Ice Pack Test for Myasthenia Gravis LETTER to the EDITORS

Total Page:16

File Type:pdf, Size:1020Kb

Ice Pack Test for Myasthenia Gravis LETTER to the EDITORS View metadata, citation and similar papers at core.ac.uk brought to you by CORE provided by RERO DOC Digital Library J Neurol (2003) 250:883–884 DOI 10.1007/s00415-003-1121-1 LETTER TO THE EDITORS Adam Czaplinski countries. According to previous we cooled the more affected eye. Andreas J. Steck publications local cooling improves The ice pack was then removed af- Peter Fuhr neuromuscular transmission, ter 2 minutes. After 10 minutes, whereas warming has the opposite three i. v. injections, one containing effect [1]. However, the precise 10 mg edrophonium and two Ice pack test for mechanism of this effect is unclear. placebo, were administered in a myasthenia gravis Reduction or inhibition of the ac- double blinded fashion by a nurse. tivity of acetylcholinesterase by Photographs were taken immedi- A simple, noninvasive and safe lowering temperature is a possible ately after cooling or 1 minute after diagnostic method mechanism [8]. The purpose of the injection. All pictures were re- present article is to be a reminder viewed by a blinded observer. Out- Received: 24 January 2003 of an alternate method to tensilon come measure was the effect of ice Accepted: 27 February 2003 testing that is simple and safe but or edrophonium on ptosis. seems to have fallen into oblivion Results: Five subjects improved in the neurological literature. with the ice test; however, in one of Sirs: Intravenous injection of the Design/Methods: Five patients them the edrophonium test was acetylcholinesterase inhibitor edro- with ptosis from previously undi- negative. All subjects with positive phonium (tensilon) is commonly agnosed myasthenia gravis and five response to orbital cooling were used in the diagnosis of myasthe- with non-myasthenic ptosis were subsequently shown to have myas- nia gravis (MG), because of rapid studied with the use of tensilon thenia gravis by other tests (ele- onset and short duration of its ef- testing, orbital cooling, and other vated titers of anti-acetylcholine fects. The estimated sensitivity of tests for MG such as repetitive receptor antibody and compound tensilon testing in myasthenia nerve stimulation and determina- muscle action potential (CMAP) gravis is high; however, false-nega- tion of antiacetylcholine receptor amplitude decrement to repetitive tive responses have been reported. antibody (AchR-ab) levels. Each stimulation greater than 20%). Pa- Tensilon, however, may produce se- patient was photographed before tients with non-myasthenic ptosis rious side effects, including signifi- ice or tensilon testing. In the ice (negative anti-acetylcholine recep- cant bradycardia, loss of conscious- test, the patient was asked to hold tor antibody titer and no decre- ness and death [4]. Consequently an ice pack (ice cube wrapped in a mental response in repetitive nerve its use has been restricted in surgical glove) over the closed eye stimulation tests) did not improve Switzerland and in other European with ptosis. If ptosis was bilateral, in either ice or edrophonium test. Fig. 1 (A) before testing; (B) after ice-test (ice application to the right eyelid); (C) after edrophonium test a) b) JON 1121 c) 884 No patient had a false-positive or with negative edrophonium test References paradoxical response to the ice test. were found in our study and also in No side effects, except for moderate the studies of Sethi et al. and Gol- 1. Borenstein S, Desmedt JE (1975) Local local discomfort in the ice test, nik et al. However, both ice and cooling in myasthenia. Improvement of neuromuscular failure. Arch Neurol 32: were observed. edrophonium tests yield also false 152–157 Discussion: According to our negative responses. According to 2. Ellis FD, Hoyt CS, Ellis FJ, Jeffery AR, limited data, the ice test seems to previous studies improvement in Sondhi N (2000) Extraocular muscle re- be relatively sensitive for the diag- eyelid elevation after the ice test is sponses to orbital cooling (ice test) for ocular myasthenia gravis diagnosis. J nosis of myasthenia gravis in pa- in part caused by rest [7]. A com- AAPOS 4:271–281 tients with ocular symptoms: in parison of both ice and sleep test in 3. Golnik KC, Pena R, Lee AG, Eggenberger our group all patients subsequently a group of 10 subjects with myas- ER (1999) An ice test for the diagnosis shown to have myasthenia gravis thenic ptosis and 15 with non- of myasthenia gravis. Ophthalmology 106:1282–1286 by other tests improved in ice test. myasthenic ptosis in a randomised 4. Ing EB, Ing SY,Ramocki JA (2000) The These results are in agreement with trial was performed by Kubis et al. complication rate of edrophonium test- the previously published studies. [5]. Whereas there was no improve- ing for suspected myasthenia gravis. Golnik et al. observed improvement ment in ptosis in non-myasthenic Can J Ophthalmol 35:141–144 in myasthenic ptosis after the ice subjects, in myasthenic patients the 5. Kubis KC, Danesh-Meyer HV,Savino PJ, Sergott RC (2000) The ice test versus test in 16 of 20 patients with myas- median improvement of ptosis rest test in myasthenia gravis. Ophthal- thenia gravis [3], Sethi et al. in 8 of with the rest test was 2 mm and mology 107:1195–1198 10 patients [8] and Lertchavanakul with the ice test was 4,5 mm. This 6. Lerchavanakul A, Gamnerdsiri P,Hirun- in 19 of 20 patients [6]. Although difference between the rest (sleep) wiwatkul P (2001) Ice test for ocular myasthenia gravis. J Med Assoc Thai 84 the sensitivity of the ice test was test and ice tests was significant (Suppl 1):S31–S36 not 100%, as has been also re- (p < 0.001). Both our results and re- 7. Movaghar M, Slavin ML (2000) Effect of ported [2, 5] these results support view of the literature confirm that local heat versus ice on blepharoptosis the validity of the ice test in the di- the ice test seems to be a reliable, resulting from ocular myasthenia. Ophthalmology 107:2209–2214 agnosis of MG. Moreover, the safe, simple, sensitive and specific 8. Sethi KD, Rivner MH, Swift TR (1987) specificity of the ice test appears to diagnostic method for the diagno- Ice pack test for myasthenia gravis. be very high. Patients with non- sis of myasthenia gravis in patients Neurology 37:1383–1385 myasthenic ptosis do not improve with ocular ptosis. However, the in the ice test [2, 3, 5, 6, 8]. The ice most important disadvantage of A. Czaplinski, MD (౧) · A. J. Steck · P.Fuhr test may also be useful in the diag- this method in comparison with Dept. of Neurology nosis of myasthenia gravis, even in the tensilon test is the inability to University Hospital Basel patients in whom edrophonium conduct this test in a double-blind Petersgraben 4 testing is negative. Patients with a fashion. 4031 Basel, Switzerland Tel.: +41-61/265-2525 positive response in the ice test but Fax: +41-61/265-4100 E-Mail: [email protected].
Recommended publications
  • Neuromyelitis Optica in Patients with Myasthenia Gravis Who Underwent Thymectomy
    ORIGINAL CONTRIBUTION Neuromyelitis Optica in Patients With Myasthenia Gravis Who Underwent Thymectomy Ilya Kister, MD; Sandeep Gulati, MD; Cavit Boz, MD; Roberto Bergamaschi, MD; Guiseppe Piccolo, MD; Joel Oger, MD; Michael L. Swerdlow, MD Background: Myasthenia gravis (MG) and neuromy- Patients: Four patients with MG who underwent elitis optica (NMO, also known as Devic disease) are rare thymectomy. autoimmune disorders, with upper-limit prevalence es- timates in the general population of 15 per 100 000 and Interventions: None. 5 per 100 000, respectively. To our knowledge, an asso- ciation between these diseases has not been previously Results: The prevalence of MG within the published co- reported. hort of patients with NMO is more than 150 times higher than that in the general population. Objectives: To describe 4 patients with MG who de- Conclusion: Dysregulation of B-cell autoimmunity in my- veloped NMO after thymectomy and to analyze possible asthenia, possibly exacerbated by loss of control over au- causes of apparent increased prevalence of NMO among toreactive cells as a result of thymectomy, may predis- patients with MG. pose patients to the development of NMO. Design: Case series. Arch Neurol. 2006;63:851-856 EUROMYELITIS OPTICA REPORT OF CASES (NMO) is characterized by 1 or more attacks of CASE 1 optic neuritis (ON) and myelitis. It can be dif- An African American woman with mild Nferentiated from multiple sclerosis (MS) asthma, distant history of smoking and with the aid of magnetic resonance imag- cocaine snorting, and family history of ing (MRI),1-3 cerebrospinal fluid anal- MS in her mother developed symptoms ysis4-8 and NMO-IgG antibody.9 The of ocular myasthenia at age 38 years.
    [Show full text]
  • Targeting the Rare Co-Occurrence of Myasthenia Gravis and Graves’ Disease with Radioactive Iodine Therapy
    ID: 21-0046 -21-0046 A E S Arcellana and others Myasthenia gravis, Graves’ ID: 21-0046; July 2021 disease association DOI: 10.1530/EDM-21-0046 Dual attack: targeting the rare co-occurrence of myasthenia gravis and Graves’ disease with radioactive iodine therapy Correspondence Anna Elvira S Arcellana 1, Karen Joy B Adiao2 and Myrna Buenaluz-Sedurante1 should be addressed to A E S Arcellana 1Division of Endocrinology, Diabetes and Metabolism, Department of Medicine and 2Department of Neurosciences, Email University of the Philippines-Manila, Philippine General Hospital, Manila, Philippines [email protected] Summary Occasionally, autoimmune disorders can come in twos. This double trouble creates unique challenges. Myasthenia gravis co-existing with autoimmune thyroid disease occurs in only about 0.14–0.2% of cases. The patient is a 27-year- old man with a 2-month history of bilateral ptosis, diplopia, with episodes of easy fatigability, palpitations, and heat intolerance. On physical exam, the patient had an enlarged thyroid gland. Myasthenia gravis was established based on the presence of ptosis with weakness of the intraocular muscles, abnormal fatigability, and a repetitive nerve stimulation studyindicatedneuromuscularjunctiondisease.Episodesoffluctuatingrightshoulderweaknesswerealsonoted.He wasalsofoundtohaveelevatedFT3,FT4,andasuppressedTSH.Thyroidultrasoundrevealedthyromegalywithdiffused parenchymal disease. Thyroid scintigraphy showed increased uptake function at 72.4% uptake at 24 h. TRAb was positive at4.1U/L.Patientwasstartedonpyridostigminewhichledtoasignificantreductioninthefrequencyofocularmuscle weakness.Methimazolewasalsoinitiated.Radioactiveiodineat14.9mciwasinstitutedforthedefinitivemanagementof hyperthyroidism. After RAI, there was abatement of the hyperthyroid symptoms, as well as improvement in the status of the myasthenia gravis, with ptosis, diplopia, and right arm weakness hardly occurring thereafter despite the reduction of the pyridostigmine dose based on a symptom diary and medication intake record.
    [Show full text]
  • Myasthenia Gravis
    A Guide for Patients and Families What is... Myasthenia Gravis Myasthenia gravis (MG) is a chronic autoimmune MG is not inherited, and it is not contagious. Although disease — a disease that occurs when the immune MG is not hereditary, genetic susceptibility appears to system mistakenly attacks the body’s own tissues. play a role in it. Occasionally, the disease may occur in more than one member of the same family. In MG, the immune system attacks and interrupts the connection between nerve and muscle, called the MG causes weakness in muscles that control the neuromuscular junction (NMJ). This causes weakness eyes, face, neck, and limbs. Symptoms include partial in the skeletal muscles, which are responsible for paralysis of eye movements, double vision, and droopy breathing and moving parts of the body. eyelids, as well as weakness and fatigue in neck and jaws with problems in chewing, swallowing, and holding In most cases of MG, the immune system targets the up the head. acetylcholine receptor — a protein on muscle cells that is required for muscle contraction. Muscle weakness in MG gets worse with exertion and improves with rest. About 85 percent of people with MG have antibodies against the acetylcholine receptor in their blood. The Approximately 10-20 percent of people with antibodies target and destroy many of the acetylcholine MG experience at least one myasthenic crisis, an receptors on muscle. Consequently, the muscle’s emergency in which the muscles that control breathing response to repeated nerve signals declines with time, weaken to the point where the individual requires a and the muscles become weak and tired.
    [Show full text]
  • Autoimmune Diseases, Treatment, and Contact Lens Wear
    Autoimmune Diseases, Treatment, and Contact Lens Wear Content written by: June Smith-Jeffries – FCLSA, NCLE, COT Content originally published in the Summer 2015 edition of The Eighth Line Table of Contents • Introduction • Autoimmune Diabetes o Type 1 Diabetes Mellitus o Latent Autoimmune Diabetes of Adulthood (LADA) • Sjögren’s Syndrome • Fibromyalgia • Rheumatoid Arthritis (RA) • Systemic Lupus Erythematosus (SLE) • Ankylosing Spondylitis (AS) • Systemic Sclerosis (Scleroderma) • Raynaud’s Phenomenon • Sarcoidosis • Multiple Sclerosis (MS) • Myasthenia Gravis • Ulcerative Colitis • Corticosteroids and Dilated Eye Exams • Post Test Introduction Autoimmune diseases occur when a person’s immune system does not distinguish between healthy tissue and antigens. An antigen is any substance foreign to the body that evokes an immune response. As a result, the body sets off a reaction that destroys normal tissues. Normally the white blood cells in the body’s immune system help to protect against harmful substances such as bacteria, viruses, toxins, cancer cells and blood and tissue from outside the body. These substances contain antigens. The immune system produces antibodies against these antigens that enable it to destroy these damaging substances. 1 | Page An autoimmune disease may affect one or more organ and various types of tissue. Areas often affected by autoimmune diseases include: connective tissues, joints, muscles, blood vessels, the skin and endocrine glands. There is significant overlap in endocrine and autoimmune diseases because many autoimmune diseases originate in an endocrine gland, for instance, type 2 diabetes, thyroid diseases and Addison’s disease. Autoimmune diseases have been found in virtually every organ system in the body. Most autoimmune diseases continue for the lifetime of the patient because there are no cures.
    [Show full text]
  • Ocular Myasthenia: Evaluationof Tensilon Tonography And
    J Neurol Neurosurg Psychiatry: first published as 10.1136/jnnp.33.5.639 on 1 October 1970. Downloaded from J. Neurol. Neurosurg. Psychiat., 33, 1970, 639-646 Ocular myasthenia: evaluation of Tensilon tonography and electronystagmography as diagnostic tests M. J. CAMPBELL, E. SIMPSON, A. L. CROMBIE, AND J. N. WALTON From the Department of Neurology, Regional Neurological Centre, The General Hospital, and the Department of Ophthalmology, Royal Victoria Infirmary, Newcastle upon Tyne SUMMARY The value of electronystagmography (ENG) and of tonography in monitoring the beneficial effect of edrophonium chloride (Tensilon) on the extraocular muscles in myasthenia gravis has been assessed. Studies were performed on 17 patients with myasthenia gravis and on 18 control subjects, of whom nine had extraocular muscle weakness due to myopathic or neurogenic lesions. Electronystagmography recorded the repetitive following movements of the eyes elicited during guest. Protected by copyright. optokinetic nystagmus. Neuromuscular fatigue with the subsequent beneficial response to Tensilon was clearly seen in 50 % of patients with myasthenia. False positive responses were not seen in control subjects but in many of these, as in the remaining myasthenic patients, the amplitude and rate of nystagmus seen in the ENG was very variable. These difficulties suggest that the ENG is of limited value as a diagnostic test in myasthenia gravis. Tonography, recording the intraocular pressure of the eye continuously over four minutes, was found to be of considerable value. We found that the intraocular pressure fell on average by 1-6 to 1-8 mm Hg over a one minute period in the control recordings but increased by a mean of 1 6 mm Hg in patients with myasthenia, with a peak effect 35 seconds after Tensilon.
    [Show full text]
  • Ocular Myasthenia Gravis Associated with Autoimmune Thyroid Disease
    Case Report OCULAR MYASTHENIA GRAVIS ASSOCIATED WITH AUTOIMMUNE THYROID DISEASE Aylin Yaman, M.D.* / Hakan Yaman, M.D., M.S.** * Departm ent o f neurology, İsparta State Hospital, İsparta, Turkey. ** Fam ily Physician, School o f Medicine, Suleyman Dem irel University, İsparta, Turkey. ABSTRACT pathologies is a rare condition but should be taken into consideration. The coincidence of thyroid ophthalmopathy and ocular myasthenia gravis is a defined but rather rare condition. Key Words: Myasthenia gravis, Graves’ disease, Ophthalmopathy, Ocular involvement, A 30-year-old female patient was admitted with Thyrotoxicosis, Thymectomy complaints of weight loss, sweating, palpitation and tremor of both hands for about 4 months. She was diagnosed as having Graves' disease INTRODUCTION with elevated thyroid hormone levels, diffuse hyperplastic thyroid gland with increased iodine, Graves’ disease and myasthenia gravis are both 131 uptake and positive antithyroid antibodies. autoimmune diseases and the coexistence of Two months after the diagnosis of thyroid these two diseases is well recognised. disease, she developed diplopia and in the Myasthenia Gravis is more frequent in patients following days, bilateral ptosis. Orbital magnetic with thyroid disease. It is seen in less than one resonance imaging showed that the lateral and percent of patients with Graves’ disease, and inferior rectus muscles were thickened indicating approximately five percent of myasthenic the infiltration of those muscles. She had positive patients are thyrotoxic at some time (1). response to the prostigmine test and elevated Moreover thyroid diseases occur more frequently acetylcholine receptor antibody levels supporting in close relatives of patients with myasthenia the diagnosis of myasthenia gravis. She had gravis than in the general population (2).
    [Show full text]
  • Myasthenia Gravis Diagnosis and Management
    MyastheniaMyasthenia GravisGravis DiagnosisDiagnosis andand managementmanagement Dr.Dr. ThaninThanin AsawavichienjindaAsawavichienjinda,, M.D.M.D. MyastheniaMyasthenia GravisGravis • A neuromuscular disorder characterized by weakness and fatigability of skeletal muscles • The underlying defect: A decrease in the number of available acetylcholine receptors (AChRs) at neuromuscular junctions due to an antibody-mediated autoimmune attack. •• PreferablePreferable name:name: AutoimmuneAutoimmune myastheniamyasthenia • Treatment now available for MG is highly effective, although a specific cure has remained elusive Harrison 2001 MyastheniaMyasthenia Gravis:Gravis: EpidemiologyEpidemiology •• InIn thethe USA,USA, thethe prevalenceprevalence isis 14.214.2 cases/1cases/1 millionmillion peoplepeople •• AppearAppear atat anyany ageage •• InIn women,women, thethe onsetonset betweenbetween 2020 andand 4040 yearsyears ofof ageage •• AmongAmong men,men, atat 4040--6060 • Overall, women are affected more frequently than men, in a ratio of approximately 3:2. •• FamilialFamilial occurrenceoccurrence isis rarerare JOAO 2004 MyastheniaMyasthenia Gravis:Gravis: EpidemiologyEpidemiology •• AnnualAnnual incidence:incidence: 0.250.25--2/100,0002/100,000 •• SpontaneousSpontaneous remission:remission: 20%20% •• WithoutWithout treatment,treatment, 2020--30%30% diedie inin 1010 yearsyears •• MGMG isis aa heterogeneousheterogeneous disorderdisorder –– 90%90% nono specificspecific causecause •• Genetic predisposing factor: HLA association; HLA-BW46 in chinese ocular
    [Show full text]
  • Thymectomy in Myasthenia Gravis
    Review Rückert JensC et al. Thymectomy in Myasthenia Gravis. Neu- rology International Open 2018; 00: 00–00 Thymectomy in Myasthenia Gravis Authors Jens C. Rückert1, Marc Swierzy1, Siegfried Kohler2, Andreas Meisel2, Mahmoud Ismail1 Affiliation ABSTracT 1 Kompetenzzentrum für Thoraxchirurgie (CCM,CVK,CBF), In recent years much progress has been made in the investiga- Chirurgische Klinik Campus Charité Mitte / Campus tion of the pathophysiology, characterizing subgroups, and Virchow-Klinikum; Charité – Universitätsmedizin Berlin extension of multimodal treatment of myasthenia gravis (MG). 2 Integriertes Myasthenie Zentrum, Klinik für Neurologie, This applies especially to the role of thymectomy (Thx). NeuroCure Clinical Research Center, Charité – Thymectomy is always indicated for thymoma-associated my- Universitätsmedizin Berlin asthenia gravis. Furthermore, based on large cohort studies, during recent decades thymectomy has also become a central Key words part of immune-modulating MG therapy in patients without Thymectomy, robotic, thoracoscopic, sternotomy, thymoma. The lack of randomized studies, however, caused a Myasthenia gravis, thymoma certain persistent reluctance as to the significance of thymec- tomy. The current MGTX trial has shown the effectiveness of Bibliography thymectomy. A significant improvement of myasthenic com- DOI https://doi.org/10.1055/a-0559-2746 plaints and the reduction of immunosuppressive medication Neurology International Open 2018; 2: E124–E130 was primarily shown for acquired early-onset MG (EOMG) with © Georg Thieme Verlag KG Stuttgart · New York complete resection of all thymic tissue. Because the MGTX ISSN 2511-1795 study only included patients younger than 65 years with gen- eralized MG and positive for acetylcholine-receptor antibodies, Correspondence at present the significance of Thx for other relevant subgroups Prof.
    [Show full text]
  • Prevalence and Impact of Autoimmune Thyroid Disease on Myasthenia Gravis Course
    Received: 26 February 2016 | Revised: 12 June 2016 | Accepted: 21 June 2016 DOI: 10.1002/brb3.537 ORIGINAL RESEARCH Prevalence and impact of autoimmune thyroid disease on myasthenia gravis course Justyna Kubiszewska1 | Beata Szyluk1 | Piotr Szczudlik1 | Zbigniew Bartoszewicz2 | Małgorzata Dutkiewicz3 | Maksymilian Bielecki4 | Tomasz Bednarczuk2 | Anna Kostera-Pruszczyk1 1Department of Neurology, Medical University of Warsaw, Warsaw, Poland Abstract 2Department of Internal Medicine and Objectives: Autoimmune thyroid diseases (ATDs) frequently accompany myasthenia Endocrinology, Medical University of gravis (MG) and may influence its course. We aimed to determine the association and Warsaw, Warsaw, Poland impact of ATD with early- (<50 years), late- onset MG, or thymoma- MG. 3Department of Immunology, Biochemistry and Nutrition, Medical University of Materials and Methods: Prevalence of ATD was measured in a cross- sectional study Warsaw, Warsaw, Poland of 343 consecutive patients with MG (236 F, 107 M) aged 4–89 years; 83.8% were 4Department of Psychology, SWPS University of Social Sciences and seropositive, in 2.9%, anti- MuSK antibodies were detected. Concentrations of antithy- Humanities, Warsaw, Poland roid peroxidase antibodies, antithyroglobulin antibodies, antithyrotropin receptor antibodies, and TSH level were measured in all patients. MG clinical course, treatment Correspondence Anna Kostera-Pruszczyk, Department of received, and treatment results were evaluated. Neurology, Medical University of Warsaw, Results: Autoimmune thyroid diseases were diagnosed in 92 (26.8%) of MG patients Warsaw, Poland. Email: [email protected] including 4.4% with Graves (GD), 9% with Hashimoto thyroiditis (HT), and 13.4% with antithyroid antibodies only. GD patients had ocular symptoms more often than patients with antithyroid antibodies or HT (p = .008).
    [Show full text]
  • Neurological Manifestations of Graves' Disease: a Case Report and Review of the Literature
    Published online: 2019-09-25 Case Report Neurological manifestations of Graves’ disease: A case report and review of the literature Swayamsidha Mangaraj, Arun Kumar Choudhury, Binoy Kumar Mohanty, Anoj Kumar Baliarsinha Department of Endocrinology, S. C. B Medical College, Cuttack, Odisha, India ABSTRACT Graves’ disease (GD) is characterized by a hyperfunctioning thyroid gland due to stimulation of the thyroid‑stimulating hormone receptor by autoantibodies directed against it. Apart from thyrotoxicosis, other clinical manifestations include ophthalmopathy, dermopathy, and rarely acropachy. GD is an organ‑specific autoimmune disorder, and hence is associated with various other autoimmune disorders. Myasthenia gravis (MG) is one such disease, which is seen with patients of GD and vice versa. Though the association of GD and myasthenia is known, subtle manifestations of latter can be frequently missed in routine clinical practice. The coexistence of GD and ocular MG poses a significant diagnostic dilemma to treating physicians. The ocular manifestations of myasthenia can be easily missed in case of GD and falsely attributed to thyroid associated ophthalmopathy due to closely mimicking presentations of both. Hence, a high degree of the clinical vigil is necessary in such cases to appreciate their presence. We present a similar case which exemplifies the above said that the clinical challenge in diagnosing coexistent GD and ocular myasthenia. Key words: Graves’ disease, ocular myasthenia, ophthalmopathy, ptosis Introduction Case Report Graves’ disease (GD) is a common endocrine disorder A 38‑year‑old female presented with drooping of both and is the most common cause of spontaneous eyelids and double vision for 20 days. There was some hyperthyroidism.
    [Show full text]
  • Simultaneous Diagnosis of Ocular Myasthenia Gravis and Graves
    Sinapse® | Volume 19 | N.º 3-4 | July-September · October-December 2019 CASO CLÍNICO/CASE REPORT Simultaneous Diagnosis of Ocular Myasthenia Gravis and Graves’ Disease in an Adolescent Female: The Need for Thyroid Evaluation in Myasthenia Gravis Diagnóstico Simultâneo de Miastenia Gravis Ocular e Doença de Graves numa Adolescente: A Necessidade de Avaliação da Função Tiroideia na Miastenia Gravis Daniela Dias1*, Ana Rita Carvalho2, Joana Lima Ferreira3, Inês Melo2, Filipe Palavra4, Alice Mirante2 1-Serviço de Endocrinologia, Instituto Português de Oncologia de Lisboa Francisco Gentil; Lisboa, Portugal 2-Unidade de Endocrinologia Pediátrica, Hospital Pediátrico, Centro Hospitalar e Universitário de Coimbra; Coimbra, Portugal 3-Serviço de Endocrinologia, Hospital Pedro Hispano, ULS Matosinhos; Matosinhos, Portugal 4- Centro de Desenvolvimento da Criança – Neuropediatria, Hospital Pediátrico, Centro Hospitalar e Universitário de Coimbra; Instituto de Investigação Clínica e Biomédica de Coimbra (iCBR), Faculdade de Medicina, Universidade de Coimbra; Coimbra, Portugal Abstract Informações/Informations: Caso Clínico, publicado em The association of ocular myasthenia gravis and Graves’ disease is an uncommon Sinapse, Volume 19, Número 3-4, julho-setembro · outubro- occurrence, but well recognized. It is best described in adults, with only a few reports dezembro 2019. Versão being described in children. We report the case of a 13-year-old girl who presented a eletrónica em www.sinapse.pt Case Report, published in history of general fatigue, binocular diplopia, and bilateral ptosis accentuated on the Sinapse, Volume 19, Number 3-4, july-september · october- right side that affected her predominantly in the evening, with about a month and a december 2019. Electronic version in www.sinapse.pt half of evolution.
    [Show full text]
  • Myasthenia Gravis and Lambert-Eaton Myasthenic Syndrome Review Article Copyright © American Academy of Neurology
    Review Article 04/25/2018 on mAXWo3ZnzwrcFjDdvMDuzVysskaX4mZb8eYMgWVSPGPJOZ9l+mqFwgfuplwVY+jMyQlPQmIFeWtrhxj7jpeO+505hdQh14PDzV4LwkY42MCrzQCKIlw0d1O4YvrWMUvvHuYO4RRbviuuWR5DqyTbTk/icsrdbT0HfRYk7+ZAGvALtKGnuDXDohHaxFFu/7KNo26hIfzU/+BCy16w7w1bDw== by https://journals.lww.com/continuum from Downloaded Downloaded from Address correspondence to https://journals.lww.com/continuum Dr Michael W. Nicolle, London Health Sciences Centre, Myasthenia Gravis University Hospital, 339 Windermere Rd, London, ON N6A 5A5, Canada, and Lambert-Eaton [email protected]. Relationship Disclosure: by mAXWo3ZnzwrcFjDdvMDuzVysskaX4mZb8eYMgWVSPGPJOZ9l+mqFwgfuplwVY+jMyQlPQmIFeWtrhxj7jpeO+505hdQh14PDzV4LwkY42MCrzQCKIlw0d1O4YvrWMUvvHuYO4RRbviuuWR5DqyTbTk/icsrdbT0HfRYk7+ZAGvALtKGnuDXDohHaxFFu/7KNo26hIfzU/+BCy16w7w1bDw== Dr Nicolle has given Myasthenic Syndrome expert medical testimony in court cases for the Canadian Medical Michael W. Nicolle, MD Protective Association. Unlabeled Use of Products/Investigational ABSTRACT Use Disclosure: Dr Nicolle discusses the Purpose of Review: This article discusses the pathogenesis, diagnosis, and management of unlabeled/investigational autoimmune myasthenia gravis (MG) and Lambert-Eaton myasthenic syndrome (LEMS). use of azathioprine, Recent Findings: Recognition of new antigenic targets and improved diagnostic methods mycophenolate, and rituximab for the treatment promise to improve the diagnosis of MG, although the clinical phenotypes associated with of myasthenia gravis and newer antibodies have not yet been defined. Future therapies
    [Show full text]