Unusual case of medullary thyroid cancer

Michał Leszczyński, Daniel Majszyk
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Abstract

Medullary thyroid carcinomas make up 9,4% of all cancers of the thyroid gland [1]. We can divide them into sporadic and familial form. Sporadic forms are most common. The rest of medullary thyroid carcinomas are familial forms which in most cases are associated with MEN2a and MEN2b syndromes. If neoplasm is associated with MEN2a or MEN2b syndromes, other tumors can occur: pheochromocytoma or adenomas of parathyroids glands. Medullary thyroid carcinoma typically occurs as a solid tumor in the thyroid region of the neck. It can produce also: pain in thyroid region, dysphagia, hoarseness, cervical lymphadenopathy. These symptoms are caused by infiltration of adjacent tissues by neoplasm and by metastases to cervical lymph nodes. It is very rare that there is no tumor in the thyroid region, when a patient complains about signs associated with infiltration of the tumor, but in some cases lymphadenopathy can be the first sign of medullary thyroid carcinoma [2]. Rarer than that there is no tumor in thyroid gland visualized in CT scans when there are signs of cervical lymphadenopathy. In this case report we present the patient with metastases of the medullary thyroid carcinoma to the neck and no other findings in physical examination and additional testing.
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甲状腺髓样癌的罕见病例
甲状腺髓样癌占所有甲状腺癌的9.4%。我们可以把它们分为散发性和家族性。零星的形式是最常见的。其余的甲状腺髓样癌为家族型,在大多数情况下与MEN2a和MEN2b综合征有关。如果肿瘤与MEN2a或MEN2b综合征相关,则可发生其他肿瘤:嗜铬细胞瘤或甲状旁腺腺瘤。甲状腺髓样癌通常发生在颈部甲状腺区域的实体瘤。还可引起甲状腺疼痛、吞咽困难、声音嘶哑、颈淋巴肿大。这些症状是由肿瘤浸润邻近组织和转移到颈部淋巴结引起的。当患者抱怨肿瘤浸润的征象时,甲状腺区域没有肿瘤是非常罕见的,但在某些情况下,淋巴结病变可能是甲状腺髓样癌的第一个征象。更罕见的是,当有颈部淋巴结病变的征象时,CT扫描显示甲状腺无肿瘤。在这个病例报告中,我们提出了甲状腺髓样癌转移到颈部的患者,在体格检查和其他检查中没有其他发现。
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来源期刊
Polish Otorhinolaryngology Review
Polish Otorhinolaryngology Review Medicine-Otorhinolaryngology
CiteScore
0.20
自引率
0.00%
发文量
23
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