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甲状腺原发性单相滑膜肉瘤的细胞学特征。

Cytologic features of primary monophasic synovial sarcoma of the thyroid gland.

作者信息

Park Chang-Soo, Kim Young, Jeong Eun-Hui, Kim Nah-Ihm, Choi Yoo-Duk

机构信息

Address: Department of Pathology, Chonnam National University Medical School, Gwangju, Republic of Korea.

Department of Pathology, Yeocheon Chonnam Hospital, Yeocheon, Republic of Korea.

出版信息

Cytojournal. 2017 Oct 12;14:24. doi: 10.4103/cytojournal.cytojournal_14_17. eCollection 2017.

Abstract

Synovial sarcoma (SS) is a rare soft tissue tumor, commonly arising in para-articular areas of extremities, but can also present in the head and neck area. However, primary SS of the thyroid gland is an extremely rare tumor which has been reported only five times in previous English literatures. This report presents fine needle aspiration (FNA) cytology of primary monophasic SS of the thyroid gland. A 47-year- old woman incidentally detected thyroid nodule in the isthmus of right thyroid gland on an ultrasonography by regular health check-up. Because the possibility of malignancy could not be ruled out, FNA and surgical resection were performed. The cytological, histopathological, immunohistochemical, and molecular genetic study of SYT-SSX transcript were discussed. For the past 3 years of follow-up after surgery, no recurrence or metastasis has been identified.

摘要

滑膜肉瘤(SS)是一种罕见的软组织肿瘤,通常发生于四肢关节旁区域,但也可出现在头颈部。然而,甲状腺原发性滑膜肉瘤是一种极其罕见的肿瘤,此前英文文献仅报道过5例。本文报告了1例甲状腺原发性单相滑膜肉瘤的细针穿刺(FNA)细胞学检查结果。一名47岁女性在定期健康检查的超声检查中偶然发现右甲状腺峡部有甲状腺结节。由于不能排除恶性可能性,遂进行了FNA及手术切除。文中讨论了SYT-SSX转录本的细胞学、组织病理学、免疫组织化学及分子遗传学研究。术后3年随访未发现复发或转移。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/69d9/5721497/3bd8ed5ceb12/CJ-14-24-g001.jpg

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