New Insights in Lumbosacral Plexopathy
Total Page:16
File Type:pdf, Size:1020Kb
Load more
Recommended publications
-
Dental Plexopathy Vesta Guzeviciene, Ricardas Kubilius, Gintautas Sabalys
SCIENTIFIC ARTICLES Stomatologija, Baltic Dental and Maxillofacial Journal, 5:44-47, 2003 Dental Plexopathy Vesta Guzeviciene, Ricardas Kubilius, Gintautas Sabalys SUMMARY Aim and purpose of the study were: 1) to study and compare unfavorable factors playing role in the development of upper teeth plexitis and upper teeth plexopathy; 2) to study peculiarities of clinical manifestation of upper teeth plexitis and upper teeth plexopathy, and to establish their diagnostic value; 3) to optimize the treatment. The results of examination and treatment of 79 patients with upper teeth plexitis (UTP-is) and 63 patients with upper teeth plexopathy (UTP-ty) are described in the article. Questions of the etiology, pathogenesis and differential diagnosis are discussed, methods of complex medicamental and surgical treatment are presented. Keywords: atypical facial neuralgia, atypical odontalgia, atypical facial pain, vascular toothache. PREFACE Besides the common clinical tests, in order to ana- lyze in detail the etiology and pathogenesis of the afore- Usually the injury of the trigeminal nerve is re- mentioned disease, its clinical manifestation and pecu- lated to the pathology of the teeth neural plexuses. liarities, we performed specific examinations such as According to the literature data, injury of the upper orthopantomography of the infraorbital canals, mea- teeth neural plexuses makes more than 7% of all sured the velocity of blood flow in the infraorbital blood neurostomatologic diseases. Many terms are used in vessels (doplerography), examined the pain threshold literature to characterize the clinical symptoms com- of facial skin and oral mucous membrane in acute pe- plex of the above-mentioned pathology. Some authors riod and remission, and evaluated the role that the state (1, 2, 3) named it dental plexalgia or dental plexitis. -
Intrapartum Lesions to the Lumbar Portion of the Lumbosacral Plexus: an Anatomical Review
REVIEW Eur. J. Anat. 23 (2): 83-90 (2019) Intrapartum lesions to the lumbar portion of the lumbosacral plexus: an anatomical review Shanna E. Williams, Asa C. Black, Jr. Department of Biomedical Sciences, University of South Carolina School of Medicine Greenville, Greenville, SC, USA SUMMARY Key words: Plexopathy – Radiculopathy – Neu- The lumbosacral plexus is formed by the ventral ropathy – Pregnancy – Foot drop rami of L2-S3 and provides sensory and motor branches to the lower extremity. The spatial orien- INTRODUCTION tation of the lumbar portion of the plexus above the pelvic brim leaves it particularly susceptible to in- The lumbosacral plexus is formed by the ventral trapartum injury by the fetal head. Such lesions are rami of the L2-S3 segments, with some contribu- subdivided into two groups: upper lumbar plexus tions from L1 and S4 segments. It gives rise to six (L1-L4) and lumbosacral trunk (L4-L5). Given the sensory nerves of the thigh and leg, and six major root levels involved, upper lumbar plexus lesions sensorimotor nerves responsible for innervating 43 produce symptoms suggestive of iliohypogastric, muscles of the lower extremity (Van Alfen and ilioinguinal, genitofemoral, femoral, and obturator Malessy, 2013). As the name would suggest, it neuropathies or L4 radiculopathies. Alternatively, consists of two components, the lumbar plexus involvement of the lumbosacral trunk can imitate a and the sacral plexus, which are spatially separat- common fibular (peroneal) neuropathy or L5 ed. This anatomical separation results in a clinical radiculopathy. This symptomatic overlap with vari- division of lumbosacral plexus lesions into those ous neuropathies and radiculopathies, makes di- affecting the lumbar plexus and those affecting the agnosis of such lesions particularly challenging. -
Neurophysiologic Testing and Monitoring
UnitedHealthcare® Commercial Medical Policy Neurophysiologic Testing and Monitoring Policy Number: 2021T0493Z Effective Date: January 1, 2021 Instructions for Use Table of Contents Page Community Plan Policy Coverage Rationale ........................................................................... 1 • Neurophysiologic Testing and Monitoring Applicable Codes .............................................................................. 2 Description of Services ..................................................................... 4 Medicare Advantage Coverage Summary Clinical Evidence ............................................................................... 6 • Neurophysiological Studies U.S. Food and Drug Administration ..............................................16 References .......................................................................................18 Policy History/Revision Information..............................................21 Instructions for Use .........................................................................22 Coverage Rationale Nerve Conduction Studies The following are proven and medically necessary: • Nerve conduction studies with or without late responses (e.g., F-wave and H-reflex tests) and neuromuscular junction testing when performed in conjunction with needle electromyography for any of the following known or suspected disorders: o Peripheral neuropathy/polyneuropathy (e.g., inherited, metabolic, traumatic, entrapment syndromes) o Plexopathy o Neuromuscular junction disorders (e.g., -
Ischaemic Lumbosacral Plexopathy in Acute Vascular Compromise:Case Report
Parapkgia 29 (1991) 70-75 © 1991 International Medical Soci<ty of Paraplegia Paraplegia L-_________________________________________________ � Ischaemic Lumbosacral Plexopathy in Acute Vascular Compromise: Case Report D.X. Cifu, MD, K.D. Irani, MD Department of Physical Medicine, Baylor College of Medicine, Houston, Texas, USA. Summary Anterior spinal artery syndrome (ASAS) is a well reported cause of spinal cord injury (SCI) following thoracoabdominal aortic surgery. The resultant deficits are often incom plete, typically attributed to the variable nature of the vascular distribution. Our Physi cal Medicine and Rehabilitation (PM and Rehabilitation) service was consulted about a 36-year-old patient with generalised deconditioning, 3 months after a stab wound to the left ventricle. Physical examination revealed marked lower extremity weakness, hypo tonia, hyporeflexia, and a functioning bowel and bladder. Further questioning disclosed lower extremity dysesthesias. Nerve conduction studies showed slowed velocities, pro longed distal latencies and decreased amplitudes of all lower extremity nerves. Electro myography revealed denervation of all proximal and distal lower extremity musculature, with normal paraspinalis. Upper extremity studies were normal. Recently, 3 cases of ischaemic lumbosacral plexopathy, mimicking an incomplete SCI, have been reported. This distinction is particularly difficult in the poly trauma patient with multiple musculo skeletal injuries or prolonged recuperation time, in addition to a vascular insult, as in this patient. The involved anatomical considerations will be discussed. A review of the elec trodiagnostic data from 30 patients, with lower extremity weakness following acute ischaemia, revealed a 20% incidence of spinal cord compromise, but no evidence of a plexopathy. Key words: Ischaemia; Lumbosacral plexopathy; Electromyography. Recent advances in cardiovascular and trauma surgery have led to increased survi val of patients following cardiac and great vessel trauma or insult. -
Functional Annotation of Exon Skipping Event in Human Pora Kim1,*,†, Mengyuan Yang1,†,Keyiya2, Weiling Zhao1 and Xiaobo Zhou1,3,4,*
D896–D907 Nucleic Acids Research, 2020, Vol. 48, Database issue Published online 23 October 2019 doi: 10.1093/nar/gkz917 ExonSkipDB: functional annotation of exon skipping event in human Pora Kim1,*,†, Mengyuan Yang1,†,KeYiya2, Weiling Zhao1 and Xiaobo Zhou1,3,4,* 1School of Biomedical Informatics, The University of Texas Health Science Center at Houston, Houston, TX 77030, USA, 2College of Electronics and Information Engineering, Tongji University, Shanghai, China, 3McGovern Medical School, The University of Texas Health Science Center at Houston, Houston, TX 77030, USA and 4School of Dentistry, The University of Texas Health Science Center at Houston, Houston, TX 77030, USA Received August 13, 2019; Revised September 21, 2019; Editorial Decision October 03, 2019; Accepted October 03, 2019 ABSTRACT been used as therapeutic targets (3–8). For example, MET has lost the binding site of E3 ubiquitin ligase CBL through Exon skipping (ES) is reported to be the most com- exon 14 skipping event (9), resulting in an enhanced expres- mon alternative splicing event due to loss of func- sion level of MET. MET amplification drives the prolifera- tional domains/sites or shifting of the open read- tion of tumor cells. Multiple tyrosine kinase inhibitors, such ing frame (ORF), leading to a variety of human dis- as crizotinib, cabozantinib and capmatinib, have been used eases and considered therapeutic targets. To date, to treat patients with MET exon 14 skipping (10). Another systematic and intensive annotations of ES events example is the dystrophin gene (DMD) in Duchenne mus- based on the skipped exon units in cancer and cular dystrophy (DMD), a progressive neuromuscular dis- normal tissues are not available. -
A Database Integrating Genomic Indel Polymorphisms That Distinguish Mouse Strains Keiko Akagi1,2, Robert M
D600–D606 Nucleic Acids Research, 2010, Vol. 38, Database issue Published online 20 November 2009 doi:10.1093/nar/gkp1046 MouseIndelDB: a database integrating genomic indel polymorphisms that distinguish mouse strains Keiko Akagi1,2, Robert M. Stephens3, Jingfeng Li2,4, Evgenji Evdokimov5, Michael R. Kuehn5, Natalia Volfovsky3 and David E. Symer2,4,6,7,8,9,* 1Mouse Cancer Genetics Program, Center for Cancer Research, National Cancer Institute, Frederick, MD 21702, 2Department of Molecular Virology, Immunology and Medical Genetics, The Ohio State University Comprehensive Cancer Center, Columbus, OH 43210, 3Advanced Biomedical Computing Center, Information Systems Program, SAIC-Frederick, Inc., NCI-Frederick, Frederick, MD 21702, 4Basic Research Laboratory, 5Laboratory of Protein Dynamics and Signaling, 6Laboratory of Biochemistry and Molecular Biology, Center for Cancer Research, National Cancer Institute, Frederick, MD 21702, 7Human Cancer Genetics Program, 8Departments of Internal Medicine and 9Biomedical Informatics, The Ohio State University Comprehensive Cancer Center, Columbus, OH 43210, USA Received August 5, 2009; Revised October 23, 2009; Accepted October 27, 2009 ABSTRACT wide-ranging functional differences. This extensive phenotypic variation has helped to make the mouse a MouseIndelDB is an integrated database resource premier model organism, mimicking many aspects of containing thousands of previously unreported human diversity and diseases. Understanding the mouse genomic indel (insertion and deletion) genomic differences that -
Brachial-Plexopathy.Pdf
Brachial Plexopathy, an overview Learning Objectives: The brachial plexus is the network of nerves that originate from cervical and upper thoracic nerve roots and eventually terminate as the named nerves that innervate the muscles and skin of the arm. Brachial plexopathies are not common in most practices, but a detailed knowledge of this plexus is important for distinguishing between brachial plexopathies, radiculopathies and mononeuropathies. It is impossible to write a paper on brachial plexopathies without addressing cervical radiculopathies and root avulsions as well. In this paper will review brachial plexus anatomy, clinical features of brachial plexopathies, differential diagnosis, specific nerve conduction techniques, appropriate protocols and case studies. The reader will gain insight to this uncommon nerve problem as well as the importance of the nerve conduction studies used to confirm the diagnosis of plexopathies. Anatomy of the Brachial Plexus: To assess the brachial plexus by localizing the lesion at the correct level, as well as the severity of the injury requires knowledge of the anatomy. An injury involves any condition that impairs the function of the brachial plexus. The plexus is derived of five roots, three trunks, two divisions, three cords, and five branches/nerves. Spinal roots join to form the spinal nerve. There are dorsal and ventral roots that emerge and carry motor and sensory fibers. Motor (efferent) carries messages from the brain and spinal cord to the peripheral nerves. This Dorsal Root Sensory (afferent) carries messages from the peripheral to the Ganglion is why spinal cord or both. A small ganglion containing cell bodies of sensory NCS’s sensory fibers lies on each posterior root. -
Clinical Presentations of Lumbar Disc Degeneration and Lumbosacral Nerve Lesions
Hindawi International Journal of Rheumatology Volume 2020, Article ID 2919625, 13 pages https://doi.org/10.1155/2020/2919625 Review Article Clinical Presentations of Lumbar Disc Degeneration and Lumbosacral Nerve Lesions Worku Abie Liyew Biomedical Science Department, School of Medicine, Debre Markos University, Debre Markos, Ethiopia Correspondence should be addressed to Worku Abie Liyew; [email protected] Received 25 April 2020; Revised 26 June 2020; Accepted 13 July 2020; Published 29 August 2020 Academic Editor: Bruce M. Rothschild Copyright © 2020 Worku Abie Liyew. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. Lumbar disc degeneration is defined as the wear and tear of lumbar intervertebral disc, and it is mainly occurring at L3-L4 and L4-S1 vertebrae. Lumbar disc degeneration may lead to disc bulging, osteophytes, loss of disc space, and compression and irritation of the adjacent nerve root. Clinical presentations associated with lumbar disc degeneration and lumbosacral nerve lesion are discogenic pain, radical pain, muscular weakness, and cutaneous. Discogenic pain is usually felt in the lumbar region, or sometimes, it may feel in the buttocks, down to the upper thighs, and it is typically presented with sudden forced flexion and/or rotational moment. Radical pain, muscular weakness, and sensory defects associated with lumbosacral nerve lesions are distributed on -
4-Brachial Plexus and Lumbosacral Plexus (Edited).Pdf
Color Code Brachial Plexus and Lumbosacral Important Doctors Notes Plexus Notes/Extra explanation Please view our Editing File before studying this lecture to check for any changes. Objectives At the end of this lecture, the students should be able to : Describe the formation of brachial plexus (site, roots) List the main branches of brachial plexus Describe the formation of lumbosacral plexus (site, roots) List the main branches of lumbosacral plexus Describe the important Applied Anatomy related to the brachial & lumbosacral plexuses. Brachial Plexus Formation Playlist o It is formed in the posterior triangle of the neck. o It is the union of the anterior rami (or ventral) of the 5th ,6th ,7th ,8th cervical and the 1st thoracic spinal nerves. o The plexus is divided into 5 stages: • Roots • Trunks • Divisions • Cords • Terminal branches Really Tired? Drink Coffee! Brachial Plexus A P A P P A Brachial Plexus Trunks Divisions Cords o Upper (superior) trunk o o Union of the roots of Each trunk divides into Posterior cord: C5 & C6 anterior and posterior From the 3 posterior division divisions of the 3 trunks o o Middle trunk Lateral cord: From the anterior Continuation of the divisions of the upper root of C7 Branches and middle trunks o All three cords will give o Medial cord: o Lower (inferior) trunk branches in the axilla, It is the continuation of Union of the roots of the anterior division of C8 & T1 those will supply their respective regions. the lower trunk The Brachial Plexus Long Thoracic (C5,6,7) Anterior divisions Nerve to Subclavius(C5,6) Posterior divisions Dorsal Scapular(C5) Suprascapular(C5,6) upper C5 trunk Lateral Cord C6 middle (2LM) trunk C7 lower C8 trunk T1 Posterior Cord (ULTRA) Medial Cord (4MU) In the PowerPoint presentation this slide is animated. -
Lumbosacral Plexus Entrapment Syndrome. Part One: a Common Yet Little-Known Cause of Chronic Pelvic and Lower Extremity Pain
3-A Running head: ANAESTHESIA, PAIN & INTENSIVE CARE www.apicareonline.com ORIGINAL ARTICLE Lumbosacral plexus entrapment syndrome. Part one: A common yet little-known cause of chronic pelvic and lower extremity pain Kjetil Larsen, CES, George C. Chang Chien, D O2 ABSTRACT Corrective exercise specialist, Training & Rehabilitation, Oslo Lumbosacral plexus entrapment syndrome (LPES) is a little-known but common cause Norway of chronic lumbopelvic and lower extremity pain. The lumbar plexus, including the 2 Director of pain management, lumbosacral tunks emerge through the fibers of the psoas major, and the proximal Ventura County Medical Center, sciatic nerve beneath the piriformis muscles. Severe weakness of these muscles may Ventura, CA 93003, USA. lead to entrapment plexopathy, resulting in diffuse and non-specific pain patterns Correspondence: Kjetil Larsen, CES, Corrective throughout the lumbopelvic complex and lower extremities (LPLE), easily mimicking Exercise Specialist, Training & other diagnoses and is therefore likely to mislead the interpreting clinician. It is a Rehabilitation, Oslo Norway; pathology very similar to that of thoracic outlet syndrome, but for the lower body. This Kjetil@trainingandrehabilitation. two part manuscript series was written in an attempt to demonstrate the existence, com; pathophysiology, diagnostic protocol as well as interventional strategy for LPES, and Tel.: +47 975 45 192 its efficacy. Received: 23 November 2018, Reviewed & Accepted: 28 Key words: Pelvic girdle; Pain, Pelvic girdle; Lumbosacral plexus entrapment syndrome; February 2019 Piriformis syndrome; Nerve entrapment; Double-crush; Pain, Chronic; Fibromyalgia Citation: Larsen K, Chien GCC. Lumbosacral plexus entrapment syndrome. Part one: A common yet little-known cause of chronic pelvic and lower extremity pain. -
ANMC Specialty Clinic Services
Cardiology Dermatology Diabetes Endocrinology Ear, Nose and Throat (ENT) Gastroenterology General Medicine General Surgery HIV/Early Intervention Services Infectious Disease Liver Clinic Neurology Neurosurgery/Comprehensive Pain Management Oncology Ophthalmology Orthopedics Orthopedics – Back and Spine Podiatry Pulmonology Rheumatology Urology Cardiology • Cardiology • Adult transthoracic echocardiography • Ambulatory electrocardiology monitor interpretation • Cardioversion, electrical, elective • Central line placement and venous angiography • ECG interpretation, including signal average ECG • Infusion and management of Gp IIb/IIIa agents and thrombolytic agents and antithrombotic agents • Insertion and management of central venous catheters, pulmonary artery catheters, and arterial lines • Insertion and management of automatic implantable cardiac defibrillators • Insertion of permanent pacemaker, including single/dual chamber and biventricular • Interpretation of results of noninvasive testing relevant to arrhythmia diagnoses and treatment • Hemodynamic monitoring with balloon flotation devices • Non-invasive hemodynamic monitoring • Perform history and physical exam • Pericardiocentesis • Placement of temporary transvenous pacemaker • Pacemaker programming/reprogramming and interrogation • Stress echocardiography (exercise and pharmacologic stress) • Tilt table testing • Transcutaneous external pacemaker placement • Transthoracic 2D echocardiography, Doppler, and color flow Dermatology • Chemical face peels • Cryosurgery • Diagnosis -
The Peripheral Nerves of the Neck, Shoulders and Arms Many Spinal Nerves Form Interlacing Nerve Networks – the Cervical, Brachial, Lumbar and Sacral Nerve Plexuses
The Peripheral Nerves of the Neck, Shoulders and Arms Many spinal nerves form interlacing nerve networks – the cervical, brachial, lumbar and sacral nerve plexuses. The cervical plexus in the neck involves the upper 4 cervical nerves and forms the phrenic nerve which supplies both sensory and motor innervation to the diaphragm which is important for breathing. The brachial plexus in the neck and armpit (axilla) involves C4-T2 and innervates the upper limb (arm and shoulder). These give rise to the axillary nerve, musculocutaneous nerve, median nerve, ulnar nerve and radial nerve (and a few others). The axillary nerve comes out behind the head of humerus to innervate the shoulder joint and the deltoid and teres minor muscles. The musculocutaneous nerve comes down the anterior arm innervates flexion of the forearm and sensory for the laterally forearm. The median nerve comes all the way down the central anterior arm to innervate the forearm flexor muscles and activate pronation of the forearm, flexion of the wrist and fingers and opposition of the thumb. It receives sensory from the forearm skin The ulnar nerve comes down the medial and the lateral palm. side of the arm, goes behind medial condyle of the elbow, down the medial forearm and innervates muscles of the forearm and fingers for wrist and medial finger flexion, adduction and abduction. It receives sensory from the medial side of the hand. The radial nerve is the largest of the nerves off the brachial plexus. It comes down the posterior arm, then wraps around the anterior aide of the lateral epicondyle of the elbow, then splits into a superficial branch and deep branch.