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乳头状甲状腺癌与并存的自身免疫性甲状腺炎

Papillary Thyroid Cancer and Coexisting Autoimmune Thyroiditis.

作者信息

Veit Franziska, Graf Dieter, Momberger Saskia, Helmich-Kapp Brigitte, Ruschenburg Ilka, Peters Anja, Kussmann Jochen, Saeger Wolfgang, Schmidt Kurt Werner, Toetsch Martin, Nestler Kai, Mann Klaus

机构信息

Nuclear Medicine Center von Essen, Koblenz, Germany.

Endocrine and Nuclear Medicine Center Lüneburg, Lüneburg, Germany.

出版信息

Horm Metab Res. 2017 Nov;49(11):869-872. doi: 10.1055/s-0043-120922. Epub 2017 Nov 14.

DOI:10.1055/s-0043-120922
PMID:29136676
Abstract

Histological findings often display an association between papillary thyroid carcinomas (PTC) and autoimmune thyroiditis (AIT) and so differ significantly from follicular thyroid carcinomas (FTC). The aim of this interdisciplinary, retrospective study was to evaluate the association of AIT in patients with PTC and FTC and a control group of benign nodular goiters. One hundred thyroidectomies with histologically confirmed differentiated thyroid carcinomas, 67 with PTC and 33 with FTC, were submitted for examination. The two control groups consisted of 60 patients with euthyroid nodular goiter, displaying no signs for malignancy (no surgery) and 100 patients (second control group) with surgery of a benign nodular goiter. Controls were collected to obtain data about the incidence of significantly increased TPOAbs in the first group and of lymphocytic infiltrates (LI) in the second group. High TPOAbs were found in 35% (23/67) of patients with PTC. LI were detected by histology in 48% (32/67) of PTC. Ten patients (10/32) of this group showed the clinical and histological manifestation of a classic AIT with diffuse dense LI as well as diffuse hypoechogeneity in ultrasonography. In 7/32 cases, the histological report described focal dense LI (fAIT) and in 15/32 cases scant scattered LI. AIT and fAIT, together 25% of all PTC (17/67), showed germinal centers and can therefore be characterized as chronic autoimmune thyroiditis. In this group, high TPOAb could be detected in 94% (16/17). Scan scattered LI without germinal centers (15/32) do not represent a fAIT, although TPOAb are high in 47% (7/15). The younger age group (<45 years) showed significantly more often high TPOAbs (p<0.023) in comparison with the age-group older than 60 years. In contrast to PTC, only 4/33 (12%) patients with FTC had high TPOAb levels. We conclude that in contrast to benign euthyroid goiters and to FTC, different degrees of LI are often associated with high TPOAb levels and seem to be significantly increased in PTC, particularly prominent in younger age. There is a high coincidence between LI and high TPOAb levels. In the presence of hypoechoic thyroid nodule, signs of thyroid autoimmunity such as the presence of high TPOAbs, lymphocytic infiltration in cytology, and/or characteristic ultrasonic features, are arguments that might favor the decision for surgery if a cytologically indeterminate thyroid nodule is found and focal autonomy is excluded by szintiscan.

摘要

组织学研究结果常常显示甲状腺乳头状癌(PTC)与自身免疫性甲状腺炎(AIT)之间存在关联,因此与甲状腺滤泡癌(FTC)有显著差异。这项跨学科的回顾性研究旨在评估AIT在PTC、FTC患者以及良性结节性甲状腺肿对照组中的相关性。对100例经组织学确诊的分化型甲状腺癌患者进行了甲状腺切除术,其中67例为PTC,33例为FTC。两个对照组分别为60例甲状腺功能正常的结节性甲状腺肿患者(无恶性迹象,未进行手术)以及100例接受良性结节性甲状腺肿手术的患者(第二对照组)。收集对照组数据以获取第一组中甲状腺过氧化物酶抗体(TPOAbs)显著升高的发生率以及第二组中淋巴细胞浸润(LI)的数据。在PTC患者中,35%(23/67)检测到高TPOAbs。通过组织学检查,在67例PTC患者中有48%(32/67)检测到LI。该组中有10例患者(10/32)表现出典型AIT的临床和组织学特征,即弥漫性密集LI以及超声检查中的弥漫性低回声。在32例中的7例中,组织学报告描述为局灶性密集LI(fAIT),15例为散在稀疏LI。AIT和fAIT在所有PTC中占25%(17/67),有生发中心,因此可被归类为慢性自身免疫性甲状腺炎。在该组中,94%(16/17)可检测到高TPOAb。散在稀疏LI且无生发中心(15/32)并不代表fAIT,尽管47%(7/15)的患者TPOAb水平较高。与60岁以上年龄组相比,年龄较小的组(<45岁)中高TPOAbs的出现频率显著更高(p<0.023)。与PTC相反,FTC患者中只有4/33(12%)TPOAb水平较高。我们得出结论,与良性甲状腺功能正常的甲状腺肿和FTC不同,不同程度的LI常与高TPOAb水平相关,且在PTC中似乎显著增加,在年轻患者中尤为突出。LI与高TPOAb水平之间存在高度一致性。在存在甲状腺低回声结节的情况下,如果发现细胞学检查结果不确定的甲状腺结节且通过闪烁扫描排除了局灶性自主性,那么甲状腺自身免疫的迹象,如高TPOAbs的存在、细胞学检查中的淋巴细胞浸润和/或特征性超声特征,可能有助于支持手术决策。

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