Cargando…
Papillary Thyroid Carcinoma and Cushing’s Disease: A Rare Association With Multiple Endocrine Neoplasia Type 1
Introduction: Multiple Endocrine Neoplasia type 1 (MEN1) is characterized by tumours of the parathyroid glands, neuroendocrine pancreatic tumour (PNET), and anterior pituitary. Studies suggest that MEN1 gen is not etiologically related to the oncogenesis of the papillary thyroid carcinoma (PTC). Exp...
Autores principales: | Benevides, Léo Nunes, Holanda, Pedro Gomes Pinto, de Melo, Aline Teixeira, Pinheiro, Juliana Tomaz, Soares, Carlos Eduardo Lopes, Alencar, Renata Carvalho, Martins, Manoel R A, Lourenco, Delmar Muniz, Quidute, Ana Rosa |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2021
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8089161/ http://dx.doi.org/10.1210/jendso/bvab048.2052 |
Ejemplares similares
-
Comparative Analysis of Different International Criteria (ACMG-AMP vs. TENGEN) Applied to Classification of Missense Germline Allelic Variants in Patients With Multiple Endocrine Neoplasia Type 1 or Suspected to this Syndrome
por: Lugeiro, Palloma C, et al.
Publicado: (2021) -
Giant Prolactinoma Causing Hydrocephalus and Intracranial Hypertension as First Manifestations of Multiple Endocrine Neoplasia Type 1
por: Dantas, Naiara C. B., et al.
Publicado: (2019) -
Comprehensive Analysis of Clinical Features in Index Cases With Multiple Endocrine Neoplasia Type 1 Refine the Risk Rate for Detection of Mutation Distinguishing Negative-Mutation (Phenocopies) and Positive-Mutation Cases
por: Urtremari, Betsaida, et al.
Publicado: (2021) -
Recurrent Pheochromocytoma, as Component of Multiple Endocrine Neoplasia
por: Dominguez, Hydelene Beray, et al.
Publicado: (2021) -
SUN-938 Rare Case of Ectopic Cushing Syndrome Caused by ACTH Secreting Thymic Neuroendocrine Tumor in a Patient with Multiple Endocrine Neoplasia Type 1
por: Gorantla, Yamuna, et al.
Publicado: (2020)