A case of diplopia and arm weakness

A brainstem lesion, such as a tumour or stroke, could cause similar cranial symptoms but would typically also result in long tract signs and possibly additional features such as sensory impairment and ataxia. 3 Investigations and management Investigation to confirm the diagnosis in cases of suspecte...

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Bibliographic Details
Published inBMJ Vol. 339; no. nov25 2; p. b4555
Main Authors Sennik, D K, Suresh, D, Goodall, E, Lane, R J M
Format Journal Article
LanguageEnglish
Published England British Medical Journal Publishing Group 25.11.2009
BMJ Publishing Group LTD
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Summary:A brainstem lesion, such as a tumour or stroke, could cause similar cranial symptoms but would typically also result in long tract signs and possibly additional features such as sensory impairment and ataxia. 3 Investigations and management Investigation to confirm the diagnosis in cases of suspected myasthenia gravis should include the edrophonium (Tensilon) test, electromyography, and measurement of serum acetylcholine receptor antibodies. 1 2 Our patient had an edrophonium (Tensilon) test (figs 3-6 ), and ptosis improved greatly one minute after administration of the drug (fig 4). 10 Alternative immunosuppressants include methotrexate, cyclophosphamide, mycophenolate mofetil, or tacrolimus, but the evidence base for these is lacking. 10 There are case reports that rituximab, a monoclonal antibody that suppresses B cells, is beneficial in refractory cases. 11 Patients on long term steroids should be considered for bone protection treatment. 12 Acute myasthenic crisis-characterised by rapid exacerbation of symptoms of weakness, with or without respiratory muscle involvement-can be treated with plasma exchange or intravenous immunoglobulins. 1 The thymus regulates immune tolerance and the removal of T cells that respond to self antigens.
Bibliography:href:bmj-339-bmj-b4555.pdf
ArticleID:send713669
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PMID:19939896
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ObjectType-Case Study-2
SourceType-Scholarly Journals-1
ObjectType-Feature-4
content type line 23
ObjectType-Report-1
ObjectType-Article-3
ISSN:0959-8138
1468-5833
1756-1833
DOI:10.1136/bmj.b4555