原发性甲状腺平滑肌肉瘤1例报告并文献复习

Cherry Tj, R Tasevski, R. Li
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摘要

摘要原发性甲状腺平滑肌肉瘤是一种罕见的恶性肿瘤。患者通常表现为疾病晚期,不到10%的患者存活超过一年。在诊断时,很难从细胞学上区分梭形细胞恶性肿瘤。我们报告一位66岁的男性患者,他需要切开活检来获得甲状腺平滑肌肉瘤的诊断,并允许适当的治疗。*通信:Tiffany Cherry,澳大利亚维多利亚州帕克维尔格拉坦街皇家墨尔本医院普通外科,E-mail: Tiffany。cherry@mh.org.au
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Primary thyroid leiomyosarcoma - case report and literature review
Primary thyroid leiomyosarcoma is a rare malignancy. Patients usually present with advanced disease and less than 10% survive beyond one year. In making the diagnosis it is difficult to distinguish cytologically between spindle cell malignancies. We present a 66-year old male patient who required open incisional biopsy to obtain the diagnosis of thyroid leiomyosarcoma and allow for appropriate management. *Correspondence to: Tiffany Cherry, Department of General Surgery, Royal Melbourne Hospital, Grattan St, Parkville, VIC, Australia, E-mail: tiffany. cherry@mh.org.au
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