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甲状腺全切除术联合化疗用于原发性甲状腺鳞状细胞癌。

Total thyroidectomy associated to chemotherapy in primary squamous cell carcinoma of the thyroid.

作者信息

De Cesare A, Di Cristofano C, Di Filippo A R, Salesi N, Spaziani M, Picchio M, Spaziani E

机构信息

Department of Surgery, "Pietro Valdoni", Sapienza University of Rome.

Department of Medico-Surgical Sciences and Biotechnologies, Sapienza University of Rome, Polo Pontino, Terracina, Latina.

出版信息

Clin Ter. 2019 Jul-Aug;170(4):e231-e234. doi: 10.7417/CT.2019.2138.

Abstract

Primary squamous cell carcinoma of the thyroid (PSCCT) is a rare malignant disease with rapid fatal prognosis. The onset is generally characterized by sudden bilateral latero-cervical lymphadenopathy. The Authors report patient of 58-year-old who referred for evaluation of rapidly aggravating bilateral latero-cervical lymphadenopathy. The US highlighted the presence of a hypoechoic nodular lesion characterized by peri and intra-nodular vascularization. Multilayer CT showed diffused involvement of mediastinal and bilateral latero-cervical lymph nodes, with no evidence of primary pulmonary neoplasia or elsewhere. The patient underwent total thyroidectomy. The peri-isthmic tissue was removed due to the presence of a small roundish formation, that was due to lymph node metastasis at histological examination. Histological diagnosis: PSCCT. The immunohistochemical panel of the thyroid lesion was indispensable for the differential diagnosis between PSCCT, medullary carcinoma, anaplastic carcinoma, and thyroid metastasis of neoplasia with unknown primitiveness. The patient underwent chemotherapeutic treatment with Carboplatin and Paclitaxel with modest improvement of dysphagia symptoms and reduction of 10-15% of the target lesions. The clinical course was characterized by loco-regional progression of the disease with exitus in 10 months after diagnosis. Survival and quality of life after surgical therapy and chemotherapy were like that of patients undergoing only chemotherapy. Due to the extreme rarity of the neoplasia, 60 cases described in Literature, no exclusive guidelines are reported for PSCCT. More extensive case studies are needed to evaluate the effects of total thyroidectomy with intent R0/R1 on improving survival and quality of life of patients with PSCCT.

摘要

甲状腺原发性鳞状细胞癌(PSCCT)是一种罕见的恶性疾病,预后迅速致命。发病通常以突发双侧颈侧淋巴结病为特征。作者报告了一名58岁的患者,因迅速加重的双侧颈侧淋巴结病前来评估。超声检查显示存在一个低回声结节性病变,其特征为结节周围和内部有血管形成。多层CT显示纵隔和双侧颈侧淋巴结弥漫性受累,未发现原发性肺肿瘤或其他部位的肿瘤迹象。患者接受了全甲状腺切除术。由于存在一个小圆形结构,峡部周围组织被切除,组织学检查显示这是淋巴结转移。组织学诊断:PSCCT。甲状腺病变的免疫组织化学检测对于PSCCT、髓样癌、未分化癌以及原发部位不明的肿瘤甲状腺转移之间的鉴别诊断是必不可少的。患者接受了卡铂和紫杉醇化疗,吞咽困难症状略有改善,靶病变缩小了10 - 15%。临床病程以疾病局部进展为特征,诊断后10个月死亡。手术治疗和化疗后的生存情况及生活质量与仅接受化疗的患者相似。由于该肿瘤极为罕见,文献中仅描述了60例,目前尚无关于PSCCT的专门指南。需要更广泛的病例研究来评估R0/R1切除范围的全甲状腺切除术对改善PSCCT患者生存和生活质量的影响。

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