Combination approach for
CDC73 mutation
adolescent
case report
parathyroid carcinoma
radiotherapy
Journal
Therapeutic advances in medical oncology
ISSN: 1758-8340
Titre abrégé: Ther Adv Med Oncol
Pays: England
ID NLM: 101510808
Informations de publication
Date de publication:
2024
2024
Historique:
received:
14
12
2023
accepted:
13
06
2024
medline:
5
8
2024
pubmed:
5
8
2024
entrez:
5
8
2024
Statut:
epublish
Résumé
Parathyroid carcinoma (PC) is extremely rare in children and adolescent. PC is more often sporadic, but also it could be associated with germline mutations. The clinical features of primary hyperparathyroidism (PHPT) are nonspecific in children and adolescent, which delays the diagnosis for years. This case of PC in a pediatric patient, caused by germline heterozygous pathogenic variant in exon 1 of the
Identifiants
pubmed: 39099848
doi: 10.1177/17588359241265222
pii: 10.1177_17588359241265222
pmc: PMC11295221
doi:
Types de publication
Case Reports
Journal Article
Langues
eng
Pagination
17588359241265222Informations de copyright
© The Author(s), 2024.
Déclaration de conflit d'intérêts
The authors declare that there is no conflict of interest.