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A family of multiple endocrine neoplasia type 2A associated with a C618R mutation in RET proto-oncogene / 대한내과학회지
Korean Journal of Medicine ; : 448-454, 2006.
Artículo en Coreano | WPRIM | ID: wpr-160197
ABSTRACT
Medullary thyroid carcinoma (MTC) is a relatively rare malignant thyroid disease that accounts for approximately 1% to 5% of all thyroid carcinomas. MTC occurs as a sporadic disease and as an inherited disease with the multiple endocrine neoplasia type 2A (MEN2A), MEN2B, and familial non-MEN medullary carcinoma (FMTC). MEN2A is characterized by MTC, pheochromocytoma, and parathyroid adenoma. The mutation of RET proto-oncogene plays an important role in MEN2A syndromes. Recently the authors diagnosed MEN2A patient and screened his family with thyroid ultrasonogram and RET proto-oncogene analysis. A genetic analysis of the peripheral leukocyte showed a codon 618 mutation (Cys618Arg) at exon 10 of the RET proto-oncogene in a family presenting third generations from age 7 to age 56 years. We report this case of MEN2A with a review of the related literatures.
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Texto completo: Disponible Índice: WPRIM (Pacífico Occidental) Asunto principal: Neoplasias de las Paratiroides / Feocromocitoma / Enfermedades de la Tiroides / Glándula Tiroides / Proto-Oncogenes / Codón / Neoplasia Endocrina Múltiple / Neoplasias de la Tiroides / Composición Familiar / Exones Tipo de estudio: Estudio diagnóstico Límite: Humanos Idioma: Coreano Revista: Korean Journal of Medicine Año: 2006 Tipo del documento: Artículo

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Texto completo: Disponible Índice: WPRIM (Pacífico Occidental) Asunto principal: Neoplasias de las Paratiroides / Feocromocitoma / Enfermedades de la Tiroides / Glándula Tiroides / Proto-Oncogenes / Codón / Neoplasia Endocrina Múltiple / Neoplasias de la Tiroides / Composición Familiar / Exones Tipo de estudio: Estudio diagnóstico Límite: Humanos Idioma: Coreano Revista: Korean Journal of Medicine Año: 2006 Tipo del documento: Artículo