A Case of Medullary Thyroid Carcinoma Combined with Papillary Microcarcinoma and Literature Review

Shasha Liu, Yang Zhao, Xing Zhao
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Abstract

Background: The histologic type of thyroid carcinomas includes follicular, papillary carcinomas, and medullary carcinomas. The reports about the histological, immunohistochemical, and ultrastructural characteristics of each kind of thyroid carcinomas were common, but the simultaneous occurrence of a medullary and papillary carcinoma as 2 distinct tumors has been reported extremely rarely. Objects: To explore the pathogenesis, clinicopathological characteristics, immunohistochemical phenotype, and pathological diagnosis of medullary thyroid carcinoma combined with papillary thyroid microcarcinoma. Methods: The clinicopathological characteristics and immunohistochemical phenotype of a patient with left medullary thyroid carcinoma combined with right papillary thyroid microcarcinoma were retrospectively stu-died. Then, relevant literature was thus reviewed. Results: General appearance: The size of the left thyroid lobe was 2.5 × 2 × 1 cm, the cut surface was gray and red, and a nodule with a diameter of 1.3 cm could be observed. The cut surface of the nodule was gray and yellow, solid, and hard. The size of the right lobe of the thyroid gland was 0.7 × 0.6 × 0.5 cm, and a gray nodule with a diameter of 0.4 cm was seen on the cut surface. The cut surface of the nodule was gray, solid, and hard. Observation under the microscope: the left nodular tumor cells were round, oval, or plasma cell-like, some areas were arranged in nests, and some areas were arranged in beams. Calcification and sheet-like eosinophilic amyloid deposits could be seen in the stroma. The nodule on the right showed a branched papillary structure, the covering cells on the surface of the nipple were ground glass-like nuclei, and nuclear grooves and pseudo-inclusion bodies in the nucleus could be observed. Immunohistochemistry: left lobe tumor cells Calcitonin, CEA, TTF-1, CD56, CgA, and Syn are all (+), CK19 and TG were both (−); right lobe tumor cells CK19 and TG are both (+), Calcitonin, CD56, CgA, and Syn are all (−). Conclusions: The origin, clinicopathological manifestations, and immunophenotypes of medullary thyroid carcinoma and papillary thyroid carcinoma are different. It is relatively rare for the two to occur at the same time. The diagnosis mainly depends on the microscopic morphology and immunophenotype characteristics.
甲状腺髓样癌合并乳头状微癌1例并文献复习
背景:甲状腺癌的组织学类型包括滤泡癌、乳头状癌和髓样癌。各类甲状腺癌的组织学、免疫组织化学及超微结构特征报道较多,但髓样癌和乳头状癌作为两种不同肿瘤同时发生的报道极为罕见。目的:探讨甲状腺髓样癌合并甲状腺乳头状微癌的发病机制、临床病理特点、免疫组织化学表型及病理诊断。方法:回顾性分析1例左甲状腺髓样癌合并右甲状腺乳头状微癌的临床病理特点及免疫组化表型。然后,对相关文献进行综述。结果:一般外观:左侧甲状腺叶大小2.5 × 2 × 1 cm,切面灰红色,可见直径1.3 cm的结节。结节切面灰黄色,实心坚硬。甲状腺右叶大小0.7 × 0.6 × 0.5 cm,切面见一直径0.4 cm的灰色结节。结节切面呈灰色,实心坚硬。镜下观察:左侧结节状肿瘤细胞呈圆形、卵圆形或浆细胞样,部分呈巢状排列,部分呈束状排列。间质可见钙化和片状嗜酸性淀粉样蛋白沉积。右侧结节呈支状乳头状结构,乳头表面覆盖细胞为磨玻璃样核,核内可见核沟和假包涵体。免疫组化:左叶肿瘤细胞降钙素、CEA、TTF-1、CD56、CgA、Syn均为(+),CK19、TG均为(−);右肺肿瘤细胞CK19和TG均为(+),降钙素、CD56、CgA和Syn均为(−)。结论:甲状腺髓样癌与甲状腺乳头状癌的起源、临床病理表现及免疫表型不同。这两种情况同时发生是比较罕见的。诊断主要依靠显微镜形态和免疫表型特征。
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