Thymoma natural history

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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1] Associate Editor(s)-in-Chief: Amr Marawan, M.D. [2] Ahmad Al Maradni, M.D. [3]

Overview

  • If left untreated, thymoma may progress to invade the mediastinum and the surrounding structures.
  • Depending on the stage of the tumor at the time of diagnosis, the prognosis may vary.
  • The prognosis is generally regarded as good.
  • Common complications of thymoma include the pressure effect of the mass itself, autoimmune diseases, and rarely, progression to malignancy.

Natural History, Complications and Prognosis

Natural history

  • One-third of patients have their thymomas discovered because of an associated autoimmune disorder. The most common of those conditions is myasthenia gravis: 10–15% of patients with myasthenia gravis have thymoma. Conversely, 30–45% of patients with thymomas have myasthenia gravis.
  • Patients with thymoma demonstrate a tendency for local mediastinal recurrence and plural ‘‘droplet’’ recurrence presumably caused by mediastinal plural invasion after resection.[1]

Complications

Complications associated with thymoma may include:

Complications of Radiotherapy

The most common complications of radiotherapy are:[1]

Complications of Surgery

The most common complications of thymectomy are:

  • Complications of the procedure such as bleeding, infection, damage to other organs, nerve injuries (bilateral phrenic nerve injury), and respiratory failure.
  • Recurrence has been described 10 to 20 years after removal of the primary lesion, so long-term follow up is very important.
  • Live attenuated vaccines such as yellow fever vaccine may have adverse effects after thymectomy due to an inadequate T-cell response.

Complications of Thymic Biopsy

The complications of thymic biopsy include:

Prognosis

The prognosis of thymoma depends on the following:

  • Location of the tumor
  • Stage of the tumor
  • The prognosis is much worse for stage III or IV thymomas as compared with stage I and II tumors.
  • Patients with stage III and IV tumors may nonetheless survive for several years with appropriate oncological management.
  • Resectability of the tumor
  • Patient's general health
  • Primary diagnosis vs. recurrence
  • Histologic type (mixed histologic type is associated with the worst prognosis)[1]

References

  1. 1.0 1.1 1.2 "Results of surgical treatment for t... [J Thorac Cardiovasc Surg. 1984] - PubMed - NCBI".
  2. Thomas CR, Wright CD, Loehrer PJ (1999). "Thymoma: state of the art". Journal of Clinical Oncology : Official Journal of the American Society of Clinical Oncology. 17 (7): 2280–9. PMID 10561285. Text "accessdate" ignored (help); Unknown parameter |month= ignored (help)

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