Pituitary & hypothalamus

Clinical and Pathological Spectrum of Acromegaly: Distinguishing GH Pituitary Neuroendocrine Tumor (PitNETs), Mammosomatotrophs, and Mixed Tumors

J Clin Endocrinol MetabPublished Cross-sectional study

Authors' conclusion

These findings highlight the heterogeneity within GH&PRL PitNETs, including silent PRL-positive GH PitNETs. Our data suggest mixed SL tumors may be less responsive to SSTR ligands, emphasizing the need for tailored strategies based on tumor subtype and receptor profile.

Study context

Population
Patients with acromegaly with PitNETs
Participants
51 PitNETs
Exposure
GH PitNETs vs mammosomatotrophs vs mixed SL PitNETs
  • GH PitNETsn = 23
  • Mammosomatotrophsn = 20
  • Mixed SL PitNETsn = 8
Outcome
Clinical and molecular differences between subtypes
Methodological detailsdouble immunofluorescence, clinicopathological correlation
  • Double immunofluorescence
  • Clinicopathological correlation

Main finding

As reported in the abstract

Prolactin (PRL)-positive tumors without hyperprolactinemia (silent PRL-positive GH PitNETs)

41%

Observational data: associations, not effects.

Original publication

Clinical and Pathological Spectrum of Acromegaly: Distinguishing GH PitNETs, Mammosomatotrophs, and Mixed Tumors. J Clin Endocrinol Metab. Published 26 November 2025. doi:10.1210/clinem/dgaf634

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