Synonyms
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...
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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.
Asa, S. L., Kucharczyk, W., & Ezzat, S. (2017). Pituitary acromegaly: Not one disease. Endocrine-Related Cancer, 24, C1–C4.
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.
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.
Mete, O., Cintosun, A., Pressman, I., & Asa, S. L. (2018). Epidemiology and biomarker profile of pituitary adenohypophysial tumors. Modern Pathology, 31, 900–909.
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.
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.
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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
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DOI: https://doi.org/10.1007/978-3-319-28845-1_5053-1
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