ea0065p294 | Neuroendocrinology | SFEBES2019
Abeyaratne Dayakshi
, Gunatilake Sonali
, Joseph Naveen
, Korbonits Marta
, Somasundaram Noel
Background: Pituitary carcinoma is extremely rare and constitute only 0.1−0.2% of all pituitary tumors. Diagnosis is on evidence of metastasis, although these criteria has been challenged. Majority of pituitary carcinomas are functioning tumours, usually secreting ACTH (42%) or prolactin (33%). Common sites of metastasis include the brain, spinal cord, leptomeninges, bone, liver, lymph nodes and lung. Mean survival after detection of metastasis is around 1−2 years....