An extremely rare association of TSH-secreting pituitary adenoma, metastatic neuroendocrine tumor and Cushing’s syndrome in a patient with MEN-1 gene mutation

Multiple endocrine neoplasia (MEN)-1 syndrome is a rare disorder, due to the loss of function of the tumor suppressor menin. It consists of the association of two or more endocrine tumors, often presenting in a familial setting, being inherited in an autosomal dominant fashion. The most frequent man...

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Detalhes bibliográficos

Principais autores:	Giuseppe Giuffrida, Erika Messina, Petronilla Daniela Romeo, Adriana Albani, Valeria Barresi, Sergio Baldari, Giuseppe Navarra, Francesco Ferraù, Salvatore Cannavò
Formato:	Artigo
Idioma:	Inglês
Publicado em:	Accademia Peloritana dei Pericolanti 2018-06-01
Colecção:	Atti della Accademia Peloritana dei Pericolanti - Classe di Scienze Medico-Biologiche
Assuntos:	MEN-1 TSH-secreting pituitary adenomas adrenal hyperplasia Cushing’s syndrome hyperparathyroidism
Acesso em linha:	http://cab.unime.it/journals/index.php/APMB/article/view/1853
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