Carcinoma medular de tiroides metastásico en mama en una paciente con diagnóstico clínico de neoplasia endocrina múltiple subtipo 2B: reporte de un caso
Lorenzo D’Angelo-Piaggio , Jose Echecopar-Sabogal , Diego M. Chanamé-Baca , Alberto Teruya-Gibu
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Abstract
The medullary thyroid carcinoma (MTC) is an unusual malignant neoplasm with a high rate of metastasis. It usually appears as a single nodule in more than 70% of the cases, and the main distant metastasis sites are liver, lung, and bone. Breast metastasis is rare because within the mammary tumours only between 0.2% and 1.3% are secondary tumours. MTC is strongly associated with the multiple endocrine neoplasia sub-type 2B (MEN2B), which is a dominant autosomal disorder characterised by the presence of MTC and phaeochromocytoma in the absence of hyperparathyroidism. Metastasis from a MTC to the breast in the context of a MEN2B rarely occurs, which is why this case is being reported.