Medical Center Hormony, Vinnytsia, Ukraine.
Laboratory of Pathology "CSD Health Care", Kyiv, Ukraine.
J Med Case Rep. 2024 Jan 15;18(1):17. doi: 10.1186/s13256-023-04313-1.
We present a rare case of thyroid lesion marked as the Warthin-like variant of papillary thyroid carcinoma (WLV-PTC) with lymph node metastases. A proper preoperative identification is difficult because of unspecific cytology features and common ultrasound characteristics of this malignant tumor. The long-term prognosis cannot be thoroughly described due to the scarcity of data. The purpose of the presentation is to show common characteristics and long-term survival rates of an uncommon variant of differentiated thyroid cancer (DTC). Therefore, the data represented in this article can make a significant contribution to future investigations.
A 40-year-old Ukrainian woman had a lesion in the thyroid gland, which was accidentally diagnosed during medical checkup. Ultrasound (US) features were similar to the common suspicious nodule. It had typical signs of suspicion for malignancy (TI-RADS-4) on the background of thyroiditis. A thorough investigation of the neck showed lymph nodes with nonspecific US features on both lateral compartments. Lymph nodes were hypoechoic, oval-shaped and 10 mm wide, with regular contours, low central vascularity, with preserving hilar fat, without cystic formation. The patient did not have any complaints or changes in the hormone status. No hereditary findings linked with cancer were discovered. The woman had been living for a long time in the country with a high level of insolation, which was atypical for the ordinary environment of the patient. Fine-needle aspiration (FNA) of the lesion was done and the Bethesda system 6 result was obtained. Total thyroidectomy with central lymph node dissection was accomplished. The histological conclusion was WLV-PTC on the background of lymphocytic infiltration of the gland with metastasis to the lymph nodes. The inpatient radioactive iodine (RAI) ablation (100 mCi) was subsequently performed. Hormone withdrawal was used followed by RAI. In one year after the surgery the level of thyroglobulin (Tg) was 0.2 ng/ml. Up to the present time the five-year follow-up has not demonstrated any signs of recurrence relying on a level of Tg (< 0.04 ng/ml), Tg antibodies (< 14 IU/ml), neck US without any structural disease.
WLV-PTC resembles salivary gland tumors with similar histological features. This variant is not well known, but often associated with a stroma lymphocytic infiltration and a low risk of lymph node metastases. It is regarded that this rare subtype has similar long-term survival rates as classic papillary thyroid cancer (PTC).
我们报告了一例罕见的甲状腺病变,其标记为具有淋巴结转移的沃辛样甲状腺乳头状癌(WLV-PTC)。由于这种恶性肿瘤的细胞学特征不特异和常见的超声特征,术前正确识别很困难。由于数据稀缺,长期预后无法彻底描述。本文的目的是展示分化型甲状腺癌(DTC)的罕见变异型的常见特征和长期生存率。因此,本文所代表的数据对未来的研究具有重要意义。
一位 40 岁的乌克兰女性在体检中意外发现甲状腺有一处病变。超声(US)特征类似于常见可疑结节。在甲状腺炎的背景下,具有典型的恶性可疑征象(TI-RADS-4)。对颈部的彻底检查显示,双侧颈外侧区的淋巴结具有非特异性的 US 特征。淋巴结呈低回声,椭圆形,宽 10mm,轮廓规则,中央血管化程度低,保留 hilar 脂肪,无囊性形成。患者没有任何不适或激素状态的变化。未发现与癌症相关的遗传性发现。该女性长期居住在一个高光照水平的国家,这与患者的普通环境不符。对病变进行了细针抽吸(FNA),并获得了 Bethesda 系统 6 的结果。完成了全甲状腺切除术和中央淋巴结清扫术。组织学结论是淋巴细胞浸润的甲状腺背景下的 WLV-PTC,并伴有淋巴结转移。随后进行了住院放射性碘(RAI)消融(100mCi)。随后进行了激素撤退和 RAI。手术后一年,甲状腺球蛋白(Tg)水平为 0.2ng/ml。截至目前,五年随访未发现任何复发迹象,依赖于 Tg(<0.04ng/ml)、Tg 抗体(<14IU/ml)、无结构疾病的颈部 US。
WLV-PTC 与具有相似组织学特征的唾液腺肿瘤相似。这种变异型不太为人所知,但常与间质淋巴细胞浸润和低淋巴结转移风险相关。人们认为这种罕见的亚型与经典的甲状腺乳头状癌(PTC)具有相似的长期生存率。