Kim Eunji, Park Jun Hyun, Park Ji-Young, Lee Sang-Woo, Jung Jin Hyang
Division of Thyroid and Endocrine Surgery, Department of Surgery, Kyungpook National University Chilgok Hospital, Daegu, Korea.
Department of Pathology, Kyungpook National University Chilgok Hospital, School of Medicine, Kyungpook National University, Daegu, Korea.
Ann Surg Treat Res. 2025 Aug;109(2):105-112. doi: 10.4174/astr.2025.109.2.105. Epub 2025 Jul 30.
Oncocytic carcinoma (OCA) has been reclassified from follicular thyroid carcinoma due to its unique features. Its rarity has resulted in limited studies on differentiating OCA from oncocytic adenoma (OA). This study aimed to compare the clinicopathologic and preoperative features of OCA and OA and evaluate the effectiveness of ultrasonography and cytology.
We conducted a retrospective study involving 83 patients (23 with OCA and 60 with OA) who underwent thyroid surgery between 2011 and 2024. We reviewed clinical, ultrasonographic, cytologic, and histopathologic data to assess diagnostic performance.
OCA cases had larger tumors than OA in both sonographic (4.2 ± 1.7 cm 2.7 ± 1.4 cm, P < 0.001) and pathologic measurements (3.8 ± 1.7 cm 2.3 ± 1.4 cm, P < 0.001). K-TIRADS (the Korean Thyroid Imaging Reporting and Data System) did not effectively distinguish OCA from OA; however, ACR TI-RADS (the American College of Radiology Thyroid Imaging Reporting and Data System) categorized more OCA cases into higher-risk groups (17.4% 1.7%, P = 0.016). Trabecular formation and intranodular vascularity were more frequent in OCA (17.4% 1.7%, P = 0.019; 65.2% 33.3%, P = 0.049). Cytologically, 87% of OCAs were classified as follicular neoplasms compared to 20% of OAs.
Predicting malignancy in oncocytic neoplasms is challenging. Larger tumor size, higher ACR TI-RADS scores, and trabecular formation are potential indicators for OCA. Cytologic subcategorization within Bethesda IV suggests follicular neoplasms carry a higher malignancy risk than oncocytic neoplasms. Multicenter studies are needed to validate these findings.
嗜酸细胞癌(OCA)因其独特特征已从滤泡状甲状腺癌中重新分类。其罕见性导致关于区分OCA与嗜酸细胞腺瘤(OA)的研究有限。本研究旨在比较OCA和OA的临床病理及术前特征,并评估超声检查和细胞学检查的有效性。
我们进行了一项回顾性研究,纳入了2011年至2024年间接受甲状腺手术的83例患者(23例OCA和60例OA)。我们回顾了临床、超声、细胞学和组织病理学数据以评估诊断性能。
在超声测量(4.2±1.7 cm对2.7±1.4 cm,P<0.001)和病理测量(3.8±1.7 cm对2.3±1.4 cm,P<0.001)中,OCA病例的肿瘤均比OA大。韩国甲状腺影像报告和数据系统(K-TIRADS)不能有效区分OCA和OA;然而,美国放射学会甲状腺影像报告和数据系统(ACR TI-RADS)将更多OCA病例归类为高风险组(17.4%对1.7%,P = 0.016)。小梁形成和结节内血管在OCA中更常见(17.4%对1.7%,P = 0.019;65.2%对33.3%,P = 0.049)。细胞学上,87%的OCA被分类为滤泡性肿瘤,而OA为20%。
预测嗜酸细胞性肿瘤的恶性程度具有挑战性。更大的肿瘤大小、更高的ACR TI-RADS评分和小梁形成是OCA的潜在指标。贝塞斯达IV类中的细胞学亚分类表明滤泡性肿瘤比嗜酸细胞性肿瘤具有更高的恶性风险。需要多中心研究来验证这些发现。