Matrone Antonio, Torregrossa Liborio, Sensi Elisa, Cappellani Daniele, Baronti Walter, Ciampi Raffaele, Molinaro Eleonora, Ugolini Clara, Aghababyan Aleksandr, De Napoli Luigi, Latrofa Francesco, Materazzi Gabriele, Basolo Fulvio, Vitti Paolo, Elisei Rossella
Unit of Endocrinology, Department of Clinical and Experimental Medicine, Pisa University Hospital, Pisa, Italy.
Anatomic Pathology Section, Department of Surgical, Medical, Molecular Pathology and Critical Area, Pisa University Hospital, Pisa, Italy.
Front Oncol. 2019 Dec 17;9:1390. doi: 10.3389/fonc.2019.01390. eCollection 2019.
The diagnosis of the primary origin of metastases to the thyroid gland is not easy, in particular in case of concomitant lung adenocarcinoma which shares several immunophenotypical features. Although rare, these tumors should be completely characterized in order to set up specific therapies. This is the case of a 64-years-old woman referred to our institution for a very advanced neoplastic disease diagnosed both as poorly differentiated/anaplastic thyroid cancer (PDTC/ATC) for the huge involvement of the neck and concomitant lung adenocarcinoma (LA). Neither the clinical features and the imaging evaluation nor the tumor markers allowed a well-defined diagnosis. Moreover, the histologic features of the thyroid and lung biopsies confirmed the synchronous occurrence of two different tumors. The molecular analysis showed a c.34G>T (p.G12C) mutation in the codon 12 of K-RAS gene, in both tissues. Since, this mutation is highly prevalent in LA and virtually absent in PDTC/ATC the lung origin of the malignancy was assumed, and the patient was addressed to the correct therapeutic strategy.
诊断转移至甲状腺的原发肿瘤并不容易,尤其是在伴有具有多种免疫表型特征的肺腺癌的情况下。尽管此类肿瘤罕见,但仍应对其进行全面特征分析,以便制定特定的治疗方案。本文报道了一名64岁女性患者,因颈部广泛受累且伴有肺腺癌(LA),被诊断为低分化/未分化甲状腺癌(PDTC/ATC),病情已发展至晚期,遂转诊至我院。临床特征、影像学评估及肿瘤标志物均无法明确诊断。此外,甲状腺和肺活检的组织学特征证实了两种不同肿瘤的同时存在。分子分析显示,两个组织中的K-RAS基因第12密码子均存在c.34G>T(p.G12C)突变。由于该突变在LA中高度常见,而在PDTC/ATC中几乎不存在,因此推测恶性肿瘤起源于肺部,并为患者制定了正确的治疗策略。