3P association (3PAs): Pituitary adenoma and pheochromocytoma/paraganglioma. A heterogeneous clinical syndrome associated with different gene mutations
Author:
Funder
Instituto de Salud Carlos III
Georgina Petropoulos Nouna
Instituto de Salud Carlos III (ISCIII), Acción Estratégica en Salud
Publisher
Elsevier BV
Subject
Internal Medicine
Reference46 articles.
1. Clinical practice guidelines for multiple endocrine neoplasia type 1 (MEN1);Thakker;J Clin Endocrinol Metab,2012
2. Multiple endocrine neoplasia;Stewart,2016
3. Pituitary adenoma with paraganglioma/ pheochromocytoma (3PAs) and succinate dehydrogenase defects in humans and mice;Xekouki;J Clin Endocrinol Metab,2015
4. 15 years of paraganglioma: the association of pituitary adenomas and phaeochromocytomas or paragangliomas;O'Toole;Endocr Relat Cancer,2015
5. Case report of a prolactinoma in a patient with a novel MAX mutation and bilateral pheochromocytoma;Roszko;J Endocr Soc,2017
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1. A rare association of pheochromocytoma, paraganglioma, and pituitary adenoma (3PA): A case report and literature review;Medicine;2024-08-09
2. An aggressive cabergoline-resistant, temozolomide-responsive macroprolactinoma due to a germline SDHB pathogenic variant in the absence of paraganglioma or pheochromocytoma;Frontiers in Endocrinology;2023-12-13
3. Rare forms of hereditary endocrine neoplasia: co-existence of pituitary adenoma and pheochromocytoma/paraganglioma;Problems of Endocrinology;2023-05-11
4. Pituitary Tumorigenesis—Implications for Management;Medicina;2023-04-21
5. Succinate dehydrogenase and MYC-associated factor X mutations in pituitary neuroendocrine tumours;Endocrine-Related Cancer;2022-10-01
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