Inferior oblique muscle paresis as a sign of myasthenia gravis

Yehoshua Almog, Merav Ben-David, Arie Y. Nemet

Research output: Contribution to journalArticlepeer-review

12 Scopus citations

Abstract

Myasthenia gravis may affect any of the six extra-ocular muscles, masquerading as any type of ocular motor pathology. The frequency of involvement of each muscle is not well established in the medical literature. This study was designed to determine whether a specific muscle or combination of muscles tends to be predominantly affected. This retrospective review included 30 patients with a clinical diagnosis of myasthenia gravis who had extra-ocular muscle involvement with diplopia at presentation. The diagnosis was confirmed by at least one of the following tests: Tensilon test, acetylcholine receptor antibodies, thymoma on chest CT scan, or suggestive electromyography. Frequency of involvement of each muscle in this cohort was inferior oblique 19 (63.3%), lateral rectus nine (30%), superior rectus four (13.3%), inferior rectus six (20%), medial rectus four (13.3%), and superior oblique three (10%). The inferior oblique was involved more often than any other muscle (p < 0.01). Eighteen (60%) patients had ptosis, six (20%) of whom had bilateral ptosis. Diagnosing myasthenia gravis can be difficult, because the disease may mimic every pupil-sparing pattern of ocular misalignment. In addition diplopia caused by paresis of the inferior oblique muscle is rarely encountered (other than as a part of oculomotor nerve palsy). Hence, when a patient presents with vertical diplopia resulting from an isolated inferior oblique palsy, myasthenic etiology should be highly suspected.

Original languageEnglish
Pages (from-to)50-53
Number of pages4
JournalJournal of Clinical Neuroscience
Volume25
DOIs
StatePublished - 1 Mar 2016
Externally publishedYes

Keywords

  • Diplopia
  • Extra-ocular muscles
  • Inferior oblique palsy
  • Myasthenia gravis
  • Ptosis

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