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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...

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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

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