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Metastasis of renal cell carcinoma to the parathyroid gland 16 years after radical nephrectomy: A case report

机译:肾癌根治术后16年肾细胞癌转移至甲状旁腺1例

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摘要

Renal cell carcinoma (RCC) has a high metastatic potential, and most commonly metastasizes via the bloodstream, although lymphatic metastases also occur. RCC is well-known for its propensity to metastasize to unusual sites, and late metastasis, even after a number of years, is common. The occurrence of RCC metastasis to the head and neck region is uncommon, and occurs primarily in the thyroid gland and in patients with widespread dissemination. Involvement of the parathyroid gland in metastatic carcinoma is extremely rare. In the present report, a case of metastasis confined to the parathyroid gland is described, likely with intrathyroidal localization, arising from a RCC that occurred 16 years after nephrectomy. A 66-year-old man was referred to the Department of Surgery of the University Hospital of Pisa (Pisa, Italy) with a preoperative fine-needle aspiration diagnosis of a follicular lesion in the context of nodular goiter of the thyroid gland. The previous medical history of the patient included a right nephrectomy for the treatment of clear cell RCC in February 1997. No other distant metastases were identified as of the latest follow-up in March 2014. At the time of thyroid surgery, the thyroid and parathyroid function tests were normal. The gross appearance of the surgical specimen was a multinodular goiter with a solid nodule measuring 33 mm on the left lobe of the thyroid gland. Microscopic examination revealed a completely encapsulated lesion consisting of clear cells arranged in a solid pattern and intermixed with fragments of parathyroid tissue. Following immunohistochemical examination, the clear cell lesion was negative for thyroid transcription factor-1 and thyroglobulin and strongly positive for epithelial membrane antigen, cluster of differentiation 10 and vimentin. To the best of our knowledge, this is the second case of metastasis to the parathyroid gland from a RCC reported in the literature.
机译:肾细胞癌(RCC)具有很高的转移潜能,尽管也发生淋巴转移,但最常见的转移途径是通过血流。 RCC以转移到异常部位的倾向而闻名,即使数年后,晚期转移也很普遍。 RCC转移至头颈部区域的情况很少见,主要发生在甲状腺和广泛分布的患者中。甲状旁腺累及转移性癌极为罕见。在本报告中,描述了仅局限于甲状旁腺的转移病例,可能是由于肾切除术后16年发生的RCC而引起的甲状腺内定位。一名66岁的男子被转诊至比萨大学医院(意大利比萨)的外科,对甲状腺结节性甲状腺肿进行了术前细针穿刺诊断为滤泡性病变。该患者的先前病史包括在1997年2月进行右肾切除术治疗透明细胞RCC。2014年3月的最新随访未发现其他远处转移灶。在进行甲状腺手术时,甲状腺和甲状旁腺功能测试正常。手术标本的总体外观为多结节性甲状腺肿,甲状腺左叶上有一个实心结节,长33毫米。显微镜检查显示完全包封的病变,由透明细胞以实心模式排列并与甲状旁腺组织碎片混合在一起。免疫组织化学检查后,透明细胞病变的甲状腺转录因子-1和甲状腺球蛋白阴性,而上皮膜抗原,分化簇10和波形蛋白强烈阳性。据我们所知,这是文献中报道的第二例从RCC转移至甲状旁腺的病例。

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