Thyroid cancer is an uncommon type of cancer, accounting less than 1% of all cancers in adults, and 0.5-3% of all cancers in children. There are four different types: papillary carcinoma (80-90% of cases), follicular (5-10%), medullary (5%) and anaplastic cell (2-3%). Eighty per cent of cases of medullary thyroid cancer are sporadic, but 20% are associated with an inherited syndrome that is divided into three groups: multiple endocrine neoplasia type 1, multiple endocrine neoplasia type 2 and familial medullary thyroid carcinoma. The inherited forms are caused by a disruption in the RET oncogene, which is located in the long arm of chromosome 10. A hereditary case of medullary thyroid carcinoma is presented. It was detected because of a familial genetic study. The purpose of the paper is emphasize the importance of the early diagnosis and the intervention of multidisciplinary teams of experts.
CITATION STYLE
Herrador, L. M., De Arriba, A., Miguel, G., Ferrer, M., & Labarta, J. I. (2016). Study of Medullary Thyroid Carcinoma from a proband. Archivos Argentinos de Pediatria, 114(6), e421–e424. https://doi.org/10.5546/aap.2016.e421
Mendeley helps you to discover research relevant for your work.