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.

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

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