Skip to main content
Top
Published in: Journal of Medical Case Reports 1/2014

Open Access 01-12-2014 | Case report

Double seronegative myasthenia gravis with antiphospholipid syndrome: a case report

Authors: Diana Dan, Pierre-Alexandre Bart, Jan Novy, Thierry Kuntzer, Carole Clair

Published in: Journal of Medical Case Reports | Issue 1/2014

Login to get access

Abstract

Introduction

Myasthenia gravis is an autoimmune disease characterized by fluctuating muscle weakness. It is often associated with other autoimmune disorders, such as thyroid disease, rheumatoid arthritis, systemic lupus erythematosus, and antiphospholipid syndrome. Many aspects of autoimmune diseases are not completely understood, particularly when they occur in association, which suggests a common pathogenetic mechanism.

Case presentation

We report a case of a 42-year-old Caucasian woman with antiphospholipid syndrome, in whom myasthenia gravis developed years later. She tested negative for both antibodies against the acetylcholine receptor and against muscle-specific receptor tyrosine-kinase, but had typical decremental responses at the repetitive nerve stimulation testing, so that a generalized myasthenia gravis was diagnosed. Her thromboplastin time and activated partial thromboplastin time were high, anticardiolipin and anti-β2 glycoprotein-I antibodies were slightly elevated, as a manifestation of the antiphospholipid syndrome. She had a good clinical response when treated with a combination of pyridostigmine, prednisone and azathioprine.

Conclusions

Many patients with myasthenia gravis test positive for a large variety of auto-antibodies, testifying of an immune dysregulation, and some display mild T-cell lymphopenia associated with hypergammaglobulinemia and B-cell hyper-reactivity. Both of these mechanisms could explain the occurrence of another autoimmune condition, such as antiphospholipid syndrome, but further studies are necessary to shed light on this matter.
Clinicians should be aware that patients with an autoimmune diagnosis such as antiphospholipid syndrome who develop signs and neurological symptoms suggestive of myasthenia gravis are at risk and should prompt an emergent evaluation by a specialist.
Literature
1.
2.
go back to reference Vincent A, Palace J, Hilton-Jones D: Myasthenia gravis. Lancet. 2001, 357: 2122-2128. 10.1016/S0140-6736(00)05186-2.CrossRefPubMed Vincent A, Palace J, Hilton-Jones D: Myasthenia gravis. Lancet. 2001, 357: 2122-2128. 10.1016/S0140-6736(00)05186-2.CrossRefPubMed
3.
go back to reference Vincent A: Unravelling the pathogenesis of myasthenia gravis. Nat Rev Immunol. 2002, 2: 797-804. 10.1038/nri916.CrossRefPubMed Vincent A: Unravelling the pathogenesis of myasthenia gravis. Nat Rev Immunol. 2002, 2: 797-804. 10.1038/nri916.CrossRefPubMed
4.
go back to reference Evoli A, Padua L: Diagnosis and therapy of myasthenia gravis with antibodies to muscle-specific kinase. Autoimmun Rev. 2013, 12: 931-935. 10.1016/j.autrev.2013.03.004.CrossRefPubMed Evoli A, Padua L: Diagnosis and therapy of myasthenia gravis with antibodies to muscle-specific kinase. Autoimmun Rev. 2013, 12: 931-935. 10.1016/j.autrev.2013.03.004.CrossRefPubMed
5.
go back to reference Mori S, Shigemoto K: Mechanisms associated with the pathogenicity of antibodies against muscle-specific kinase in myasthenia gravis. Autoimmun Rev. 2013, 12: 912-917. 10.1016/j.autrev.2013.03.005.CrossRefPubMed Mori S, Shigemoto K: Mechanisms associated with the pathogenicity of antibodies against muscle-specific kinase in myasthenia gravis. Autoimmun Rev. 2013, 12: 912-917. 10.1016/j.autrev.2013.03.005.CrossRefPubMed
6.
go back to reference Zisimopoulou B, Brenner T, Trakas N, Tzartos SJ: Serological diagnostics in myasthenia gravis based on novel assays and recently identified antigens. Autoimmun Rev. 2013, 12: 924-930. 10.1016/j.autrev.2013.03.002.CrossRefPubMed Zisimopoulou B, Brenner T, Trakas N, Tzartos SJ: Serological diagnostics in myasthenia gravis based on novel assays and recently identified antigens. Autoimmun Rev. 2013, 12: 924-930. 10.1016/j.autrev.2013.03.002.CrossRefPubMed
7.
go back to reference Muppidi S, Wolfe GI: Muscle-specific receptor tyrosine kinase antibody-positive and seronegative myasthenia gravis. Front Neurol Neurosci. 2009, 26: 109-119.CrossRefPubMed Muppidi S, Wolfe GI: Muscle-specific receptor tyrosine kinase antibody-positive and seronegative myasthenia gravis. Front Neurol Neurosci. 2009, 26: 109-119.CrossRefPubMed
8.
go back to reference Chan KH, Lachance DH, Harper CM, Lennon VA: Frequency of seronegativity in adult-acquired generalized myasthenia gravis. Muscle Nerve. 2007, 36: 651-658. 10.1002/mus.20854.CrossRefPubMed Chan KH, Lachance DH, Harper CM, Lennon VA: Frequency of seronegativity in adult-acquired generalized myasthenia gravis. Muscle Nerve. 2007, 36: 651-658. 10.1002/mus.20854.CrossRefPubMed
10.
go back to reference Evoli A, Batocchi AP, Lo Monaco M, Servidei S, Padua L, Majolini L, Tonali P: Clinical heterogeneity of seronegative myasthenia gravis. Neuromuscul Disord. 1996, 6: 155-161. 10.1016/0960-8966(96)00009-0.CrossRefPubMed Evoli A, Batocchi AP, Lo Monaco M, Servidei S, Padua L, Majolini L, Tonali P: Clinical heterogeneity of seronegative myasthenia gravis. Neuromuscul Disord. 1996, 6: 155-161. 10.1016/0960-8966(96)00009-0.CrossRefPubMed
11.
go back to reference Mossman S, Vincent A, Newsom-Davis J: Myasthenia gravis without acetylcholine-receptor antibody: a distinct disease entity. Lancet. 1986, 1: 116-119.CrossRefPubMed Mossman S, Vincent A, Newsom-Davis J: Myasthenia gravis without acetylcholine-receptor antibody: a distinct disease entity. Lancet. 1986, 1: 116-119.CrossRefPubMed
13.
go back to reference Kaji M, Sato Y, Kunoh H, Watanabe A, Aizawa H, Oizumi K, Abe T: Antiphospholipid syndrome and multiple ischemic strokes in a patient with myasthenia gravis. Kurume Med J. 2002, 49: 211-216. 10.2739/kurumemedj.49.211.CrossRefPubMed Kaji M, Sato Y, Kunoh H, Watanabe A, Aizawa H, Oizumi K, Abe T: Antiphospholipid syndrome and multiple ischemic strokes in a patient with myasthenia gravis. Kurume Med J. 2002, 49: 211-216. 10.2739/kurumemedj.49.211.CrossRefPubMed
14.
go back to reference Shoenfeld Y, Lorber M, Yucel T, Yazici H: Primary antiphospholipid syndrome emerging following thymectomy for myasthenia gravis: additional evidence for the kaleidoscope of autoimmunity. Lupus. 1997, 6: 474-476. 10.1177/096120339700600511.CrossRefPubMed Shoenfeld Y, Lorber M, Yucel T, Yazici H: Primary antiphospholipid syndrome emerging following thymectomy for myasthenia gravis: additional evidence for the kaleidoscope of autoimmunity. Lupus. 1997, 6: 474-476. 10.1177/096120339700600511.CrossRefPubMed
15.
go back to reference Watanabe H, Hakusui S, Yanagi T, Yoshida A, Yasuda T: A case of antiphospholipid syndrome associated with myasthenia gravis. Rinsho Shinkeigaku. 1997, 37: 641-644. JapanesePubMed Watanabe H, Hakusui S, Yanagi T, Yoshida A, Yasuda T: A case of antiphospholipid syndrome associated with myasthenia gravis. Rinsho Shinkeigaku. 1997, 37: 641-644. JapanesePubMed
16.
go back to reference Sanmarco M, Bernard D: Studies of IgG-class anticardiolipin antibodies in myasthenia gravis. Autoimmunity. 1994, 18: 57-63. 10.3109/08916939409014680.CrossRefPubMed Sanmarco M, Bernard D: Studies of IgG-class anticardiolipin antibodies in myasthenia gravis. Autoimmunity. 1994, 18: 57-63. 10.3109/08916939409014680.CrossRefPubMed
Metadata
Title
Double seronegative myasthenia gravis with antiphospholipid syndrome: a case report
Authors
Diana Dan
Pierre-Alexandre Bart
Jan Novy
Thierry Kuntzer
Carole Clair
Publication date
01-12-2014
Publisher
BioMed Central
Published in
Journal of Medical Case Reports / Issue 1/2014
Electronic ISSN: 1752-1947
DOI
https://doi.org/10.1186/1752-1947-8-2

Other articles of this Issue 1/2014

Journal of Medical Case Reports 1/2014 Go to the issue