Clinical Features
Incidence
Pituitary carcinoma represents around 0.4% of surgically resected adenohypophysial tumors (Alshaikh et al. 2019).
Age
This rare tumor has been reported at any adult age.
Sex
There is no gender predilection.
Site
Pituitary neuroendocrine tumors usually arise in the sella turcica. Metastatic foci that have been reported in pituitary carcinomas include dissemination to multiple cerebrospinal sites, lymph nodes (usually in the neck), liver, lungs, and bone in multiple locations, most commonly spine (Asa and Perry 2020).
Clinical and Biochemical Features
The initial clinical presentation is usually that of a pituitary neuroendocrine tumor; patients have presented with the signs and...
References and Further Reading
Alshaikh, O. M., Asa, S. L., Mete, O., & Ezzat, S. (2019). An institutional experience of tumor progression to pituitary carcinoma in a 15 year cohort of 1055 consecutive pituitary neuroendocrine tumors. Endocrine Pathology, 30(2), 118–127.
Asa, S. L., & Perry, A. (2020). Tumors of the pituitary gland (AFIP atlas of tumor pathology, series 5). Silver Spring: ARP Press.
DeLellis, R. A., Lloyd, R. V., Heitz, P. U., & Eng, C. (2004). Pathology and genetics of tumors of endocrine organs. Lyons: IARC Press.
Lloyd, R. V., Osamura, R. Y., Kloppel, G., & Rosai, J. (2017). WHO classification of tumors of endocrine organs (4th ed.). Lyon: IARC.
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Asa, S.L. (2020). Pituitary Carcinoma. In: van Krieken, J. (eds) Encyclopedia of Pathology. Encyclopedia of Pathology. Springer, Cham. https://doi.org/10.1007/978-3-319-28845-1_5049-1
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DOI: https://doi.org/10.1007/978-3-319-28845-1_5049-1
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