Literature DB >> 33401082

Subclinical myasthenia gravis in thymomas.

Florit Marcuse1, Monique Hochstenbag2, Janneke G J Hoeijmakers3, Myrurgia Abdul Hamid4, Jan Damoiseaux5, Jos Maessen6, Marc De Baets7.   

Abstract

BACKGROUND: A proportion of thymoma-patients without a history of myasthenia gravis (MG) before thymectomy, appears to have positive anti-AChR-antibodies in the serum. These subclinical MG-patients could be underdiagnosed because analyzation of anti-AChR-antibodies in thymomas is not always performed in patients who did not experience neurological symptoms. The prevalence and long-term outcomes of subclinical MG are never described in literature yet.
METHODS: We retrospectively analyzed 398 consecutive patients who underwent a robotic-assisted thoracoscopic surgery at the Maastricht University Medical Center+ (MUMC+) between April 2004 and December 2018. In the MUMC+, a robotic approach is the standard surgical approach in patients with thymic diseases. Inclusion criteria were thymomas, thymectomy performed in the MUMC + with a follow-up of at least one year and age above 18 years old. Exclusion criteria were patients with thymic carcinomas, refused participation, or those who were lost to follow-up.
RESULTS: Of the 102 included thymoma-patients, 87 patients (85 %) were tested for anti-AChR-antibodies before thymectomy, of which 57 patients were diagnosed with clinical MG and seven subclinical MG-patients were found. Of the 15 patients who were not tested for anti-AChR-antibodies, four more subclinical MG-patients were discovered in the years after thymectomy. The median follow-up time was 62 months. In total, 11 subclinical MG-patients were found, with a mean age of 54 years and predominantly females (64 %). Ten subclinical MG-patients (91 %) developed clinical-MG, within six years after thymectomy. Immunosuppressive drugs were prescribed in five patients. Four patients were diagnosed with a recurrence of the thymoma. No surgical mortality was reported. Two patients died due to a myasthenic crisis.
CONCLUSIONS: The prevalence of subclinical MG in thymomas was found to be 10.8 %. One in four patients who experienced no neurological symptoms before thymectomy, appeared to have anti-AChR-antibodies and 91 % of these patients developed clinical MG within six years after the thymectomy. Analyzing anti-AChR-antibodies in the serum is recommended in all suspected thymomas before a thymectomy is performed.
Copyright © 2020 Elsevier B.V. All rights reserved.

Entities:  

Keywords:  Anti-acetylcholinereceptor-antibodies; Myasthenia gravis; Thymectomy; Thymomas

Mesh:

Year:  2020        PMID: 33401082     DOI: 10.1016/j.lungcan.2020.12.010

Source DB:  PubMed          Journal:  Lung Cancer        ISSN: 0169-5002            Impact factor:   5.705


  2 in total

1.  Relationship between anti-acetylcholine receptor antibodies and the development of post-thymectomy myasthenia gravis in patients with thymoma: a single-center experience.

Authors:  Yusuke Nabe; Teppei Hashimoto; Kanji Tanaka; Yasuhiro Fujita; Katsuma Yoshimatsu; Yukiko Nemoto; Rintaro Oyama; Hiroki Matsumiya; Masataka Mori; Masatoshi Kanayama; Akihiro Taira; Shinji Shinohara; Taiji Kuwata; Masaru Takenaka; Yuko Tashima; Koji Kuroda; Fumihiro Tanaka
Journal:  Gland Surg       Date:  2021-08

2.  The association between anti-acetylcholine receptor antibody level and clinical improvement in myasthenia gravis.

Authors:  Florit Marcuse; Lloyd Brandts; Daan Moens; Jan Damoiseaux; Monique Hochstenbag; Janneke G J Hoeijmakers; Jos G Maessen; Marc De Baets
Journal:  Eur J Neurol       Date:  2022-01-09       Impact factor: 6.288

  2 in total

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