Metastatic Papillary Thyroid Carcinoma Without Intrathyroidal Primary: Case Report and Literature Review.

IF 0.6 Q4 SURGERY
Case Reports in Surgery Pub Date : 2026-08-05 eCollection Date: 2026-01-01 DOI:10.1155/cris/9976142
Mohammed Sulaiman Alsayyari, Homood Mohammad Almutairi, Hassan Alshurafa, Yazeed Abdulrahman Alkhalifah, Abdulaziz Muhayya Alotaibi, Alyaa Shojaa Al Mutairy, Rawan Mosleh Alahmadi
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Abstract

Papillary thyroid carcinoma (PTC) usually has an intrathyroidal primary lesion and a good prognosis. In rare cases, however, individuals may also present with metastatic disease in the absence of a palpable thyroid primary, so-called occult PTC. Such cases are often difficult to diagnose and manage, especially when serial monitoring of serum thyroglobulin (Tg) levels and imaging studies demonstrate the opposite. We report the case of a 56-year-old woman who underwent total thyroidectomy for suspected multinodular goiter in 2019. The results of a histological examination revealed no intrathyroidal tumor in 78 blocks, but one central node was found to be positive for metastatic PTC. Follow-up examination proved that Tg had increased even though the results from U/S, PET/CT, and I-123 WB scans were always negative. Laboratory studies suggested potential heterophile antibody interference, but a fine needle aspiration (FNA) of a cervical node in 2023 and 2024 reported recurrence of metastatic PTC. She underwent left selective lateral neck dissection (levels II-V) with central compartment (level VI) exploration in January 2025, and a number of metastatic nodes without extranodal extension were found. Tg levels were undetectable throughout follow-up with no evidence of residual disease on US postoperatively. The patient remains well on long-term follow-up. We present a rare case of metastatic PTC with no identifiable thyroid primary, which is combined with the diagnostic difficulties of Tg assay interference and limitations of imaging in the follow-up setting. It highlights the importance of multimodal surveillance (including cytology, imaging, and biochemical testing) to ensure true recurrences are accurately detected, often many years after apparently curative surgery.

转移性甲状腺乳头状癌无甲状腺内原发:1例报告及文献复习。
甲状腺乳头状癌(PTC)通常有甲状腺内原发病变,预后良好。然而,在少数病例中,个体也可能在没有可触及的甲状腺原发灶的情况下出现转移性疾病,即所谓的隐匿性PTC。这些病例通常难以诊断和处理,特别是当血清甲状腺球蛋白(Tg)水平的连续监测和影像学检查显示相反的情况时。我们报告了一名56岁的女性,她在2019年因疑似多结节性甲状腺肿而接受了全甲状腺切除术。组织学检查结果显示78个肿瘤块中没有甲状腺内肿瘤,但发现一个中心淋巴结转移性PTC阳性。尽管U/S、PET/CT、I-123 WB扫描结果均为阴性,但随访证实Tg升高。实验室研究提示潜在的异性抗体干扰,但2023年和2024年宫颈淋巴结细针穿刺(FNA)报告转移性PTC复发。她于2025年1月行左侧选择性侧颈清扫术(II-V节段),并进行中央隔室(VI节段)探查,发现许多转移性淋巴结,无结外延伸。在整个随访过程中,Tg水平未检测到,术后US上没有残留疾病的证据。患者在长期随访中保持良好。我们报告一例罕见的转移性PTC,没有明确的甲状腺原发灶,这与Tg检测干扰的诊断困难和随访时影像学的局限性相结合。它强调了多模式监测(包括细胞学、影像学和生化检测)的重要性,以确保准确发现真正的复发,通常是在明显治愈的手术多年后。
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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60
审稿时长
13 weeks
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