SAT-LB066 Clinical Characteristics of Incidentally Discovered Functioning Adrenal Tumors: Study of Advancing Care and Pathogenesis of Intractable Adrenal Diseases in Japan (ACPA-J)

Objectives: Pheochromocytoma and paraganglioma (PPGL), Cushing syndrome (CS), bilateral macronodular adrenal hyperplasia (BMAH) and adrenocortical carcinoma (ACC) are rare adrenal tumors. Hence, collaboration of researchers and clinicians from several institutes and constructing patient registry are...

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Detalles Bibliográficos
Autores principales: Tanabe, Akiyo, Naruse, Mitsuhide, Katabami, Takuyuki, Izawa, Shoichiro, Yoshimoto, Takanobu, Otsuki, Michio, Sone, Masakatsu, Takeda, Yoshiyu, Okamura, Shintaro, Ichijo, Takamasa
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Endocrine Society 2019
Materias:
Adrenal
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6551719/
http://dx.doi.org/10.1210/js.2019-SAT-LB066

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6551719/
http://dx.doi.org/10.1210/js.2019-SAT-LB066

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