Skip to main content

Somatotroph Tumor

  • Living reference work entry
  • First Online:
  • 16 Accesses

Part of the book series: Encyclopedia of Pathology ((EP))

Synonyms

GHoma; Growth hormone cell tumor; Somatotroph adenoma

Definition

A neoplasm arising in adenohypophysial tissue that is composed of epithelial neuroendocrine cells of PIT1-lineage that express PIT1 and growth hormone (Asa and Perry 2020).

Clinical Features

  • Incidence

    These tumors represent approximately 12% of surgically resected pituitary neuroendocrine tumors (Mete et al. 2018). They are almost evenly divided between densely granulated and sparsely granulated variants.

  • Age

    Somatotroph tumors can occur at almost any age; the mean age at diagnosis is 50 years for densely granulated tumors and 40 years for sparsely granulated tumors (Mete et al. 2018). However, these ages reflect what is known to be an average of a 10-year delay from onset of signs and symptoms to diagnosis.

  • Sex

    There is no gender predilection for these tumors.

  • Site

    Somatotroph tumors usually arise in the sella turcica. They are usually macrotumors (>1 cm) at the time of diagnosis. They may arise in the sphenoid...

This is a preview of subscription content, log in via an institution.

References and Further Reading

  • Asa, S. L., & Perry, A. (2020). Tumors of the pituitary gland (AFIP atlas of tumor pathology, series 5). Silver Spring: ARP Press.

    Google Scholar 

  • Asa, S. L., Kucharczyk, W., & Ezzat, S. (2017). Pituitary acromegaly: Not one disease. Endocrine-Related Cancer, 24, C1–C4.

    Article  Google Scholar 

  • Denes, J., Kasuki, L., Trivellin, G., Colli, L. M., Takiya, C. M., Stiles, C. E., et al. (2015). Regulation of aryl hydrocarbon receptor interacting protein (AIP) protein expression by MiR-34a in sporadic somatotropinomas. PLoS One, 10, e0117107.

    Article  Google Scholar 

  • Ezzat, S., Caspar-Bell, G. M., Chik, C. L., Denis, M. C., Domingue, M. E., Imran, S. A., et al. (2019). Predictive markers for postsurgical medical management of acromegaly: A systematic review and consensus treatment guideline. Endocrine Practice, 25, 379–393.

    Article  Google Scholar 

  • Mete, O., Cintosun, A., Pressman, I., & Asa, S. L. (2018). Epidemiology and biomarker profile of pituitary adenohypophysial tumors. Modern Pathology, 31, 900–909.

    Article  CAS  Google Scholar 

  • Spada, A., Arosio, M., Bochicchio, D., Bazzoni, N., Vallar, L., Bassetti, M., et al. (1990). Clinical, biochemical and morphological correlates in patients bearing growth hormone-secreting pituitary tumors with or without constitutively active adenylyl cyclase. The Journal of Clinical Endocrinology and Metabolism, 71, 1421–1426.

    Article  CAS  Google Scholar 

  • Vierimaa, O., Georgitsi, M., Lehtonen, R., Vahteristo, P., Kokko, A., Raitila, A., et al. (2006). Pituitary adenoma predisposition caused by germline mutations in the AIP gene. Science, 312, 1228–1230.

    Article  CAS  Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to Sylvia L. Asa .

Editor information

Editors and Affiliations

Rights and permissions

Reprints and permissions

Copyright information

© 2020 Springer Nature Switzerland AG

About this entry

Check for updates. Verify currency and authenticity via CrossMark

Cite this entry

Asa, S.L. (2020). Somatotroph Tumor. In: van Krieken, J. (eds) Encyclopedia of Pathology. Encyclopedia of Pathology. Springer, Cham. https://doi.org/10.1007/978-3-319-28845-1_5053-1

Download citation

  • DOI: https://doi.org/10.1007/978-3-319-28845-1_5053-1

  • Received:

  • Accepted:

  • Published:

  • Publisher Name: Springer, Cham

  • Print ISBN: 978-3-319-28845-1

  • Online ISBN: 978-3-319-28845-1

  • eBook Packages: Springer Reference MedicineReference Module Medicine

Publish with us

Policies and ethics