Skip to main content

Advertisement

Log in

Myasthenia gravis with thymoma and autoimmune haemolytic anaemia. A case report

  • CASE REPORT
  • Published:
Neurological Sciences Aims and scope Submit manuscript

Abstract.

Myasthenia gravis is an autoimmune disorder that affects the neuromuscular junction and leads to weakness of the skeletal muscles. Associated autoimmune diseases such as systemic lupus erythematosus, rheumatoid arthritis and pernicious anaemia are present in approximately 5% of the myasthenic patients. This report presents a 64-year-old man with autoimmune haemolytic anemia associated with myasthenia gravis and thymoma. The patient developed a severe Coomb's positive autoimmune haemolytic anaemia, which was resistant to treatment with large doses of prednisone. Haemolytic anaemia entered remission one month following thymectomy, and the patient has maintained a normal haemoglobin and a negative Coomb's test without the need for steroid or immunosuppressive therapy. In conclusion, thymectomy may induce a striking improvement of therapyresistant autoimmune haemolytic anemia in patients with MG and thymoma, but in terms of remission, a long follow-up is needed as autoimmune diseases can show spontaneous fluctuations.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Similar content being viewed by others

Author information

Authors and Affiliations

Authors

Additional information

Received: 19 December 2001 / Accepted in revised form: 27 December 2002

Correspondence to: N. Tuncer Elmaci

Rights and permissions

Reprints and permissions

About this article

Cite this article

Tuncer Elmaci, N., Ratip, S., İnce-Günal, D. et al. Myasthenia gravis with thymoma and autoimmune haemolytic anaemia. A case report. Neurol Sci 24, 34–36 (2003). https://doi.org/10.1007/s100720300019

Download citation

  • Issue Date:

  • DOI: https://doi.org/10.1007/s100720300019

Navigation