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首页> 外文期刊>BMC Cancer >Axillary node metastasis from differentiated thyroid carcinoma with hürthle and signet ring cell differentiation. A case of disseminated thyroid cancer with peculiar histologic findings
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Axillary node metastasis from differentiated thyroid carcinoma with hürthle and signet ring cell differentiation. A case of disseminated thyroid cancer with peculiar histologic findings

机译:分化型甲状腺癌伴hürthle和印戒细胞分化引起的腋窝淋巴结转移。一例具有特殊组织学发现的弥漫性甲状腺癌

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Background Differentiated thyroid cancer is usually associated with an excellent prognosis and indolent course. Distant metastases are rare events at the onset of thyroid cancer. Among these presentations, metastasis to the axillary lymph nodes is even more unusual: only few cases were previously reported in the literature; there has been no report of axillary lymph node metastasis from follicular thyroid carcinoma. Axillary lymph node metastasis generally arises in the context of disseminated disease and carries an ominous prognosis. Case presentation Here we present a case of axillary lymph node metastasis in the context of disseminated differentiated thyroid cancer. The patient underwent near total thyroidectomy and neck and axillary lymph node dissection. A histopathological diagnosis of poorly differentiated follicular carcinoma with "signet ring cells" and Hürthle cell features was established. The patient received radioactive iodine therapy and TSH suppression therapy. Subsequently his serum thyroglobulin level decreased to 44.000 ng/ml from over 100.000 ng/ml. Discussion and Conclusion Currently there are only few reported cases of axillary node metastases from thyroid cancer, and to our knowledge, this is the first report on axillary lymph node metastasis from follicular thyroid carcinoma. "Signet ring cell" is a morphologic feature shared by both benign and, more rarely, malignant follicular thyroid neoplasm, and it generally correlates with an arrest in folliculogenesis. Our case is one of the rare "signet ring cells" carcinomas so far described.
机译:背景分化型甲状腺癌通常与良好的预后和顽固的病程有关。远处转移是甲状腺癌发作时的罕见事件。在这些表现中,腋窝淋巴结转移更为罕见:以前文献报道的病例很少;尚无关于滤泡性甲状腺癌腋窝淋巴结转移的报道。腋窝淋巴结转移通常发生在播散性疾病的背景下,预后不良。病例介绍在这里,我们介绍了在弥漫性分化型甲状腺癌的背景下腋窝淋巴结转移的病例。该患者接受了近全甲状腺切除术以及颈部和腋窝淋巴结清扫术。建立了具有“印戒细胞”和Hürthle细胞特征的低分化滤泡癌的组织病理学诊断。患者接受了放射性碘疗法和TSH抑制疗法。随后,他的血清甲状腺球蛋白水平从超过100.000 ng / ml降至44.000 ng / ml。讨论与结论当前,只有少数报道的甲状腺癌腋窝淋巴结转移病例报道,据我们所知,这是关于滤泡性甲状腺癌腋窝淋巴结转移的首例报道。 “印戒细胞”是良性的(更常见的是恶性的)滤泡性甲状腺肿瘤所共有的一种形态学特征,通常与滤泡发生的停止有关。我们的病例是迄今为止描述的罕见的“印戒细胞”癌之一。

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