甲状舌管囊肿癌:病例报告

Carolina Meller Jost, Claudiane Machado Visintin, Robledo Meller Alievi
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摘要

简介甲状舌管囊肿(TDC)被认为是甲状腺发育过程中最常见的先天性异常,估计发病率占总人口的7%。虽然这些囊肿绝大多数是良性的,但约有1%的病例可能会恶变。目的:报告一名甲状舌管囊肿发展为癌的患者的病史、演变和治疗情况,回顾该疾病的病理生理学和相关的稀缺文献。病例摘要:40 岁女性,2018 年诊断为 TDC。她于 2020 年到头颈外科医生处复查,向医生报告结节增大,局部不适。医生建议进行手术切除。手术后进行的解剖病理学检查显示,怀疑存在恶性转化。进行了免疫组化检查,证实了这一怀疑。患者被要求在 6 个月后复诊,并接受超声波检查以监测病理情况。讨论:甲状舌管导致甲状腺从舌根部下降,最终停留在颈部中线的前方区域。该管道应在胎儿期开始时闭塞;如果闭塞失败,就会在该管道中形成囊肿。这种囊肿通常在上呼吸道感染后才会被发现,在极少数情况下,囊肿壁会发生癌变。结论CDT 癌症病例在文献中的报道很少,而且在临床上的发病率也很低,因此应该对这些病例进行讨论。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Thyroglossal duct cyst carcinoma: Case report
Introduction: Considered the most common congenital anomaly in the development of the thyroid gland, the thyroglossal duct cyst (TDC) has an estimated prevalence of 7% of the population. Although the vast majority of these cysts are benign, around 1% of cases can become malignant. Aim: To report the history, evolution and management of a patient with a thyroglossal duct cyst that developed into a carcinoma, to review the pathophysiology of the disease and the scarce literature on the subject. Case summary: 40-year-old woman diagnosed in 2018 with TDC. She went to a head and neck surgeon in 2020 for a reassessment of the case, to whom she reported an increase in the nodule and local discomfort. Surgery was indicated to remove it. The anatomopathological examination carried out after the surgery revealed a suspicion of malignant transformation. An immunohistochemical test was carried out, which confirmed the suspicion. The patient was asked to return in 6 months and to undergo ultrasound to monitor the pathology. Discussion: The thyroglossal duct results in the thyroid descending from the base of the tongue to its final resting place in the anterior region of the neck in the midline. This tract should obliterate at the beginning of fetal life; failure in this involution can subsequently give rise to a cyst in this duct. The cyst is often noticed after an upper respiratory tract infection and, in rare cases, a carcinoma can develop from the walls of the cyst. Conclusion: CDT carcinoma cases should be discussed due to the scarcity of reports in the literature and their rare incidence in the clinical field.
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