Myasthenia gravis associated with thymoma: clinical characteristics and long-term outcome

Mt Palmisani, Amelia Evoli Stampanoni-B, Anna Paola Batocchi, Carlo Provenzano, Pietro Attilio Tonali

Research output: Contribution to journalArticle

17 Citations (Scopus)


We studied 111 myasthenic patients with thymoma followed over the last 20 years. Most patients were affected with severe myasthenia gravis (MG) and had been treated with immunosuppressive drugs. At the end of the follow-up, we observed good therapeutic results in 74% of patients, but a complete remission in only 10% of cases. The survival rate in thymoma patients was significantly lower than in nonthymoma cases. Clinical parameters, MG response to treatment and survival rate did not differ in patients with invasive and noninvasive thymic neoplasms. Patients with invasive thymoma showed slightly higher surgical mortality and a 10% incidence of tumor relapse.
Original languageEnglish
Pages (from-to)78-82
Number of pages5
JournalEuropean Neurology
Publication statusPublished - 1994


  • Follow-Up Studies
  • Myasthenia Gravis
  • Thymectomy
  • Thymoma


Dive into the research topics of 'Myasthenia gravis associated with thymoma: clinical characteristics and long-term outcome'. Together they form a unique fingerprint.

Cite this