Background: There has been little previous study reporting the eye findings
and presentation of elderly patients with myasthenia gravis. The purpose o
f this study was to review the findings and course of myasthenia gravis aft
er the sixth decade of life.
Methods: Retrospective observational case series. The authors reviewed the
clinical records of 27 patients with onset of myasthenia gravis at age 60 y
ears or more who were seen at a tertiary care academic ophthalmology centre
in Houston between January 1992 and March 1999. The diagnosis of myastheni
a gravis was based on conventional clinical and laboratory criteria.
Results: Twenty patients (74%) were men. Of the 16 patients who underwent t
esting for anti-acetylcholine receptor antibodies, 11 (69%) were seropositi
ve. Concurrent thyroid disease was found in seven patients (26%), including
five (71%) of the seven women. No patient had thymoma. Sixteen patients (5
9%) manifested generalized symptoms during follow-up; 12 did so within 1 ye
ar of disease onset. Patients responded well to both anticholinesterase and
corticosteroid therapy. At the most recent follow-up visit 18 patients (67
%) were clinically improved, and no patient was clinically worse.
Interpretation: Myasthenia gravis in this study was characterized by a male
predominance, high rate of concurrent thyroid disease, high rate of progre
ssion to mild generalized symptoms, absence of thymoma, good response to me
dical therapy and minimal life-threatening complications. Clinicians should
consider the diagnosis of myasthenia gravis in an older patient presenting
with diplopia or ptosis.