The 3Pas: an update on the association of pheochromocytomas, paragangliomas and pituitary tumours
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Authors
Xekouki, Paraskevi
Brennand, Ana
Whitelaw, Ben
Pacak, Karel
Stratakis, Constantine A.
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Issue Date
2019
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Article
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Abstract
Pituitary adenomas (PA) and pheochromocytomas/paragangliomas (PHEO/PGL) are rare tumors. Although they may co-exist by coincidence, there is mounting evidence that genes predisposing in PHEO/PGL development, may play a role in pituitary tumorigenesis. In 2012, we described a GH-secreting PA caused by an
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Journal
Hormone and Metabolic Research
Volume
51
Issue
07
