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Simultaneous Papillary and Medullary Carcinoma in the Thyroid Gland

机译:甲状腺同时发生的乳头状和髓样癌

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Introduction: The most common type of thyroid cancers is papillary thyroid carcinoma originating from follicular cells. Medullar thyroid cancer (MTK), a neuroendocrine tumor, is derived from thyroid parafollicular (C cells) cells. These two carcinomas, which incidences, origins of cells, histopathological features and prognosis are completely different, are rarely found together in the thyroid gland. Case Report: A 55-year-old male patient without a known disease other than COPD, had no history of prior radiation to the head or neck and no known family history of any endocrine disease whose on The pathology of the specimen detected a papillary carcinoma oncocytic variant with a tumor size of 7x5.5x5 cm in the left lobe and a medullary microcarcinoma with a tumor diameter of 2 mm in the right lobe. In immunohistochemical studies; CEA, calcitonin, chromogranin, synaptophysin were positivite and cytokeratin 19 was focal positive. Vascular invasion, perineural invasion, penetration into the thyroid and invasion of soft tissue outside the thyroid were not observed in the pathological examination of both tumors. Postoperative RAI treatment and TSH suppressive treatment were performed on patient. In the scan after RAI treatment, no metastases were detected. Urine vanillyl mandelic acid, 5 hydroxy indole acetic acid and catecholamine levels were normal. Mutation was not detected in the selected exon sequence analysis of RET-protooncogen. Discussion: There is a case report in the literature about the existence of RET and BRAF gene mutations in these simultaneous malignancies. RET proto-oncogen mutation detected in hereditary medullary carcinoma cases has also been reported in some papillary carcinoma cases. Therefore, the appearance of these two tumors at the same time suggests that is linked to RET proto-oncogen mutation. Additional studies are necessary to describe the clinical and pathologic characteristics of these patients and to clarify otential biologic relationship between concurrent medullary thyroid carcinoma and papillary thyroid carcinoma.
机译:简介:最常见的甲状腺癌类型是源自滤泡细胞的乳头状甲状腺癌。甲状腺髓样癌(MTK)是一种神经内分泌肿瘤,来源于甲状腺滤泡旁(C细胞)细胞。这两种癌的发病率,细胞起源,组织病理学特征和预后完全不同,在甲状腺中很少发现。病例报告:一名55岁的男性患者,除COPD以外,无其他已知疾病,无先前对头部或颈部的放射史,也无任何内分泌性疾病的家族史,该内分泌性疾病的标本在病理学上发现了乳头状癌左叶肿瘤大小为7x5.5x5 cm的胞浆变种,右叶肿瘤大小为2 mm的髓样微癌。在免疫组化研究中; CEA,降钙素,嗜铬粒蛋白,突触素为阳性,而细胞角蛋白19为局灶性阳性。在两种肿瘤的病理学检查中均未观察到血管浸润,神经周围浸润,穿透甲状腺和甲状腺外软组织的浸润。对患者进行术后RAI治疗和TSH抑制治疗。在RAI治疗后的扫描中,未发现转移。尿液香草基扁桃酸,5-羟基吲哚乙酸和儿茶酚胺水平正常。在RET原癌基因的所选外显子序列分析中未检测到突变。讨论:文献中有一个病例报告涉及这些同时发生的恶性肿瘤中RET和BRAF基因突变的存在。在一些乳头状癌病例中也已报道了在遗传性髓样癌病例中检测到的RET原癌基因突变。因此,这两个肿瘤同时出现提示与RET原癌基因突变有关。需要进一步的研究来描述这些患者的临床和病理特征,并阐明并发甲状腺髓样癌和甲状腺乳头状癌之间的潜在生物学关系。

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