Compressive Mononeuropathies of the Upper Extremity in Chronic Paraplegia
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An Improved Technique for Radial Nerve Conduction Studies
J Neurol Neurosurg Psychiatry: first published as 10.1136/jnnp.30.4.332 on 1 August 1967. Downloaded from J. Neurol. Neurosurg. Psychiat., 1967, 30, 332 An improved technique for radial nerve conduction studies ALLAN W. DOWNIE1 AND THOMAS R. SCOTT From the Division of Neurology, Department of Medicine, School of Medicine, University ofNorth Carolina, Chapel Hill, North Carolina, U.S.A. A technique for recording evoked sensory potentials MATERIALS AND METHOD from the radial nerve has already been reported by us (Downie and Scott, 1964). This technique, The apparatus used was a TECA two-channel electro- myograph. The recording electrodes consisted of a pair although reliable, is time consuming and occasion- of chlorided silver discs 1 cm. in diameter, mounted ally difficult and the amplitude of potentials may be 2 5 cm. apart on a plastic base. The active recording as low as 1 to 2 microvolts. The purpose of this electrode was placed over the largest palpable branch communication is to describe a simpler technique by of the radial nerve as it crossed the tendon of the extensor which potentials of greater amplitude can be pollicis longus. The distal recording electrode was placed obtained. In addition, the segment of nerve tested is over the first dorsal interosseous muscle but not neces- Protected by copyright. one which can be readily identified and biopsied if sarily over the nerve, of which the position in this area so desired without causing unpleasant or disturbing cannot be precisely determined (Fig. 1). An experiment sensory loss to the subject. made to assess the importance of the position of this electrode showed no significant difference in latency to The location of a nerve which is to be tested is peak when it was placed in turn on three points along usually determined by stimulating its motor fibres a line between the tendons of the extensor pollicis and finding the stimulus site from which maximal longus and extensor indicis provided the interelectrode muscle contraction is obtained. -
Intrinsic Hand Muscles of the Japanese Monkey, Macaca Fuscata
Anthropol.Sci. 102(Suppl.), 85-95,1994 Intrinsic Hand Muscles of the Japanese Monkey, Macaca fuscata TOSHIHIKO HOMMA AND TATSUO SAKAI Department of Anatomy, School of Medicine, Juntendo University, Hongo 2-1-1, Bunkyo-ku, Tokyo 113, Japan Received December 24, 1993 •ôGH•ô Abstract•ôGS•ô Anatomy of the intrinsic hand muscles in the Japanese monkeys was studied with an improved method to dissect the muscles and nerves in water after removal of the skeletal framework. The thenar eminence contained four muscles, namely m. abductor pollicis brevis, m. opponens pollicis, m, flexor pollicis brevis, and m. adductor pollicis. The hypothenar eminence contained four muscles, namely m. palmaris brevis, m. abductor digiti minimi, m. flexor digiti minimi brevis, and m. opponens digiti minimi. Majority of the thenar muscles are fused more or less with each other, so that clear separation of these muscles was difficult. The lumbrical muscles arose from the palmar parts of four main tendons of the deep flexor muscle to the second, third, fourth, and fifth digits. The mm, contrahentes arose mainly from a medial tendinous septum attached on the palmar surface to the third metacarpus, and included three muscles destined to the second, fourth and fifth digits. The interossei were found on the radial side of the second, third, fourth and fifth finger as well as on the ulnar side of the second, third and fourth finger. The intrinsic hand muscles in the Japanese monkey received innervation either from the median or the ulnar nerve. Branching pattern of these nerves to the individual muscles was fundamentally similar to those in man except for the fact that the median and the ulnar nerve in the Japanese monkey do not communi cateto make a loop in the thenar muscles. -
A Guide to Transthyretin Amyloidosis
A Guide to Transthyretin Amyloidosis Authored by Teresa Coelho, Bo-Goran Ericzon, Rodney Falk, Donna Grogan, Shu-ichi Ikeda, Mathew Maurer, Violaine Plante-Bordeneuve, Ole Suhr, Pedro Trigo 2016 Edition Edited by Merrill Benson, Mathew Maurer What is amyloidosis? Amyloidosis is a systemic disorder characterized by extra cellular deposition of a protein-derived material, known as amyloid, in multiple organs. Amyloidosis occurs when native or mutant poly- peptides misfold and aggregate as fibrils. The amyloid deposits cause local damage to the cells around which they are deposited leading to a variety of clinical symptoms. There are at least 23 different proteins associated with the amyloidoses. The most well-known type of amyloidosis is associated with a hematological disorder, in which amyloid fibrils are derived from monoclonal immunoglobulin light-chains (AL amyloidosis). This is associated with a clonal plasma cell disorder, closely related to and not uncommonly co-existing with multiple myeloma. Chronic inflammatory conditions such as rheumatoid arthritis or chronic infections such as bronchiectasis are associated with chronically elevated levels of the inflammatory protein, serum amyloid A, which may misfold and cause AA amyloidosis. The hereditary forms of amyloidosis are autosomal dominant diseases characterized by deposition of variant proteins, in dis- tinctive tissues. The most common hereditary form is transthyretin amyloidosis (ATTR) caused by the misfolding of protein monomers derived from the tetrameric protein transthyretin (TTR). Mutations in the gene for TTR frequently re- sult in instability of TTR and subsequent fibril formation. Closely related is wild-type TTR in which the native TTR protein, particu- larly in the elderly, can destabilize and re-aggregate causing non- familial cases of TTR amyloidosis. -
Expert Consensus Recommendations to Improve Diagnosis of ATTR Amyloidosis with Polyneuropathy
Journal of Neurology https://doi.org/10.1007/s00415-019-09688-0 REVIEW Expert consensus recommendations to improve diagnosis of ATTR amyloidosis with polyneuropathy David Adams1 · Yukio Ando2 · João Melo Beirão3 · Teresa Coelho4 · Morie A. Gertz5 · Julian D. Gillmore6 · Philip N. Hawkins6 · Isabelle Lousada7 · Ole B. Suhr8 · Giampaolo Merlini9,10 Received: 10 December 2019 / Revised: 20 December 2019 / Accepted: 23 December 2019 © The Author(s) 2020 Abstract Amyloid transthyretin (ATTR) amyloidosis with polyneuropathy (PN) is a progressive, debilitating, systemic disease wherein transthyretin protein misfolds to form amyloid, which is deposited in the endoneurium. ATTR amyloidosis with PN is the most serious hereditary polyneuropathy of adult onset. It arises from a hereditary mutation in the TTR gene and may involve the heart as well as other organs. It is critical to identify and diagnose the disease earlier because treatments are available to help slow the progression of neuropathy. Early diagnosis is complicated, however, because presentation may vary and family history is not always known. Symptoms may be mistakenly attributed to other diseases such as chronic infammatory demyelinating polyradiculoneuropathy (CIDP), idiopathic axonal polyneuropathy, lumbar spinal stenosis, and, more rarely, diabetic neuropathy and AL amyloidosis. In endemic countries (e.g., Portugal, Japan, Sweden, Brazil), ATTR amyloidosis with PN should be suspected in any patient who has length-dependent small-fber PN with autonomic dysfunction and a family history of ATTR amyloidosis, unexplained weight loss, heart rhythm disorders, vitreous opacities, or renal abnormali- ties. In nonendemic countries, the disease may present as idiopathic rapidly progressive sensory motor axonal neuropathy or atypical CIDP with any of the above symptoms or with bilateral carpal tunnel syndrome, gait disorders, or cardiac hypertro- phy. -
Practical Neurology: Peripheral Neuropathy for the Internist
Practical Neurology: Polyneuropathy for the Non-Neurologist Steven A. Day, MD Providence Neurological Specialties Definitions Foundational Principle: With neurological problems think of LOCALIZATION before SYNDROME Definitions • Neuronopathy – Motor neuronopathy – Sensory neuronopathy • Radiculopathy • Plexopathy • Neuropathy – Mononeuropathy – Polyneuropathy The Netter Collection of Medical Illustrations, Volume 1, Nervous System, 2002 “ROOTS” C4 TRUNKS C5 Dorsal scapular n. C6 TRUNKS C7 Suprascapular n. T1 DIVISIONS Musculocut- aneous n. CCF CORDS 2002 Long thoracic n. TERMINAL NERVES CCF ©2002 Axillary n. Radial n. Median n. Ulnar n. Definitions ‘Neuropathy’ is a diagnosis which specifies the location of pathology, not a symptom Definitions • Axonal = axon loss pathology • Demyelinating = myelin loss pathology Topical Diagnosis in Neurology, 3rd ed. 1998 Topical Diagnosis in Neurology, 3rd ed. 1998 Duss’ Topical Diagnosis in Neurology, 4th ed. 2005 Polyneuropathy Polyneuropathy: Typical Presentation • Insidious onset • Distal (toes, pads of feet) • Gradual progression • Complaints are primarily sensory Polyneuropathy: Key Exam Features • Sensory – Distal gradient of sensory loss • Pin prick or cold • Monofilament • Cotton wisp • Vibration at toes and ankles • Proprioception: toe movements Polyneuropathy: Key Exam Features • Motor – Is there intrinsic foot or hand muscle atrophy? – Weakness pattern • Distal • Proximal and distal • Asymmetric – Able to stand/elevate on toes and heels? Polyneuropathy: Key Exam Features • Reflexes – Distal -
Pronator Syndrome: Clinical and Electrophysiological Features in Seven Cases
J Neurol Neurosurg Psychiatry: first published as 10.1136/jnnp.39.5.461 on 1 May 1976. Downloaded from Journal ofNeurology, Neurosurgery, and Psychiatry, 1976, 39, 461-464 Pronator syndrome: clinical and electrophysiological features in seven cases HAROLD H. MORRIS AND BRUCE H. PETERS From the Department ofNeurology, University of Texas Medical Branch, Galveston, Texas, USA SYNOPSIS The clinical and electrophysiological picture of seven patients with the pronator syndrome is contrasted with other causes ofmedian nerve neuropathy. In general, these patients have tenderness over the pronator teres and weakness of flexor pollicis longus as well as abductor pollicis brevis. Conduction velocity of the median nerve in the proximal forearm is usually slow but the distal latency and sensory nerve action potential at the wrist are normal. Injection of corticosteroids into the pronator teres has produced relief of symptoms in a majority of patients. Protected by copyright. In the majority of isolated median nerve dys- period 101 cases of the carpal tunnel syndrome functions the carpal tunnel syndrome is appropri- and the seven cases of the pronator syndrome ately first suspected. The median nerve can also reported here were identified. Median nerve be entrapped in the forearm giving rise to a conduction velocity determinations were made on similar picture and an erroneous diagnosis. all of these patients. The purpose of this report is to draw full attention to the pronator syndrome and to the REPORT OF CASES features which allow it to be distinguished from Table 1 provides clinical details of seven cases of the median nerve entrapment at other sites. -
Wrist and Hand Examina[On
Wrist and Hand Examinaon Daniel Lueders, MD Assistant Professor Physical Medicine and Rehabilitaon Objecves • Understand the osseous, ligamentous, tendinous, and neural anatomy of the wrist and hand • Outline palpable superficial landmarks in the wrist and hand • Outline evaluaon of and differen.aon between nerves to the wrist and hand • Describe special tes.ng of wrist and hand Wrist Anatomy • Radius • Ulna • Carpal bones Wrist Anatomy • Radius • Ulna • Carpal bones Wrist Anatomy • Radius • Ulna • Carpal bones Wrist Anatomy • Radius • Ulna • Carpal bones Inspec.on • Ecchymosis • Erythema • Deformity • Laceraon Inspec.on • Common Finger Deformies • Swan Neck Deformity • Boutonniere Deformity • Hypertrophic nodules • Heberden’s, Bouchard’s Inspec.on • Swan Neck Deformity • PIP hyperextension, DIP flexion • Pathology is at PIP joint • Insufficiency of volar/palmar plate and suppor.ng structures • Distally, the FDP tendon .ghtens from PIP extension causing secondary DIP flexion • Alternavely, extensor tendon rupture produces similar deformity Inspec.on • Boutonniere Deformity • PIP flexion, DIP hyperextension • Pathology is at PIP joint • Commonly occurs from insufficiency of dorsal and lateral suppor.ng structures at PIP joint • Lateral bands migrate volar/palmar, creang increased flexion moment • Results in PIP “buTon hole” effect dorsally Inspec.on • Nodules • Osteoarthri.c • Hypertrophic changes of OA • PIP - Bouchard’s nodule • DIP - Heberden’s nodule • Rheumatoid Arthri.s • MCP joints affected most • Distal radioulnar joint can also be affected -
The Usefulness of Proximal Radial Motor Conduction in Acute Compressive Radial Neuropathy
JCN Open Access ORIGINAL ARTICLE pISSN 1738-6586 / eISSN 2005-5013 / J Clin Neurol 2015;11(2):178-182 / http://dx.doi.org/10.3988/jcn.2015.11.2.178 The Usefulness of Proximal Radial Motor Conduction in Acute Compressive Radial Neuropathy Kun Hyun Kima b Background and PurposezzThe objective of this study was to determine diagnostic and Kee-Duk Park a prognostic values of proximal radial motor conduction in acute compressive radial neuropathy. Pil-Wook Chung a MethodszzThirty-nine consecutive cases of acute compressive radial neuropathy with radial Heui-Soo Moon conduction studies–including stimulation at Erb’s point–performed within 14 days from a Yong Bum Kim clinical onset were reviewed. The radial conduction data of 39 control subjects were used as a Won Tae Yoon reference data. b Hyung Jun Park ResultszzThirty-one men and eight women (age, 45.2±12.7 years, mean±SD) were enrolled. Bum Chun Suha All 33 patients in whom clinical follow-up data were available experienced complete recov- ery, with a recovery time of 46.8±34.3 days. Partial conduction block was found frequently a Department of Neurology, Kangbuk Samsung Hospital, (17 patients) on radial conduction studies. The decrease in the compound muscle action po- Sungkyunkwan University tential area between the arm and Erb’s point was an independent predictor for recovery time. School of Medicine, Seoul, Korea zzProximal radial motor conduction appears to be a useful method for the early b Conclusions Department of Neurology, detection and prediction of prognosis of acute compressive radial neuropathy. Mokdong Hospital, Ewha Womans University Key Wordszz radial neuropathy, nerve conduction study, conduction block, diagnosis, School of Medicine, Seoul, Korea prognosis. -
A Case of Bickerstaff S Brainstem Encephalitis in Childhood '
View metadata, citation and similar papers at core.ac.uk brought to you by CORE provided by Directory of Open Access Journals Korean Journal of Pediatrics Vol. 53, No. 4, 2010 DOI : 10.3345/kjp.2010.53.4.607 Case report 1)jtj A case of Bickerstaff’s brainstem encephalitis in childhood Ji Youn Kim, M.D., Young Ok Kim, M.D., Young Jun Son, M.D. and Young Jong Woo, M.D. Department of Pediatrics, Chonnam National University Medical School, Gwangju, Korea = Abstract = Bickerstaff's brainstem encephalitis (BBE) is a rare disease diagnosed by specific clinical features such as 'progressive, relatively symmetric external ophthalmoplegia and ataxia by 4 weeks' and 'disturbance of consciousness or hyperreflexia' after the exclusion of other diseases involving the brain stem. Anti-ganglioside antibodies (GM, GD and GQ) in the serum or cerebrospinal fluid (CSF) are sometimes informative for the diagnosis of BBE because of the rarity of positive findings in other diagnositic methods: brain magnetic resonance imaging (MRI), routine CSF examination, motor nerve conduction study, and needle electromyography. We report a rare case of childhood BBE with elevated anti-GM1 antibodies in the serum, who had specific clinical symptoms such as a cranial polyneuropathy presenting as ophthalmoplegia, dysarthria, dysphagia, and facial weakness; progressive motor weakness; altered mental status; and ataxia. However, the brain MRI, routine CSF examination, nerve conduction studies, electromyography, somatosensory evoked potentials, and brainstem auditory evoked potentials were normal. BBE was suspected and the patient was successfully treated with intravenous immunoglobulins. (Korean J Pediatr 2010;53:607-611) Key Words : Encephalitis, Brain stem, Child bulins (IVIG) for the treatment of BBE suggests an auto- Introduction immune etiology5, 6). -
The Muscles That Act on the Upper Limb Fall Into Four Groups
MUSCLES OF THE APPENDICULAR SKELETON UPPER LIMB The muscles that act on the upper limb fall into four groups: those that stabilize the pectoral girdle, those that move the arm, those that move the forearm, and those that move the wrist, hand, and fingers. Muscles Stabilizing Pectoral Girdle (Marieb / Hoehn – Chapter 10; Pgs. 346 – 349; Figure 1) MUSCLE: ORIGIN: INSERTION: INNERVATION: ACTION: ANTERIOR THORAX: anterior surface coracoid process protracts & depresses Pectoralis minor* pectoral nerves of ribs 3 – 5 of scapula scapula medial border rotates scapula Serratus anterior* ribs 1 – 8 long thoracic nerve of scapula laterally inferior surface stabilizes / depresses Subclavius* rib 1 --------------- of clavicle pectoral girdle POSTERIOR THORAX: occipital bone / acromion / spine of stabilizes / elevates / accessory nerve Trapezius* spinous processes scapula; lateral third retracts / rotates (cranial nerve XI) of C7 – T12 of clavicle scapula transverse processes upper medial border elevates / adducts Levator scapulae* dorsal scapular nerve of C1 – C4 of scapula scapula Rhomboids* spinous processes medial border adducts / rotates dorsal scapular nerve (major / minor) of C7 – T5 of scapula scapula * Need to be familiar with on both ADAM and the human cadaver Figure 1: Muscles stabilizing pectoral girdle, posterior and anterior views 2 BI 334 – Advanced Human Anatomy and Physiology Western Oregon University Muscles Moving Arm (Marieb / Hoehn – Chapter 10; Pgs. 350 – 352; Figure 2) MUSCLE: ORIGIN: INSERTION: INNERVATION: ACTION: intertubercular -
Peripheral Polyneuropathy in Patients Receiving Long-Term Statin Therapy
552 Turk Kardiyol Dern Ars 2019;47(7):552-553 doi: 10.5543/tkda.2019.52735 Invited Editorial / Davetli Editöryal Yorum Peripheral polyneuropathy in patients receiving long-term statin therapy Uzun dönem statin kullanan hastalarda periferik polinöropati gelişimi Öner Özdoğan, M.D. Department of Cardiology, Tepecik Training and Research Hospital, İzmir, Turkey Although drug-induced neuropathies (DIN) are not an enzyme which could Abbreviation: very common, they are one of the main reasons of pe- alter the neurons’ energy DIN Drug-induced neuropathies ripheral neuropathies.[1] DIN cause to sensory, motor, utilization.[6] On the con- ENMG Electroneuromyography and autonomic dysfunctions depending on the type of SAMs Statin-associated muscle trary; some animal stu- symptoms the peripheral nerve involvement. As significant re- dies have reported that covery could be observed after discontinuation of the statins provided a neuroprotective effect against pe- causal agent drug, early diagnosis is important. How- ripheral nerve injury.[7] In a recent Danish case-control ever, symptoms of DIN are usually seen after months study, use of statins in 370 cases, was not associated [2] or years of exposure. Therefore, defining the causal with an elevated risk of polyneuropathy. Similarly, no relationship between the drugs and long term side ef- association was observed between polyneuropathy fects like drug-induced peripheral neuropathies is not risk and long-term high-intensity statin.[8] easy always, and commonly missed. Electrodiagnos- tic tests are the most important methods to confirm In this issue of the Archives of Turkish Society tthe peripheral neuropathy.[3] We classify the type of of Cardiology, Ozdemir et al. -
Posterior Interosseous Neuropathy Supinator Syndrome Vs Fascicular Radial Neuropathy
Posterior interosseous neuropathy Supinator syndrome vs fascicular radial neuropathy Philipp Bäumer, MD ABSTRACT Henrich Kele, MD Objective: To investigate the spatial pattern of lesion dispersion in posterior interosseous neurop- Annie Xia, BSc athy syndrome (PINS) by high-resolution magnetic resonance neurography. Markus Weiler, MD Methods: This prospective study was approved by the local ethics committee and written Daniel Schwarz, MD informed consent was obtained from all patients. In 19 patients with PINS and 20 healthy con- Martin Bendszus, MD trols, a standardized magnetic resonance neurography protocol at 3-tesla was performed with Mirko Pham, MD coverage of the upper arm and elbow (T2-weighted fat-saturated: echo time/repetition time 52/7,020 milliseconds, in-plane resolution 0.27 3 0.27 mm2). Lesion classification of the radial nerve trunk and its deep branch (which becomes the posterior interosseous nerve) was performed Correspondence to Dr. Bäumer: by visual rating and additional quantitative analysis of normalized T2 signal of radial nerve voxels. [email protected] Results: Of 19 patients with PINS, only 3 (16%) had a focal neuropathy at the entry of the radial nerve deep branch into the supinator muscle at elbow/forearm level. The other 16 (84%) had proximal radial nerve lesions at the upper arm level with a predominant lesion focus 8.3 6 4.6 cm proximal to the humeroradial joint. Most of these lesions (75%) followed a specific somato- topic pattern, involving only those fascicles that would form the posterior interosseous nerve more distally. Conclusions: PINS is not necessarily caused by focal compression at the supinator muscle but is instead frequently a consequence of partial fascicular lesions of the radial nerve trunk at the upper arm level.