The Reemergence of Acute Flaccid Myelitis
Total Page:16
File Type:pdf, Size:1020Kb
Load more
Recommended publications
-
Central Pain in the Face and Head
P1: KWW/KKL P2: KWW/HCN QC: KWW/FLX T1: KWW GRBT050-128 Olesen- 2057G GRBT050-Olesen-v6.cls August 17, 2005 2:10 ••Chapter 128 ◗ Central Pain in the Face and Head J¨orgen Boivie and Kenneth L. Casey CENTRAL PAIN IN THE FACE AND HEAD Anesthesia dolorosa denotes pain in a region with de- creased sensibility after lesions in the CNS or peripheral International Headache Society (IHS) code and diag- nervous system (PNS). The term deafferentation pain is nosis: used for similar conditions, but it is more commonly used in patients with lesions of spinal nerves. 13.18.1 Central causes of facial pain 13.18.1 Anesthesia dolorosa (+ code to specify cause) 13.18.2 Central poststroke pain EPIDEMIOLOGY 13.18.3 Facial pain attributed to multiple sclerosis 13.18.4 Persistent idiopathic facial pain The prevalence of central pain varies depending on the un- 13.18.5 Burning mouth syndrome derlying disorder (Tables 128-1 and 128-2) (7,29). In the ab- 13.19 Other centrally mediated facial pain (+ code to sence of large scale epidemiologic studies, only estimates specify etiology) of central pain prevalence can be quoted. In the only prospective epidemiologic study of central Note that diagnosis with IHS codes 13.18.1, 13.18.4, and pain, 191 patients with central poststroke pain (CPSP) 13.18.5 may have peripheral causes. were followed for 12 months after stroke onset (1). Sixteen World Health Organization (WHO) code and diagnosis: (8.4%) developed central pain, an unexpectedly high inci- G 44.810 or G44.847. -
Acute Flaccid Myelitis a Rare Entity. Hina Yusuf Shifa International Hospital
Pakistan Journal of Neurological Sciences (PJNS) Volume 14 | Issue 2 Article 3 6-2019 Is it really transverse myelitis? Acute flaccid Myelitis a rare entity. Hina Yusuf Shifa International Hospital. Islamabad, Pakistan Arsalan Ahmad Shifa International Hospital. Islamabad, Pakistan. Ejaz Ahmed Khan Shifa International Hospital, Islamabad Follow this and additional works at: https://ecommons.aku.edu/pjns Part of the Neurology Commons Recommended Citation Yusuf, Hina; Ahmad, Arsalan; and Khan, Ejaz Ahmed (2019) "Is it really transverse myelitis? Acute flaccid Myelitis a rare entity.," Pakistan Journal of Neurological Sciences (PJNS): Vol. 14 : Iss. 2 , Article 3. Available at: https://ecommons.aku.edu/pjns/vol14/iss2/3 CASE REPORT remained bed bound, fully dependant on her family for months to 15 years. The illness usually begins with a REFERENCES IS IT REALLY TRANSVERSE MYELITIS? ACUTE FLACCID all activities of daily life. As before there were no prodromal phase of febrile illness with flu like 4. Sejvar JJ, Lopez AS, Cortese MM, Leshem E, Pastula MYELITIS A RARE ENTITY bladder or bowel complaints. She continued to have symptoms, usually followed by headache, neck . Pastula DM, Aliabadi N, Haynes AK, Messacar K, DM, Miller L, Glaser C, Kambhampati A, Shioda K, flaccid paralysis with marked muscle wasting and stiffness and backache. The patients then develop Schreiner T, Maloney J, Dominguez SR, Davizon Aliabadi N, Fischer M. Acute flaccid myelitis in the occasional fasciculations. Power had improved to 2/5 rapidly progressive lower motor neuron type limb ES, Leshem E, Fischer M, Nix WA. Acute neurologic United States, August–December 2014: results of 1 2 3 Dr Hina Yusuf , Prof Arsalan Ahmad , Prof Ejaz Ahmed Khan in both upper limbs. -
Cervical Myelopathy • Pragmatic Review
DIAGNOSIS AND INDICATIONS FOR SURGERY Cervical Spondylitic Myelopathy Timothy A. Garvey, MD Twin Cities Spine Center Minneapolis, MN Cervical Myelopathy • Pragmatic review • Differential diagnosis • History and physical exam • Reality check – clinical cases last few months • Every-day clinical decisions Cervical Myelopathy • Degenerative • Cervical spondylosis, stenosis, OPLL • Trauma • SCI, fracture • Tumor • Neoplasms • Autoimmune • MS, ALS, SLE, etc. • Congenital • Syrinx, Chiari, Down’s Cervical Myelopathy • Infection • Viral: HIV, polio, herpes • Bacterial: Syphilis, epidural abscess • Arthritis • RA, SLE. Sjogren • Vascular • Trauma, AVM, Anklosing spondylitis • Metabolic • Vitamin, liver, gastric bypass, Hepatitis C • Toxins • Methalene blue, anesthetics • Misc. • Radiation, baro trauma, electrical injury Myelopathy • Generic spinal cord dysfunction • Classification systems • Nurick, Ranawat, JOA • Nice review • CSRS 2005, Chapter 15 – Lapsiwala & Trost Cervical Myelopathy • Symptoms • Gait disturbance Ataxia • Weakness, hand function • Sensory – numbness and tingling • Bladder - urgency Cervical Myelopathy • Signs • Reflexes – hyper-reflexia, clonus • Pathologic – Hoffman’s, Babinski • Motor – weakness • Sensory – variable • Ataxia – unsteady gait • Provocative – Lhrmitte’s Pathophysiology/CSM • Cord compression with distortion • Ischemia – anterior spinal flow • Axoplasmic flow diminution • Demyelinization of the white matter in both ascending and descending traits L.F. • 48 year-old female w/work injury • “cc” – left leg dysfunction – Mild urinary frequency – More weakness than pain • PE – Mild weakness, multiple groups – No UMN L.F. 08/06 L4-5 L2-3 L.F. 09/07 L.F. 1/07 L.F. 7/07 Asymptomatic MRI • 100 patients • Disc Protrusion – 20% of 45 – 54 year olds – 57% of > 64 year olds • Cord Impingement – 16% < 64 – 26% > 64 • Cord Compression – 7 of 100 Asymptomatic Degenerative Disk Disease and Spondylosis of the Cervical Spine: MR Imaging. -
Caspr2 Antibodies in Patients with Thymomas
View metadata, citation and similar papers at core.ac.uk brought to you by CORE provided by Elsevier - Publisher Connector MALIGNANCIES OF THE THYMUS Caspr2 Antibodies in Patients with Thymomas Angela Vincent, FRCPath,* and Sarosh R. Irani, MA* neuromuscular junction. Neuromyotonia (NMT) is due to Abstract: Myasthenia gravis is the best known autoimmune disease motor nerve hyperexcitability that leads to muscle fascicula- associated with thymomas, but other conditions can be found in tions and cramps. A proportion of patients have antibodies patients with thymic tumors, including some that affect the central that appear to be directed against brain tissue-derived volt- nervous system (CNS). We have become particularly interested in age-gated potassium channels (VGKCs) that control the ax- patients who have acquired neuromyotonia, the rare Morvan disease, onal membrane potential.4,5 VGKC antibody titers are rela- or limbic encephalitis. Neuromyotonia mainly involves the periph- tively low in NMT. eral nerves, Morvan disease affects both the peripheral nervous Morvan disease is a rare condition first described in system and CNS, and limbic encephalitis is specific to the CNS. 1876 but until recently hardly mentioned outside the French Many of these patients have voltage-gated potassium channel auto- literature.6 The patients exhibit NMT plus autonomic distur- antibodies. All three conditions can be associated with thymomas bance (such as excessive sweating, constipation, and cardiac and may respond to surgical removal of the underlying tumor -
Syringomyelia in Cervical Spondylosis: a Rare Sequel H
THIEME Editorial 1 Editorial Syringomyelia in Cervical Spondylosis: A Rare Sequel H. S. Bhatoe1 1 Department of Neurosciences, Max Super Specialty Hospital, Patparganj, New Delhi, India Indian J Neurosurg 2016;5:1–2. Neurological involvement in cervical spondylosis usually the buckled hypertrophic ligament flavum compresses the implies radiculopathy or myelopathy. Cervical spondylotic cord. Ischemia due to compromise of microcirculation and myelopathy is the commonest cause of myelopathy in the venous congestion, leading to focal demyelination.3 geriatric age group,1 and often an accompaniment in adult Syringomyelia is an extremely rare sequel of chronic cervical patients manifesting central cord syndrome and spinal cord cord compression due to spondylotic process, and manifests as injury without radiographic abnormality. Myelopathy is the accelerated myelopathy (►Fig. 1). Pathogenesis of result of three factors that often overlap: mechanical factors, syringomyelia is uncertain. Al-Mefty et al4 postulated dynamic-repeated microtrauma, and ischemia of spinal cord occurrence of myelomalacia due to chronic compression of microcirculation.2 Age-related mechanical changes include the cord, followed by phagocytosis, leading to a formation of hypertrophy of the ligamentum flavum, formation of the cavity that extends further. However, Kimura et al5 osteophytic bars, degenerative disc prolapse, all of them disagreed with this hypothesis, and postulated that following contributing to a narrowing of the spinal canal. Degenerative compression of the cord, there is slosh effect cranially and kyphosis and subluxation often aggravates the existing caudally, leading to an extension of the syrinx. It is thus likely compressiononthespinalcord.Flexion–extension that focal cord cavitation due to compression and ischemia movements of the spinal cord places additional, dynamic occurs due to periventricular fluid egress into the cord, the stretch on the cord that is compressed. -
Neurosyphilis Presenting with Myelitis-Case Series and Literature Review
Neurosyphilis presenting with myelitis-Case series and literature review Yali Wu Capital Medical University Aliated Beijing Ditan Hospital https://orcid.org/0000-0002-9737-6439 Wenqing Wu ( [email protected] ) https://orcid.org/0000-0001-7428-5529 Case report Keywords: Syphilis, Neurosyphilis, Spinal cord, Magnetic resonance imaging Posted Date: April 5th, 2019 DOI: https://doi.org/10.21203/rs.2.1849/v1 License: This work is licensed under a Creative Commons Attribution 4.0 International License. Read Full License Version of Record: A version of this preprint was published at Journal of Infection and Chemotherapy on February 1st, 2020. See the published version at https://doi.org/10.1016/j.jiac.2019.09.007. Page 1/9 Abstract Background Neurosyphilis is a great imitator because of its various clinical symptoms. Syphilitic myelitis is extremely rare manifestation of neurosyphilis and often misdiagnosed. However, a small amount of literature in the past described its clinical manifestations and imaging features, and there was no relevant data on the prognosis, especially the long-term prognosis. In this paper, 4 syphilis myelitis patients admitted to our hospital between July 2012 and July 2017 were retrospectively reviewed. In the 4 patients, 2 were females, and 2 were males. We present our experiences with syphilitic myelitis, discuss the characteristics, treatment and prognosis. Case presentation The diagnosis criteria were applied: (1) diagnosis of myelitis established by two experienced neurologist based on symptoms and longitudinally extensive transverse myelitis (LETM) at the cervical and thoracic levels mimicked neuromyelitis optic (NMO) on magnetic resonance imaging (MRI) ; (2) Neurosyphilis (NS) was diagnosed by positive treponema pallidum particle assay (TPPA) and toluidine red untreated serum test (TRUST) in the serum and CSF; (3) negative human immunodeciency virus (HIV). -
Autoimmune Neurological Disorders - Does the Age Matter?
1 Autoimmune neurological disorders - does the age matter? Yael Hacohen1,2 and Angela Vincent3 1. Department of Paediatric Neurology, Great Ormond Street Hospital for Children, London, 2. Department of Neuroinflammation, Queen Square MS Centre, UCL Institute of Neurology, London. 3. Nuffield Department of Clinical Neurosciences, John Radcliffe Hospital, Oxford. Antibodies binding to central nervous system (CNS) channels, receptors and other synaptic or glial proteins are now recognised as a likely cause of neurological disorders in both adults and children (see Table). Autoimmune encephalopathies are characterized variously by impaired alertness, amnesia, seizures, movement disorders, psychiatric features or autonomic instability, but without focal neurological deficits. The neuronal cell-surface antigens are essential to cellular function or neurotransmission and are generally expressed throughout the nervous system1. Autoimmune forms of demyelinating disorders, by contrast, can present as optic neuritis, transverse myelitis or a range of CNS presentations reflecting the site of the lesions. The glial (myelin or astrocyte) cell-surface antigens are widely expressed throughout the CNS. All these patients frequently respond well to immunotherapies, and in some cases the disorders are monophasic and do not require long-term immunosuppression2. By contrast, the typical paraneoplastic antibodies are generated against tumour antigens that are shared with the nervous system, and are usually associated with T cell-mediated pathogenic mechanisms; the antibodies represent an epiphenomenon of the disease but can be useful biomarkers for the existence of the appropriate tumour. Unfortunately, patients with the intracellular antibodies often progress relentlessly and do not respond to immunotherapies3. The strongest levels of evidence linking identified cell surface antibodies to the pathology of specific disorders are found with AQP4 antibody in neuromyelitis optica spectrum disorder and NMDAR antibody in NMDAR-antibody encephalitis. -
Transverse Myelitis After Diphtheria, Tetanus, and Polio Immunisation
1450 BRITISH MEDICAL JOURNAL 4 JUNE 1977 The patient recovered completely and was treated with co-trimoxazole to the umbilicus. Sensation to pinprick was absent up to the level of T4 5; 3 tablets twice daily for a further six months. At six months x-ray examina- at this level the child cried and tried to push the pin away. The power, tone, tion showed sclerosis of the right sacroiliac joint and irregularities of the and reflexes in her arms were normal and the cranial nervcs were normal. joint margins. All other systems were normal. Br Med J: first published as 10.1136/bmj.1.6074.1450 on 4 June 1977. Downloaded from Initial investigations showed a white cell count of 16-2 109 1(16 200 mm:, with 58 °, lymphocytes and 34 ",, mature neutrophils. Her cerebrospinal Comment fluid (CSF) was clear and tunder pressure of 160 mm of watcr. It contained four polymorphs, tw!o lymphocytes, two red cells, and a protein concentra- This case illustrates the facts, well-recognised by microbiologists, tion of 0-3 g 1 (30 mg 100 ml). A myelogram gave a normal result. Virology that most salmonella serotypes may invade the blood stream and that of the CSF and throat showed nothing abnormal. Poliovirus type 2 was systemic disease need not be preceded by gastrointestinal isolated from the stools. symptoms,' Shc was started on dexamethasone 1 mg four times daily for four days, nor need the patient have an overt susceptibility to bacteraemia. followed by prednisolone 5 mg three times daily continued for a six xeek Acute suppurative arthritis or osteomyelitis is usually due to Staphy- period. -
ICD9 & ICD10 Neuromuscular Codes
ICD-9-CM and ICD-10-CM NEUROMUSCULAR DIAGNOSIS CODES ICD-9-CM ICD-10-CM Focal Neuropathy Mononeuropathy G56.00 Carpal tunnel syndrome, unspecified Carpal tunnel syndrome 354.00 G56.00 upper limb Other lesions of median nerve, Other median nerve lesion 354.10 G56.10 unspecified upper limb Lesion of ulnar nerve, unspecified Lesion of ulnar nerve 354.20 G56.20 upper limb Lesion of radial nerve, unspecified Lesion of radial nerve 354.30 G56.30 upper limb Lesion of sciatic nerve, unspecified Sciatic nerve lesion (Piriformis syndrome) 355.00 G57.00 lower limb Meralgia paresthetica, unspecified Meralgia paresthetica 355.10 G57.10 lower limb Lesion of lateral popiteal nerve, Peroneal nerve (lesion of lateral popiteal nerve) 355.30 G57.30 unspecified lower limb Tarsal tunnel syndrome, unspecified Tarsal tunnel syndrome 355.50 G57.50 lower limb Plexus Brachial plexus lesion 353.00 Brachial plexus disorders G54.0 Brachial neuralgia (or radiculitis NOS) 723.40 Radiculopathy, cervical region M54.12 Radiculopathy, cervicothoracic region M54.13 Thoracic outlet syndrome (Thoracic root Thoracic root disorders, not elsewhere 353.00 G54.3 lesions, not elsewhere classified) classified Lumbosacral plexus lesion 353.10 Lumbosacral plexus disorders G54.1 Neuralgic amyotrophy 353.50 Neuralgic amyotrophy G54.5 Root Cervical radiculopathy (Intervertebral disc Cervical disc disorder with myelopathy, 722.71 M50.00 disorder with myelopathy, cervical region) unspecified cervical region Lumbosacral root lesions (Degeneration of Other intervertebral disc degeneration, -
Transverse Myelitis Interagency Collaboration
SHNIC Specialized Health Needs Factsheet: Transverse Myelitis Interagency Collaboration What is it? Transverse Myelitis is a neurological disorder caused by inflammation of the spinal cord. A child will experience weakness, pain, sensory and autonomic dysfunction. Auto- nomic, involuntary activities such as breathing, digestion, heartbeat and reflexes can be affected. Symptoms can ap- pear suddenly within hours or progress over a span of sev- eral weeks. Approximately 25% of cases are children. A peak in incidence occurs between ages of 10 and 19 and females are at higher risk than men. During an inflammato- ry response the myelin, or protective fatty coating on nerve cells, is damaged or destroyed. TM can also be the first symptom to diagnose Multiple Sclerosis. What causes it? Researchers believe it is the body’s immune response, not the infection itself, that causes the inflammatory response. This indicates an auto-immune reaction, where the body attacks it’s own tissue rather than the infection, is responsible. Research has made connections to the damage of spinal nerves following a viral or bacterial infection, especially those associated with a rash. According to the National Institute of Neurologic Disorders and Stroke, infectious agents sus- pected of causing TM include Varicella zoster (the virus that causes chickenpox and shingles), Herpes simplex, Cytomegalovirus, Epstein-Barr, Influenza, Echovirus, Human immunodefi- ciency virus (HIV), Hepatitis A, and Rubella. In some cases, bacterial infections like a middle ear infection and bacterial pneumonia have also been linked. What are the symptoms? Symptoms can start slowly and progressively worsen over hours or days. Damage depends on the affected area of the spinal cord. -
Acute Flaccid Myelitis (AFM) Surveillance Guidance for County Health Departments (Chds) Th Version 6 | August 5 , 2020
Acute Flaccid Myelitis (AFM) Surveillance Guidance for County Health Departments (CHDs) Version 6 | August 5th, 2020 Surveillance and Investigation When counties receive a report of possible AFM, we ask that you do the following: 1. Ask the provider to complete the FL-specific patient summary form and submit medical records (including infectious disease and neurology consult notes and MRI report), and MRI images (MRI images can come on a CD or flash drive). Ask the provider to mail MRI images on a CD/flash drive to the AFM Epidemiologist: Jenna Webb, 4052 Bald Cypress Way, Bin A-12 Tallahassee, FL 32399–1720 2. Create a case in Merlin using the Acute Flaccid Myelitis disease code (04910). Attach the MRI report, medical records, and patient summary form (select “report form” document type), then submit. The state will complete the rest of the data entry. 3. Notify your regional epidemiologist and laboratory liaison and the AFM Epidemiologist, Jenna Webb, of the AFM Person Under Investigation (PUI). 4. Ask the provider to work with their laboratory to submit available specimens to the Bureau of Public Health Laboratories (BPHL) along with a completed BPHL lab submission form with “AFM PUI” in the comments section. No specific test orders are necessary. Although shipping frozen specimens is ideal, refrigerated specimens are acceptable if shipped to BPHL overnight in a cooler box with frozen gel ice. Find the here: CDC Specimen Collection Instructions 5. BPHL will conduct enterovirus (including Enterovirus-D68), influenza, and respiratory virus panel PCR testing and West Nile virus IgM testing. 6. Providers should be made aware that laboratory results via BPHL or CDC are not intended for clinical diagnosis or clinical decision making and may not get reported back to Bureau of Epidemiology (BOE) or the submitting provider. -
Inflammation of the Central Nervous System- Encephalitis, Myelitis, and Meningitis
Inflammation of the Central Nervous System- Encephalitis, Myelitis, and Meningitis Stacy Dillard, DVM, Diplomate ACVIM (Neurology) Inflammation of the central nervous system is a very common condition seen in veterinary neurology. The area in which the inflammation predominates indicates which of the clinical syndromes we use to name the disease. Inflammation involving the brain is called encephalitis, of the spinal cord is called myelitis and of the meninges is called meningitis. It is common to have more than one area of the central nervous system affected and therefore combinations of the names are often used such as meningoencephalomyelitis or meningoencephalitis. Encephalitis is the most common area of the central nervous system to be affected and will be used as the general term in this article. Etiology There are two main classes of encephalitis: infectious and idiopathic. Infectious etiologies include viruses, fungi, bacteria, protozoa, tick borne diseases and even algae. True infectious encephalitis is much less common in the dog than in other species including humans; however diagnosis is critical for proper targeted therapy. Idiopathic encephalitis means that an infectious etiology has not been found and encompasses a wide range of syndromes appreciated in the canine patient. Many idiopathic encephalitidies are thought to be immune-mediated and respond well to immune-suppression. Other idiopathic encephalitis, such as necrotizing encephalitis found in young toy breed dogs, do not appear to respond as well to immuno- suppression and therefore may represent another form of the disease. Idiopathic encephalitis is much more common in the dog than infectious encephalitis; however, definitive diagnosis is critical as treatment is markedly different between the two categories of disease.