A 46-Year-Old Man with an Incidental Finding of a Papillary Thyroid Carcinoma in a Thyroglossal Duct Cyst.

IF 1 Q3 MEDICINE, GENERAL & INTERNAL American Journal of Case Reports Pub Date : 2024-12-31 DOI:10.12659/AJCR.945625
Agnieszka Witkowska, Piotr Aleksander Rot, Andrzej Franciszek Wojdas
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Abstract

BACKGROUND The thyroglossal duct cyst, which develops from the midline migratory tract between the foramen cecum and the anatomic location of the thyroid, is the most prevalent congenital abnormality of the neck, accounting for about 70% of all cervical neck masses in children and 7% in adults. Only up to 1% of these abnormalities contain malignant thyroid tissue, with 90% of those cases being papillary thyroid carcinoma. Thyroglossal duct cyst is rarely linked to carcinoma. Clinical presentation of thyroglossal duct cyst carcinoma is generally impossible to differentiate from benign tumors before surgery, and most cases are incidentally detected after surgery, due to histopathological evaluation of the resected cyst. CASE REPORT A 46-year-old man presented with a painless, progressively enlarging neck lump. Physical examination identified a well-defined, mildly firm mass situated anteroinferior to the hyoid bone. Imaging indicated that a thyroid gland duct cyst was the most likely diagnosis. The patient underwent the Sistrunk procedure. Histopathological analysis revealed papillary thyroid carcinoma within the thyroid gland duct cyst. CONCLUSIONS Carcinomas occurring in the thyroglossal cyst are uncommon. The causes of thyroglossal duct carcinoma are unclear, and neither a detailed medical history nor a physical examination can reliably diagnose it before surgery. The management of such cases remains debated, owing to the rarity of reported occurrences. So far, the standard treatment involves the Sistrunk procedure, followed by close patient monitoring. For patients with metastatic disease, a total thyroidectomy is necessary, and if neck metastases are present, neck dissection is required.

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一个46岁的男性偶然发现甲状腺乳头状癌在甲状腺舌管囊肿。
背景:甲状腺舌管囊肿起源于盲肠孔与甲状腺解剖位置之间的中线迁移道,是最常见的颈部先天性异常,约占儿童颈椎肿块的70%,成人约占7%。这些异常中只有1%含有恶性甲状腺组织,其中90%为甲状腺乳头状癌。甲状舌管囊肿很少与癌有关。甲状腺舌管囊肿癌的临床表现术前一般无法与良性肿瘤区分,多数病例是术后偶然发现的,这是由于对切除囊肿的组织病理学评估。病例报告一名46岁男性,颈部肿块无痛,逐渐增大。体格检查发现在舌骨前下方有一个轮廓清晰、轻度坚硬的肿块。影像显示甲状腺导管囊肿是最有可能的诊断。病人接受了西斯特伦克手术。组织病理学分析显示为甲状腺导管囊肿内的甲状腺乳头状癌。结论甲状舌囊肿中发生的癌并不常见。甲状腺舌管癌的病因尚不清楚,术前详细的病史和体格检查都不能可靠地诊断。由于报告的病例很少,对这类病例的处理仍有争议。到目前为止,标准治疗包括Sistrunk程序,然后是密切监测患者。对于转移性疾病的患者,甲状腺全切除术是必要的,如果存在颈部转移,则需要进行颈部清扫。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
American Journal of Case Reports
American Journal of Case Reports Medicine-Medicine (all)
CiteScore
1.80
自引率
0.00%
发文量
599
期刊介绍: American Journal of Case Reports is an international, peer-reviewed scientific journal that publishes single and series case reports in all medical fields. American Journal of Case Reports is issued on a continuous basis as a primary electronic journal. Print copies of a single article or a set of articles can be ordered on demand.
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