and the Maryland State Department of Education Division of Special Education/Early Intervention Services December 2009 A Guide for School Personnel Working With Students With Spina Bifida Developed by the Kennedy Krieger Institute in partnership with the Maryland State Department of Education, Division of Special Education/Early Intervention Services December 2009 This document was produced by the Maryland State Department of Education, Division of Special Education/Early Intervention Services through IDEA Part B Grant #H027A0900035A, U.S. Department of Education, Office of Special Education and Rehabilitative Services. The views expressed herein do not necessarily reflect the views of the U.S. Department of Education or any other federal agency and should not be regarded as such. The Division of Special Education/Early Intervention Services receives funding from the Office of Special Education Program, Office of Special Education and Rehabilitative Services, U.S. Department of Education. This document is copyright free. Readers are encouraged to share; however, please credit the MSDE Division of Special Education/Early Intervention Services and Kennedy Krieger Institute. The Maryland State Department of Education does not discriminate on the basis of race, color, sex, age, national origin, religion, disability, or sexual orientation in matters affecting employment or in providing access to programs. For inquiries related to Department policy, contact the Equity Assurance and Compliance Branch, Office of the Deputy State Superintendent for Administration, Maryland State Department of Education, 200 West Baltimore Street, 6th Floor, Baltimore, MD 21201-2595, 410-767-0433, Fax 410-767-0431, TTY/TDD 410-333-6442. -
Thoracolumbar Spine
Color Code Thoracolumbar Spine Important Doctors Notes By Biochemistry team Editing File Notes/Extra explanation Objectives At the end of the lecture, students should be able to: Distinguish the thoracic and lumbar vertebrae from each other and from vertebrae of the cervical region Describe the characteristic features of a thoracic and a lumbar vertebra. Compare the movements occurring in thoracic and lumbar regions. Describe the joints between the vertebral bodies and the vertebral arches. List and identify the ligaments of the intervertebral joints. Introduction to Vertebrae There are approximately 33 vertebrae which are subdivided into 5 groups based on morphology and location: cervical, thoracic, lumbar, sacral, and coccygeal. Typical Vertebra All typical vertebrae consist of a vertebral body and a posterior vertebral arch. o Vertebral body: • weight-bearing part. The size increases inferiorly as the amount of weight supported increases. o Vertebral arch: • Extending from the arch are a number of processes for muscle attachment Vertebral and articulation with adjacent bones. foramen • It consists of: 1. Two pedicles (towards the body) 2. Two lamina (towards the spine) 3. Spinous process 4. Transverse process 5. Superior and inferior articular processes. (for articulation with adjacent vertebra) The vertebral foramen is the hole in the middle of the vertebra. Collectively they form the vertebral canal through which the spinal cord passes. Normal Curvature Of The Human’s Vertebral Column The vertebral column is Curves of vertebral not straight, it only looks column can be divided straight from the into: posterior and anterior • Primary curves: view. Thoracic & sacral. It is curved as seen from the lateral views. -
Beyond Crayons
THE JEFFRAS’ PROGRAM THAT PROMOTES A HEALTHY SCHOOL ENVIRONMENT FOR STUDENTS WITH SPINA BIFIDA SECTION 504 PLAN Background Plan Objectives & Goals Spina Bifida is the most common permanently Successful integration of a child with Spina Bifida disabling birth defect in the United States. Spina into school sometimes requires changes in school Bifida occurs when the spine of the baby fails to equipment or the curriculum. In adapting the school close. This creates an opening, or lesion, on the setting for the child with Spina Bifida, architectural spinal column. This takes place during the first factors should be considered. Section 504 of the month of pregnancy when the spinal column and Rehabilitation Act of 1973 requires programs that brain, or neural tube, is formed. This happens before receive federal funding to make their facilities most women even know they are pregnant. Because accessible. This can occur through structural of the opening on the spinal column, the nerves in changes (for example, adding elevators or ramps) or the spinal column may be damaged and not work through schedule and location changes (for properly. This results in some degree of paralysis. example, offering a course on the ground floor). The higher the lesion is on the spinal column, the greater the paralysis. Surgery to close the spine is The Student has a recognized disability, Spina Bifida, generally done within hours after birth. Surgery helps that requires the accommodations and modifications to reduce the risk of infection and to protect the set out in this plan to ensure that the student has the spinal cord from greater damage. -
Lumbar Spondylolysis in Adolescent Athletes Joseph P
■ BRIEF REPORT Lumbar Spondylolysis in Adolescent Athletes Joseph P. Garry, MD, and John McShane, MD Greenville, North Carolina Lumbar spondylolysis is a common cause of low back pain in adolescent athletes. The early diagnosis and treat ment of this condition will result in decreased morbidity and an earlier return to full activity for most patients. We report a case of lumbar spondylolysis in an adolescent athlete and review current diagnosis and management of this condition. KEY WORDS. Spondylolysis; adolescent; back pain; athlete. (J Fam Pract 1998; 46:145-149) he national explosion of competitive athletics onset of the low back pain was insidious, without a his has led to increasing participation of adoles tory of trauma. At presentation, the pain was described cents in organized team sports. Up to one half as a sharp, right-sided, lower lumbar and buttock pain of boys and one fourth of girls between the brought on during soccer practice while running and ages of 14 and 17 participate in some form of kicking, and was relieved with rest. No radicular symp organizedT team sport.1 The increase in the number of toms were described. The patient denied any previous adolescent athletes has resulted in more adolescent low back pain. Past medical history was unremarkable. complaints of low back pain.2 The lifetime prevalence of Physical examination revealed painful palpation of low back pain among 11- to 17-year-olds in the United the lower right lumbar spine with bilateral paraspinal States is reported to be 30.4%.3 Often, many young ath muscle spasm. -
PE056 Spina Bifida
Spina Bifida What is Spina Bifida is also called a neural tube defect. It happens when the neural Spina Bifida? tube, which includes the brain and spine of the embryo, does not close. This happens during the first month of pregnancy, often before the mother knows she is pregnant. There are many forms of neural tube defects. Spina Bifida Occulta In this form, there is an opening in one or more of the bones (vertebrae) (oh-cull-tuh) that make up the spine. These openings can be seen by X-ray only. The spinal cord, nerves and skin covering are normal. In fact, up to 10% of all Americans may have this most mild form of the spina bifida. In most cases Spina Bifida Occulta causes no problems. Spina Bifida Aperta In these forms, the neural tube does not close, and parts of the bones (ay-per-tuh) (vertebrae) that make up the spine are missing. A cyst or lump pokes out from the opening in the spine. There are 2 types of spina bifida aperta: Meningocele (muh-ninge-oh-seal) The cyst is covered with skin and most of the time there is minimal, if any, paralysis. Most children with meningocele grow normally. Your child with meningocele should be checked for fluid on the brain (hydrocephalus) and bowel and bladder problems so they can be treated promptly. Meningomyelocele (muh-ninge-oh-my-uh-low-seal) This is the most severe form of neural tube defect. The open defect contains nerve roots of the spinal cord and the cord itself. -
Anencephalic Fetus with Craniospinal Rachischisis - Case Report
IP Indian Journal of Anatomy and Surgery of Head, Neck and Brain 2019;5(4):124–126 Content available at: iponlinejournal.com IP Indian Journal of Anatomy and Surgery of Head, Neck and Brain Journal homepage: www.innovativepublication.com Case Report Anencephalic fetus with craniospinal rachischisis - Case report Sangeeta S Kotrannavar1, Vijaykumar S Kotrannavar2,* 1Dept. of Anatomy, USM- KLE International Medical Programme, Belgaum, India 2Shri JGCHS Ayurvedic Medical College, Ghataprabha, Karnataka, India ARTICLEINFO ABSTRACT Article history: Anencephaly is a severe neural tube defect (NTD) caused by failure of closure in the cranial neuropore Received 04-12-2019 during fourth week of pregnancy. As a result, major portion of the brain, skull and scalp is absent. Accepted 22-12-2019 Anencephaly may be associated with rachischisis, where defective neural tube closure is extensive and Available online 24-01-2020 spinal cord is exposed. Overall incidence of anencephaly is one in every 1000 births. It can be easily diagnosed by ultrasonography. Anencephaly newborns are not viable nor treatable and classified as lethal NTDs. Nutritional and environmental factors play a role in production of NTDs. Here we report and Keywords: discuss a rare case of anencephalic fetus with craniospinal rachischisis of 25 weeks of gestation and their Anencephaly embryological origin. Neural tube defect Rachischisis © 2019 Published by Innovative Publication. This is an open access article under the CC BY-NC-ND license (https://creativecommons.org/licenses/by/4.0/) 1. Introduction forms brain and caudal part develops into spinal cord. NTDs result from abnormal closure of neural folds in third and Anencephaly is a congenital severe lethal neural tube fourth week of development.