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The Journal of Thoracic and Cardiovascular Surgery, Vol 80, 696-701, Copyright © 1980 by The American Association for Thoracic Surgery and The Western Thoracic Surgical Association
RE Clark, JP Marbarger, PN West, JA Spratt, JM Florence, CL Roper, TB Ferguson and CS Weldon
An 8 year experience with a prospective treatment program for patients with
myasthenia gravis is reviewed with particular focus on the results in
patients less than 35 years of age. Twenty myasthenic young adults with an
average age of 24 years and a duration of symptoms of 22 months, excluding
two with the juvenile form, had thymectomy followed by short-term
anticholinesterase and long-term prednisone therapy. All of the 18 patients
with a short duration of symptoms are in markedly improved condition and
61% of them are in remission after a mean postoperative period of 32
months. The longest follow-up period is 7.3 years. Two patients have mild
improvement. There was no correlation between thymic disease and clinical
result. Complete en bloc extirpation of all thymic and adjacent tissue
through a median sternotomy is advocated. The patients were treated
postoperatively with prednisone, 100 mg/day, a regimen which gradually is
changed to every other day medication and finally a gradual reduction of
dosage. There have been no operative or late deaths and no serious
complications of therapy. The effects have been long lasting, with not a
single instance of significant recurrence of symptoms of myasthenia gravis
6 months after thymectomy.
ARTICLES
Thymectomy for myasthenia gravis in the young adult. Long-term results
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A. K. Afifi and W. E. Bell Tests for Juvenile Myasthenia Gravis: Comparative Diagnostic Yield and Prediction of Outcome J Child Neurol, October 1, 1993; 8(4): 403 - 411. [Abstract] [PDF] |
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