Child With Ret Proto-Oncogene Codon 634 Mutation
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Date
2017
Authors
Mutafoğlu, Kamer
Journal Title
Journal ISSN
Volume Title
Publisher
Turkish J Pediatrics
Open Access Color
GOLD
Green Open Access
No
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OpenAIRE Views
Publicly Funded
No
Abstract
Herein we reported a 7-year-old child with RET proto-oncogene c634 mutation. Her mother had been diagnosed with medullary thyroid carcinoma (MTC), and treated six years ago. Heterozygous mutation of the RET proto-oncogene at c634 had been detected in her mother. Genetic analysis showed the presence of the same mutation in our patient. Thyroid functions were normal. Serum calcitonin level was found mildly elevated. Parathormone (PTH) and carcinoembrionic antigen (CEA) levels were normal. Prophylactic thyroidectomy and sampling of cervical lymph nodes were performed. Histopathologic examination revealed hyperplasia in thyroid C cells, and reactive lymphadenopathy. The risk of MTC has been reported 100% through the life of patients with RET protooncogene mutation. It has been reported that particularly patients with c634 mutation have more risk of occurence of metastatic and progressive/recurrent MTC. Prophylactic thyroidectomy, cervical lymph node dissection before 5-years-of-age should be considered for these patients.
Description
Keywords
medullary C cell hyperplasia, RET proto-oncogene mutation, prophylactic thyroidectomy, Medullary-Thyroid Carcinoma, Management, Guidelines, Calcitonin, Heterozygote, Proto-Oncogene Proteins c-ret, Thyroid Gland, Pediatrics, Proto-Oncogene Mas, RJ1-570, Carcinoma, Neuroendocrine, RET proto-oncogene mutation, prophylactic thyroidectomy, Mutation, Thyroidectomy, Humans, Female, Genetic Testing, Thyroid Neoplasms, Child, Codon, medullary C cell hyperplasia
Fields of Science
0301 basic medicine, 03 medical and health sciences, 0302 clinical medicine
Citation
WoS Q
Q3
Scopus Q
Q3

OpenCitations Citation Count
1
Source
Turkısh Journal of Pedıatrıcs
Volume
59
Issue
5
Start Page
590
End Page
593
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Citations
CrossRef : 1
Scopus : 1
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Mendeley Readers : 13
SCOPUS™ Citations
1
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Web of Science™ Citations
1
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2
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6
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