Pheochromocytoma, paragangliomas, and pituitary adenoma: An unusual association in a patient with an SDHD mutation. Case report

RATIONALE: Pituitary adenomas and paragangliomas are both rare endocrine diseases. Paragangliomas (PGL)/pheochromocytomas (PHEO) are part of an inherited syndrome in about 30% to 40% of cases. Among familial cases, mutations of the succinate dehydrogenase (SDH) subunit genes (succinate dehydrogenase...

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Detalles Bibliográficos
Autores principales: Lemelin, Annie, Lapoirie, Marion, Abeillon, Juliette, Lasolle, Hélène, Giraud, Sophie, Philouze, Pierre, Ceruse, Philippe, Raverot, Gérald, Vighetto, Alain, Borson-Chazot, Françoise
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Wolters Kluwer Health 2019
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6708967/
https://www.ncbi.nlm.nih.gov/pubmed/31348302
http://dx.doi.org/10.1097/MD.0000000000016594

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6708967/
https://www.ncbi.nlm.nih.gov/pubmed/31348302
http://dx.doi.org/10.1097/MD.0000000000016594

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