杜胡克-伊拉克甲状腺细胞学的陷阱

F. K. Sulayvani, Asaad Shareef Omar, Sabah A. Mohammad, Azad M. Baizeed, S. Ahmed, Rose B. Hayder, Mozahim Alkhayat, Shatha D. Ahmed, I. Pity
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引用次数: 0

摘要

背景:本研究旨在确定甲状腺细针穿刺细胞学检查(FNAC)在杜霍克-伊拉克的有效性,以澄清其在当地和广泛的诊断错误。患者和方法:2013年1月至2016年12月期间,Duhok病理中心的所有甲状腺细胞学和组织学病例均被纳入本研究。将细胞学结果与相应的最终组织学结果进行比较。评估细胞学的有效性参数,并重新评估显示细胞学和组织学不符合的病例,以突出局部和文献中使用的依赖细胞学陷阱。结果:553例甲状腺活检中,良性81.6%,恶性18.4%,术前细胞学诊断及病理最终诊断仅125例。其中,除2例不满意外,只有6例(4.9%)细胞学报告被证明与相应的组织学结果不匹配。其余117例(95.1%)病例显示两种评价试验完全一致。细胞学预测恶性肿瘤的比例为82.9%,敏感性为94.3%,特异性为95.5%。6例不匹配病例均在无图像引导下盲目吸痰,4例假阳性,假阳性率3.2%,阳性预测值89.2%。其余2例为假阴性细胞学,假阴性率为1.6%,阴性预测值为97.7%。细胞学上,5例(83.3%)不匹配涂片,4例假阳性,1例假阴性,出现在富含淋巴细胞的甲状腺病变的涂片中,尤其是桥本氏病。假阳性的陷阱包括2个误诊为乳头状癌的高细胞涂片,1个误诊为滤泡癌的核异型大细胞,1个误诊为淋巴瘤的淋巴样增生。另一方面,低细胞涂片上不明确的非典型淋巴样细胞未被诊断为低级别MALT淋巴瘤,细胞学标准不明确则错过了乳头状癌的诊断。结论:富含淋巴细胞的甲状腺涂片应由经验丰富的细胞病理学家结合临床、放射学和细胞学检查结果进行解释,因为此类病例可能会出现某些细胞形态学缺陷,从而降低细胞学检查的有效性。在可疑的情况下,应该进行进一步的测试,以克服单独应用时功能的限制和缺陷。杜霍克医学杂志2019;13(1): 83-95。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
PITFALLS OF THYROID CYTOLOGY IN DUHOK-IRAQ
Background: The current study was undertaken to determine the validity of thyroid fine needle aspiration cytology (FNAC) in Duhok-Iraq to clarify its traded diagnostic errors locally and broadly. Patients and Methods: All thyroid cytologic and histologic cases referred to Duhok Pathology Centers, between January 2013 and December 2016, were enrolled in this study. Cytologic findings were compared with their corresponding final histologic results. The validity parameters of cytology were assessed and cases showing cytologic and histologic non-conformance were re-evaluated to highlight the dependant cytologic pitfalls used locally and in the literature. Results: Of 553 thyroid biopsies with 81.6% benign and 18.4% malignant, only 125 cases had preoperative diagnostic cytology and subsequent histologic final diagnoses. Of these, apart from 2 unsatisfactory cases, only 6 (4.9%) cytologic reports were proved not to be matched with their corresponding histologic results. The remaining 117 (95.1%) cases showed complete agreement between the two evaluation tests. Malignancy was predicted by cytology in 82.9%with a sensitivity of 94.3% and specificity of 95.5%. All the 6 unmatched cases were aspirated blindly with no image guide, 4 were false positive resulting in 3.2%false positive rate and 89.2% positive predictive value. The remaining unmatched 2 cases were false negative cytologies that gave 1.6% false negative rate and 97.7% negative predictive value. Cytologically, 5 (83.3%) unmatched smears, 4 false positive and 1 false negative, appeared in smears of lymphocyte-rich thyroid lesions, particularly Hashimoto’s. The false positive pitfalls comprised 2 over diagnosis of hypercellular smears showing some features of papillary carcinoma, 1 overestimation of the large cells with nuclear atypia as follicular carcinoma and 1 over diagnosis of lymphoid hyperplasia as lymphoma. On the other hand, low cellular smears with unclear atypical lymphoid cells underdiagnosed low grade MALT lymphoma and unobvious cytologic criteria missed the diagnosis of papillary carcinoma. Conclusions: Lymphocyte-rich thyroid smears should be interpreted by experienced cytopathologists in the context of clinical, radiological and cytologic findings as suchcases may give certain cytomorphologic pitfalls that may decrease the cytologic validity. In suspicious cases, further tests should be justified to overcome the limitations and pitfalls of features when applied alone. Duhok Med J 2019; 13 (1): 83-95.
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