原发性甲状腺平滑肌肉瘤-一种罕见的恶性肿瘤。

Q2 Medicine European Endocrinology Pub Date : 2019-04-01 Epub Date: 2019-04-12 DOI:10.17925/EE.2019.15.1.44
Bhasker Reddy, Vivek Aggarwal, Ajay Kumar Ajmani, Seema Sachan, Deepak Khandelwal
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引用次数: 6

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,多见于老年患者。这些肿瘤的特点是颈部快速生长的肿块,术前难以诊断,尽管进行了根治性手术、化疗和放疗,但其侵袭性很强,复发率很高。我们在此报告一例50岁的女性与快速增长的无痛肿块在颈部。行甲状腺全切除术及双侧颈部淋巴结清扫。组织学和免疫组化检查显示原发性甲状腺LMS。根治性手术后1个月内局部复发。原发性LMS的诊断是困难的,免疫组化是必要的,以区分与其他恶性甲状腺肿瘤。原发性LMS仍然是一种危及生命的肿瘤,需要更有效的治疗来改善预后。
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Primary Leiomyosarcoma of the Thyroid Gland - A Rare Malignancy.

Primary leiomyosarcoma (LMS) of thyroid is rare malignant neoplasm usually seen in elderly patients. These tumours are characterised by a rapidly growing mass in the neck, difficult to diagnose preoperatively and are highly aggressive with high recurrence rates in spite of radical surgery, chemotherapy and radiotherapy. We herein report a case of 50-year-old female with a rapidly growing painless mass in the neck. Total thyroidectomy with bilateral neck node clearance was done. Histology and Immunohistochemistry revealed primary LMS of thyroid gland. Within 1 month of radical surgery she developed local recurrence. Diagnosis of primary LMS is difficult and immunohistochemistry is necessary to differentiate it from other malignancies of the thyroid. Primary LMS remains a life-threatening tumour and more effective treatment are needed to improve outcome.

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European Endocrinology
European Endocrinology Medicine-Endocrinology, Diabetes and Metabolism
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