Carcinoma medular de tiroides metastásico en mama en una paciente con diagnóstico clínico de neoplasia endocrina múltiple subtipo 2B: reporte de un caso

IF 0.1 Q4 ONCOLOGY Gaceta Mexicana de Oncologia Pub Date : 2016-07-01 DOI:10.1016/j.gamo.2016.07.001
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.

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临床诊断为多发性内分泌肿瘤亚型2B的乳腺癌转移性甲状腺髓样癌:一例报告
甲状腺髓样癌(MTC)是一种罕见的恶性肿瘤,具有很高的转移率。在70%以上的病例中,它通常表现为单个结节,主要的远处转移部位是肝、肺和骨。乳腺转移是罕见的,因为在乳腺肿瘤中只有0.2%至1.3%是继发性肿瘤。MTC与多发性内分泌瘤亚型2B (MEN2B)密切相关,MEN2B是一种显性常染色体疾病,其特征是在没有甲状旁腺功能亢进的情况下存在MTC和嗜铬细胞瘤。在MEN2B的背景下,从MTC转移到乳房的情况很少发生,这就是为什么本病例被报道的原因。
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