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Outcomes after Thymectomy in Patients with Thymomatous Myasthenia Gravis

Objectives  This article describes the clinical outcomes after thymectomy in patients with thymomatous myasthenia gravis (T-MG) managed in the department of thoracic surgery of Hassan II University Hospital of Fez, Fez, Morocco. Materials and Methods  We performed a retrospective analysis of medical...

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Detalles Bibliográficos
Autores principales: Rabiou, Sani, Toudou-Daouda, Moussa, Lakranbi, Marwane, Issoufou, Ibrahim, Ouadnouni, Yassine, Smahi, Mohamed
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Thieme Medical and Scientific Publishers Pvt. Ltd. 2022
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9187376/
https://www.ncbi.nlm.nih.gov/pubmed/35694069
http://dx.doi.org/10.1055/s-0042-1743444
Descripción
Sumario:Objectives  This article describes the clinical outcomes after thymectomy in patients with thymomatous myasthenia gravis (T-MG) managed in the department of thoracic surgery of Hassan II University Hospital of Fez, Fez, Morocco. Materials and Methods  We performed a retrospective analysis of medical records of 16 patients with T-MG between January 2009 and January 2017. Results  There were 11 women and 5 men with a median age of 40 years at the thymectomy time and a median time of onset of symptoms to thymectomy of 12 months. At the preoperative evaluation (Myasthenia Gravis Foundation of America [MGFA] clinical classification), 7 patients were class II, 7 class III, and 2 class IV. Nine patients were in Masaoka stage I, and the remaining 7 patients stage II. We recorded one case of postoperative myasthenic crisis. At 3 years of follow-up after thymectomy, 6 patients had complete stable remission and the other 10 patients improved. Of these patients with clinical improvement, 6 patients were in MGFA class I and the remaining 4 patients class II. Conclusion  The present study shows the beneficial effect of thymectomy in patients with T-MG. Postoperative clinical outcomes seem to be better when the preoperative severity of myasthenic symptoms is mild (MGFA class II).