Distribution of RET Mutations and Evaluation of Treatment Approaches in Hereditary Medullary Thyroid Carcinoma in Turkey
JOURNAL OF CLINICAL RESEARCH IN PEDIATRIC ENDOCRINOLOGY, vol.8, no.1, pp.13-20, 2016 (SCI-Expanded, Scopus, TRDizin)
- Publication Type: Article / Article
- Volume: 8 Issue: 1
- Publication Date: 2016
- Doi Number: 10.4274/jcrpe.2219
- Journal Name: JOURNAL OF CLINICAL RESEARCH IN PEDIATRIC ENDOCRINOLOGY
- Journal Indexes: Science Citation Index Expanded (SCI-EXPANDED), Scopus, TR DİZİN (ULAKBİM)
- Page Numbers: pp.13-20
- Keywords: Sporadic medullary thyroid carcinoma, hereditary medullary thyroid carcinoma, multiple endocrine neoplasia, RET mutation, ENDOCRINE NEOPLASIA TYPE-2, PROTOONCOGENE MUTATIONS, MEN 2A, PREVALENCE, FAMILIES, CANCER, GUIDELINES, MANAGEMENT, EXPERIENCE, PHENOTYPE
- Open Archive Collection: AVESIS Open Access Collection
- Hacettepe University Affiliated: Yes
Abstract
Objective: This retrospective multicenter study, centrally conducted and supported by the Society of Endocrinology and Metabolism of Turkey, aimed to evaluate the impact of free RET proto-oncogene testing in medullary thyroid carcinoma (MTC) patients. Surgical timing, adequacy of the treatment, and frequency of prophylactic thyroidectomy (PTx) in mutation carriers were also assessed.