Treatment of acromegaly, Cushing disease and Nelson syndrome

West J Med. 1980 Sep;133(3):197-202.

Abstract

Since 1957 we have treated more than 429 patients who had pituitary neoplasms, most of which were hormone-secreting tumors. Long-term follow-up in the large group of patients treated for acromegaly shows a median survival of better than 16 years, with improvement over time. The short-term follow-up results in patients with Cushing* disease, Nelson syndrome and chromophobe adenoma are very encouraging. To compare these excellent results with those following surgical procedures, a large study of patients followed for a long period after the operations is needed.

MeSH terms

  • Acromegaly / radiotherapy*
  • Adenoma, Chromophobe / radiotherapy*
  • Adolescent
  • Adult
  • Cushing Syndrome / radiotherapy*
  • Female
  • Humans
  • Male
  • Middle Aged
  • Nelson Syndrome / radiotherapy*
  • Pituitary Neoplasms / radiotherapy*