Recurrent parathyromatosis in a patient with concomitant MEN1 and CASR gene alterations: Clinical management of a case report and literature review

INTRODUCTION: Parathyromatosis is a rare cause of primitive hyperparathyroidism characterized by the presence of numerous parathyroid tissue foci in the neck/mediastinum, due to hyperplasia of parathyroid embryologic residues (primary-form) or to local parathyroid tissue implantation (secondary-form...

Descripción completa

Detalles Bibliográficos
Autores principales: Sapuppo, Giulia, Giusti, Maria Ausilia, Aricò, Demetrio, Masucci, Romilda, Tavarelli, Martina, Russo, Marco, Pellegriti, Gabriella
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2023
Materias:
Endocrinology
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10044612/
https://www.ncbi.nlm.nih.gov/pubmed/36998475
http://dx.doi.org/10.3389/fendo.2023.1108278

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10044612/
https://www.ncbi.nlm.nih.gov/pubmed/36998475
http://dx.doi.org/10.3389/fendo.2023.1108278

Ejemplares similares