Sahin Davut, Akpolat İlkser
Department of Pathology, Acibadem Health Group, Istanbul, Turkey.
Department of Pathology, Acibadem University, Medical Faculty, Istanbul, Turkey.
Diagn Cytopathol. 2019 Dec;47(12):1251-1258. doi: 10.1002/dc.24294. Epub 2019 Jul 31.
The aims of the study are to identify the diagnostic cytological features of subacute granulomatous thyroiditis (SGT), to compare our results with previous literature studies, and to investigate the cytological changes in SGT that mimic other thyroid lesions.
This retrospective study was conducted with 69 cases. The cytology slides were re-evaluated. The diagnostic cytomorphological features of the disease were identified. The results were compared with the literature. Differential diagnosis of the disease is discussed with the results obtained.
The diagnostic cytological features consisted of lymphocytes, multinucleated giant cells, loose epithelioid histiocyte groups, granulomas, isolated epithelioid histiocytes, colloid, and neutrophil leukocytes. The highest degree of concordance between our results and the published literature was the presence of giant cells while the lowest was for microfollicles. Some reactive cytological features of SGT were similar to other benign or malignant diseases of the thyroid.
SGT is a rare and self-limiting disease. Cytological features are not specific. The diagnosis should be confirmed by clinical and laboratory results. Reactive atypia in the early phase of the disease and microfollicles in the late phase may lead to a false cytological diagnosis, thus resulting in unnecessary resection. To prevent such misdiagnoses, cytopathologists should be aware of the reactive cytological changes in this disorder.
本研究的目的是确定亚急性肉芽肿性甲状腺炎(SGT)的诊断性细胞学特征,将我们的结果与先前的文献研究进行比较,并研究SGT中模仿其他甲状腺病变的细胞学变化。
本回顾性研究纳入69例病例。对细胞学玻片进行重新评估。确定该疾病的诊断性细胞形态学特征。将结果与文献进行比较。根据所得结果讨论该疾病的鉴别诊断。
诊断性细胞学特征包括淋巴细胞、多核巨细胞、松散的上皮样组织细胞群、肉芽肿、孤立的上皮样组织细胞、胶质和中性粒细胞。我们的结果与已发表文献之间一致性最高的是巨细胞的存在,而最低的是微滤泡。SGT的一些反应性细胞学特征与甲状腺的其他良性或恶性疾病相似。
SGT是一种罕见的自限性疾病。细胞学特征不具有特异性。诊断应通过临床和实验室结果来证实。疾病早期的反应性异型性和晚期的微滤泡可能导致错误的细胞学诊断,从而导致不必要的切除。为防止此类误诊,细胞病理学家应了解这种疾病中的反应性细胞学变化。