Increased incidence of neoplasia in females with acromegaly

Clin Endocrinol (Oxf). 1997 Sep;47(3):323-7. doi: 10.1046/j.1365-2265.1997.2561053.x.


Objective: Some studies have indicated an increased incidence of neoplasia, particularly breast and colon, in acromegaly. We have determined the incidence of benign and malignant neoplasms in an Australian population of patients with acromegaly.

Design: Retrospective review, with comparison against cancer data for the local population obtained from a State Cancer Registry.

Patients: Fifty patients with documented acromegaly.

Results: There were 7 cases of malignancy (2 in men, 5 in women) in the period of follow-up (435 patient years). With logistic regression analysis, there was a relative risk of malignancy, of 1.2 (95% confidence interval 0.31-5.0) for men (P = 0.8) and 4.3 (95% confidence interval 1.7-10.5) for women (P = 0.001), when compared to the local population. There were 2 cases of breast and renal carcinoma, and one each of prostatic, colonic and parotid carcinoma. Of the most common benign tumours 35% of patients had thyroid nodules, 10% had colonic polyps and 6% had nasal polyps.

Conclusion: The incidence of malignancy was found to be increased in female patients with acromegaly in this series. Routine screening procedures for malignancy, particularly in female patients, should therefore be considered.

MeSH terms

  • Acromegaly / complications*
  • Adult
  • Aged
  • Aged, 80 and over
  • Australia / epidemiology
  • Breast Neoplasms / complications
  • Breast Neoplasms / epidemiology
  • Colonic Neoplasms / complications
  • Colonic Neoplasms / epidemiology
  • Female
  • Humans
  • Incidence
  • Kidney Neoplasms / complications
  • Kidney Neoplasms / epidemiology
  • Male
  • Middle Aged
  • Neoplasms / complications*
  • Neoplasms / epidemiology*
  • Parotid Neoplasms / complications
  • Parotid Neoplasms / epidemiology
  • Prostatic Neoplasms / complications
  • Prostatic Neoplasms / epidemiology
  • Regression Analysis
  • Retrospective Studies
  • Risk
  • Sex Factors