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具有 Hurthle 和印戒细胞分化的分化型甲状腺癌的腋窝淋巴结转移。一例具有特殊组织学表现的播散性甲状腺癌。

Axillary node metastasis from differentiated thyroid carcinoma with Hürthle and signet ring cell differentiation. A case of disseminated thyroid cancer with peculiar histologic findings.

机构信息

Thyroid and Parathyroid Surgery Unit, Istituto Nazionale per lo Studio e la Cura dei Tumori, Fondazione G. Pascale, Naples, Italy.

出版信息

BMC Cancer. 2012 Feb 3;12:55. doi: 10.1186/1471-2407-12-55.

Abstract

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.

摘要

背景

分化型甲状腺癌通常与良好的预后和惰性病程相关。远处转移在甲状腺癌发病初期较为罕见。在这些表现中,腋窝淋巴结转移更为罕见:文献中以前仅报道过少数几例病例;尚无甲状腺滤泡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,我们报告了一例播散性分化型甲状腺癌伴腋窝淋巴结转移的病例。患者接受了近全甲状腺切除术和颈部及腋窝淋巴结清扫术。组织病理学诊断为具有“印戒细胞”和 Hurthle 细胞特征的低分化滤泡癌。患者接受了放射性碘治疗和 TSH 抑制治疗。随后,他的血清甲状腺球蛋白水平从 100000ng/ml 以上降至 44000ng/ml。

讨论与结论

目前仅有少数几例甲状腺癌腋窝淋巴结转移的报道,据我们所知,这是首例甲状腺滤泡癌腋窝淋巴结转移的报道。“印戒细胞”是良性和更罕见的恶性滤泡性甲状腺肿瘤共有的形态学特征,通常与滤泡生成停滞相关。我们的病例是迄今为止描述的罕见“印戒细胞”癌之一。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/89aa/3292488/288c393db02e/1471-2407-12-55-1.jpg

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