A rare germline mutation c.2752 A>G (p.M918V) in the RET protooncogene in a patient with medullary and papillary thyroid carcinomas in cervical lymph node metastases: a case report and review of the literature

A rare germline mutation c.2752 A>G (p.M918V) in the RET protooncogene in a patient with medullary and papillary thyroid carcinomas in cervical lymph node metastases: a case report and review of the literature

We report a rare germline RET mutation c.2752 AG (p.M918V) found in a 62-year-old man with synchronous medullary thyroid carcinoma (MTC) and papillary thyroid carcinoma (PTC) (follicular variant) in cervical lymph node metastases with significant predominance of MTC. DNA sequencing of six exons (10,...

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Bibliographic Details
Main Authors: Faina A. Amosenko, Vladimir V. Khvostovoy, Olga A. Shchagina, Alexandr V. Polyakov
Format: Article
Language:Russian
Published: Endocrinology Research Centre 2016-06-01
Series:Клиническая и экспериментальная тиреоидология
Subjects:
thyroid
medullary carcinoma
papillary carcinoma
concurrent (associated) cancer
germline mutation
protooncogene ret
Online Access:https://cet-endojournals.ru/ket/article/viewFile/7942/5830

Internet

https://cet-endojournals.ru/ket/article/viewFile/7942/5830

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