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
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

17588359241265222

Informations de copyright

© The Author(s), 2024.

Déclaration de conflit d'intérêts

The authors declare that there is no conflict of interest.

Auteurs

Ekaterina Kim (E)

Department of the Parathyroid Glands Pathology and Mineral Metabolism Disorders, Endocrinology Research Centre, Dmitriya Ulianova Street, 11, Moscow 117036, Russia.

Natalia Kalinchenko (N)

Children's Department of Thyroidology, Reproductive and Somatic Development, Endocrinology Research Centre, Moscow, Russia.

Anna Eremkina (A)

Department of the Parathyroid Glands Pathology and Mineral Metabolism Disorders, Endocrinology Research Centre, Moscow, Russia.

Liliya Urusova (L)

Department of Fundamental Pathomorphological, Endocrinology Research Centre, Moscow, Russia.

Rustam Salimkhanov (R)

Department of the Parathyroid Glands Pathology and Mineral Metabolism Disorders, Endocrinology Research Centre, Moscow, Russia.

Natalia Mokrysheva (N)

Endocrinology Research Centre, Moscow, Russia.

Classifications MeSH