Endocrinology, Diabetes & Metabolism Case Reports (Oct 2016)

Late presentation of acromegaly in medically controlled prolactinoma patients

  • Ekaterina Manuylova,
  • Laura M Calvi,
  • Catherine Hastings,
  • G Edward Vates,
  • Mahlon D Johnson,
  • William T Cave Jr,
  • Ismat Shafiq

DOI
https://doi.org/10.1530/edm-16-0069
Journal volume & issue
Vol. 1, no. 1
pp. 1 – 6

Abstract

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Co-secretion of growth hormone (GH) and prolactin (PRL) from a single pituitary adenoma is common. In fact, up to 25% of patients with acromegaly may have PRL co-secretion. The prevalence of acromegaly among patients with a newly diagnosed prolactinoma is unknown. Given the possibility of mixed GH and PRL co-secretion, the current recommendation is to obtain an insulin-like growth factor-1 (IGF-1) in patients with prolactinoma at the initial diagnosis. Long-term follow-up of IGF-1 is not routinely done. Here, we report two cases of well-controlled prolactinoma on dopamine agonists with the development of acromegaly 10–20 years after the initial diagnoses. In both patients, a mixed PRL/GH-cosecreting adenoma was confirmed on the pathology examination after transsphenoidal surgery (TSS). Therefore, periodic routine measurements of IGF-1 should be considered regardless of the duration and biochemical control of prolactinoma.