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自身免疫性甲状腺炎细胞学诊断中的陷阱。

Pitfalls in cytological diagnosis of autoimmune thyroiditis.

作者信息

Kumarasinghe M P, De Silva S

机构信息

Department of Pathology, Faculty of Medicine, University of Colombo, Sri Lanka.

出版信息

Pathology. 1999 Feb;31(1):1-7. doi: 10.1080/003130299105430.

Abstract

The aims of this study are to document pitfalls in cytologic diagnosis of autoimmune thyroiditis (AT) and highlight possible ways to minimize them. One hundred consecutive thyroid aspirates with features diagnostic or suggestive of AT, performed and reported by the first author, were included in the study. Follow-up was traced and cytologic features responsible for indecisiveness were re-assessed in those reported as suggestive of AT. The features were then correlated with the results of serologic and thyroid function tests and clinical features, and an attempt was made to amend the final diagnosis using an integrated approach. Seventy eight were diagnostic and 22 were suggestive of AT. In the latter 22, features responsible for the indecisiveness were: cytologic atypia, in the form of nuclear enlargement, irregularity and grooves and altered chromatin texture, in 14 (64%); nucleoli with suspicion of a coexisting neoplasm in three (13.6%), two of which showed epithelial preponderance, crowding and discohesion; sparse inflammation in four (18%); a predominant lymphoid population without epithelial cells resembling a reactive lymph node in one (4.5%); co-existing toxic features in two (9%); and scanty smears in one (4.5%). Eighteen of the 22 suspected of AT had follow-up. Six had been assessed histologically; three with features suspicious of a neoplasm were diagnosed respectively as a papillary carcinoma (PC), Hurthle cell carcinoma (HCC) and a multinodular goitre (MNG) with degenerate changes. The other three were confirmed as AT; one with cytologic atypia, one with sparse inflammation and the third as cytologically resembling a reactive lymphnode. In ten of the remaining 12, the final diagnosis could be revised following an integrated approach with possible reduction of the indecisiveness. Potential pitfalls are: cytologic atypia occurring in AT; abundance or scarcity of background inflammation; low cell yield; and co-existing toxicity and malignancies. Epithelial preponderance over inflammation, nuclear crowding, severe atypia and cell discohesion should raise the possibility of a neoplasm in spite of other features of AT. Awareness of possible pitfalls and adopting an integrated approach, especially in difficult situations, will minimize pitfalls.

摘要

本研究的目的是记录自身免疫性甲状腺炎(AT)细胞学诊断中的陷阱,并强调将这些陷阱降至最低的可能方法。本研究纳入了由第一作者进行并报告的100例具有AT诊断特征或疑似AT特征的连续甲状腺穿刺样本。进行随访,并对那些报告为疑似AT的样本中导致诊断不明确的细胞学特征进行重新评估。然后将这些特征与血清学、甲状腺功能检查结果及临床特征进行关联,并尝试采用综合方法修正最终诊断。其中78例为诊断性病例,22例为疑似AT病例。在这22例疑似病例中,导致诊断不明确的特征有:14例(64%)表现为细胞核增大、形态不规则、有核沟及染色质结构改变等细胞学异型性;3例(13.6%)可见核仁,怀疑合并肿瘤,其中2例表现为上皮细胞增多、拥挤及细胞间黏附丧失;4例(18%)炎症细胞稀少;1例(4.5%)以淋巴细胞为主,无上皮细胞,类似反应性淋巴结;2例(9%)合并毒性特征;1例(4.5%)涂片细胞量少。22例疑似AT病例中有18例进行了随访。6例进行了组织学评估;3例具有肿瘤可疑特征的病例分别被诊断为乳头状癌(PC)、嗜酸性细胞癌(HCC)和具有退行性改变的多结节性甲状腺肿(MNG)。另外3例确诊为AT;1例有细胞学异型性,1例炎症细胞稀少,第3例细胞学表现类似反应性淋巴结。在其余12例中的10例中,采用综合方法可修正最终诊断,可能减少诊断的不明确性。潜在的陷阱包括:AT中出现的细胞学异型性;背景炎症的丰富或稀少;细胞产量低;以及合并毒性和恶性肿瘤。尽管有AT的其他特征,但上皮细胞多于炎症细胞、细胞核拥挤、严重异型性及细胞间黏附丧失应增加肿瘤的可能性。认识到可能的陷阱并采用综合方法,尤其是在困难情况下,将使陷阱降至最低。

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