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  Vol. 128 No. 8, August 1993 TABLE OF CONTENTS
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  Papers Presented at the 100th Scientific Session of the Western Surgical Association, San Antonio, Tex, November 15-18, 1992, Part II
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Thymectomy for Myasthenia Gravis

Geoffrey B. Blossom, MD; Raina M. Ernstoff, MD; Gregory A. Howells, MD; Phillip J. Bendick, PhD; John L. Glover

Arch Surg. 1993;128(8):855-862.


Abstract

Objectives
To assess the change in clinical status of patients with generalized myasthenia gravis treated with thymectomy and to identify prognostic variables that may be of significance in optimizing patient selection.

Design
Retrospective review. Mean follow-up period was 41 months.

Setting
Large community hospital.

Patients
Thirty-seven patients (11 male and 26 female) with generalized myasthenia gravis who were referred for thymectomy if they were refractory to medical treatment or had a thymoma. This represents all patients undergoing thymectomy for myasthenia gravis between January 1982 and December 1991.

Interventions
Each patient underwent staging before and after thymectomy using a modified Osserman classification. Medication requirements were also recorded. All patients underwent transsternal thymectomy and complete mediastinal dissection.

Main Outcome Measures
Changes in clinical stage and medication requirement before and after thymectomy; effect of patient age, sex, duration of disease, stage of disease, antibody status, histologic characteristics of the thymus, and duration of follow-up on outcome.

Results
Improvement after thymectomy was noted in all 37 patients. Complete remission was achieved in three patients (8%) and pharmacologic remission in 23 (62%). The remainder improved in stage, medication requirement, or both. Patients in preoperative stages lib and IIc showed the greatest improvement. Age, sex, duration of disease, antibody status, histologic characteristics of the thymus, and duration of follow-up were not significant factors in assessing improvement.

Conclusions
Transsternal thymectomy was found to be beneficial to all patients with generalized myasthenia gravis. Complete or pharmacologic remission was achieved in most patients (70%) following the procedure. Patients in preoperative stages lib and IIc showed the greatest degree of postoperative improvement.

(Arch Surg. 1993;128:855-862)



Author Affiliations

From the Departments of Surgery (Drs Blossom, Howells, Bendick, and Glover) and Neurology (Dr Ernstoff), William Beaumont Hospital, Royal Oak, Mich.



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