原发性乳头状癌起源于鳃裂囊肿。

Jin Seong Cho, Sun Hyoung Shin, Hee Kyung Kim, Ji Shin Lee, Min Ho Park, Jung Han Yoon, Young Jong Jegal
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引用次数: 10

摘要

虽然鳃裂囊肿很常见,但由其引起的乳头状癌却很少见。我们在此报告一位41岁的女性,她的乳头状癌起源于右侧鳃裂囊肿,没有任何甲状腺乳头状癌的证据。患者行右侧颈外侧清扫术后行甲状腺全切除术。然后,我们通过甲状腺球蛋白(TG)、甲状腺相关转录因子-1 (TTF-1)和p63的显微镜和免疫组织化学染色证实了鳃裂囊肿引起的乳头状癌。这是全球第10例描述鳃裂囊肿乳头状癌的病例,我们回顾了有关该病特征的文献,并讨论了TG、TTF -1和p63免疫组化染色的作用。总之,应该强调的是,外科医生必须警惕鳃裂囊肿原发性乳头状癌的可能性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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Primary papillary carcinoma originated from a branchial cleft cyst.

Although branchial cleft cysts are common, papillary carcinomas arising from them are rare. Here we report a 41-year-old woman with papillary carcinoma originating from a right lateral branchial cleft cyst without any evidence of a papillary carcinoma in the thyroid gland. The patient underwent right lateral neck dissection followed by total thyroidectomy. We then confirmed papillary carcinoma arising from the branchial cleft cyst through microscopic and immunohistochemical staining with thyroglobulin (TG), thyroid-associated transcription factor-1 (TTF-1) and p63. It is the 10th case worldwide describing papillary carcinoma in a branchial cleft cyst with a review of the literature on the features of the disease and discussion of the role of immunohistochemical staining with TG, TTF -1 and p63. In conclusion, it should be emphasized that the surgeon must be cautioned of the possibility of primary papillary carcinoma in the branchial cleft cyst.

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