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钙化性纤维性肿瘤:是否为IgG4相关性疾病?

Calcifying fibrous tumour: An IgG4-related disease or not?

作者信息

Hu Yu-Hsuan, Yu Chen-Tang, Chen Chih-Jung, Wen Mei-Chin

机构信息

Department of Pathology and Laboratory Medicine, Taichung Veterans General Hospital, Taichung, Taiwan.

Department of Pediatrics, Changhua Christian Hospital, Changhua, Taiwan.

出版信息

Int J Exp Pathol. 2020 Feb;101(1-2):38-44. doi: 10.1111/iep.12339. Epub 2020 Feb 23.

Abstract

Calcifying fibrous tumour (CFT) has some of the histopathological features, such as abundant plasma cells and stromal fibrosis, that are exhibited by IgG4-related diseases (IgG4-RD). The possible role of IgG4-positive plasma cells in calcifying fibrous tumour was investigated. The aim of this study was to determine any potential relationship between IgG4-RD and CFT. Thirteen cases with a total of 16 CFTs were reviewed. Lesion samples were immunostained with anti-IgG4 and anti-IgG antibodies. The number of IgG4-positive and IgG-positive plasma cells (IgG + PC) and their ratios were estimated. Plasma cells were found in all tumours. IgG4-positive plasma cells ranged from 0 to 71 per high-power field (HPF; mean 17.8/HPF), and IgG + PC ranged from 2 to 93/HPF (mean 42.6/HPF). The IgG4/IgG ratio ranged from 0% to 80% (mean 29%). There were seven tumours with the ratio of IgG4/IgG + PC that exceeded 40%. Various degrees of stromal fibrosis were present in eight tumours. All tumours have variable calcification. The histopathological features of CFT were found to be similar to those of IgG4-RD. Some CFT also showed a high number of IgG4-positive plasma cells, and the ratio of IgG4/IgG + PC exceeded 40%, most notably in patients with concomitant inflammatory or autoimmune disease. The long-term follow-up showed no evidence of IgG4-RD in any of these patients. Our findings suggest that while CFT overlaps morphologically with IgG4-RD, it probably should not be classified as an IgG4-RD.

摘要

钙化性纤维瘤(CFT)具有一些组织病理学特征,如丰富的浆细胞和间质纤维化,这些特征也见于IgG4相关疾病(IgG4-RD)。本研究调查了IgG4阳性浆细胞在钙化性纤维瘤中的可能作用。本研究的目的是确定IgG4-RD与CFT之间是否存在潜在关系。回顾了13例共16个CFT病例。病变样本用抗IgG4和抗IgG抗体进行免疫染色。估计IgG4阳性和IgG阳性浆细胞(IgG + PC)的数量及其比例。所有肿瘤中均发现有浆细胞。IgG4阳性浆细胞每高倍视野(HPF)为0至71个(平均17.8/HPF),IgG + PC每HPF为2至93个(平均42.6/HPF)。IgG4/IgG比例为0%至80%(平均29%)。有7个肿瘤的IgG4/IgG + PC比例超过40%。8个肿瘤存在不同程度的间质纤维化。所有肿瘤均有不同程度的钙化。发现CFT的组织病理学特征与IgG4-RD相似。一些CFT也显示出大量IgG4阳性浆细胞,且IgG4/IgG + PC比例超过40%,在伴有炎症或自身免疫性疾病的患者中尤为明显。长期随访显示这些患者中均无IgG4-RD的证据。我们的研究结果表明,虽然CFT在形态学上与IgG4-RD有重叠,但它可能不应被归类为IgG4-RD。

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