涎腺活检病灶评分≥1的干燥综合征患者的临床、组织病理学和免疫组织化学特征

Andrés Felipe Lamos-Duarte, Rafael Parra-Medina, Carlos Santiago Rivadeneira-Chamorro, Juan Pablo Castañeda-González, Alejandro Escobar, Adriana Rojas-Villarraga, Gabriel Santiago Rodríguez-Vargas, Ana María Arredondo, Héctor Cubides, José Fernando Polo, Juan José Capasso, Claudia Ibañez, Jairo Hernán Cajamarca-Barón
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引用次数: 0

摘要

简介:Sjögren综合征是一种全身性自身免疫性疾病。免疫组织化学在小唾液腺活检中的有用性已被描述为有助于在难以诊断的病例中间接表征淋巴细胞表型。目的:描述sicca综合征患者的社会人口学、临床、血清学、组织病理学和免疫组织化学变量,且轻微唾液腺活检病灶评分大于或等于1。材料和方法:我们进行了一项观察性、回顾性研究,纳入了正在研究的潜在干燥综合征患者,这些患者进行了小涎腺活检,并且焦点评分大于或等于1。小唾液腺活检行免疫组化,CD8 T淋巴细胞染色红,CD4 T淋巴细胞染色棕。使用MoticEasyScan Pro 6™(MOTIC)设备和QuPath™软件检测CD20:CD3和CD4:CD8标记物的表达比。定性变量分析采用卡方检验或Fisher精确检验,定量变量分析采用正态假设。结果:分析28例患者,其中Sjögren综合征16例,多自身免疫8例。发现小唾液腺活检萎缩与多自身免疫的发展之间存在关联(OR = 11.1;95% ci: 1.12-112;P值= 0.033)。CD20:CD3和CD4:CD8比值正常,Sjögren综合征患者与非Sjögren综合征患者无统计学差异。在Sjögren综合征患者亚组中,CD4 T淋巴细胞占主导地位,16例患者中有15例CD4:CD8比值等于或大于2:1。结论:Sjögren综合征患者的腺体萎缩与多自身免疫的发展和CD4 T淋巴细胞的优势有关。这一发现突出了本组小涎腺活检免疫组织化学的潜在价值。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Clinical, histopathological, and immunohistochemical characteristics of patients with sicca syndrome with a focus score ≥ 1 in the minor salivary gland biopsy

Introduction: Sjögren’s syndrome is a systemic autoimmune disease. The usefulness of immunohistochemistry in minor salivary gland biopsies has been described to be helpful in indirectly characterizing the lymphocyte phenotype in difficult diagnosis cases.

Objective: To describe sociodemographic, clinical, serological, histopathological, and immunohistochemical variables in patients with sicca syndrome and a minor salivary gland biopsy focus score greater than or equal to one.

Materials and methods: We conducted an observational, retrospective study that included patients under study for potential sicca syndrome whose minor salivary gland biopsy was available and had obtained a focus score greater than or equal to one. Immunohistochemistry was performed on the minor salivary gland biopsy with chromogen red staining for CD8 T lymphocytes and brown staining for CD4 T lymphocytes. Expression ratio of CD20:CD3 and CD4:CD8 markers was determined with the MoticEasyScan Pro 6™ (MOTIC) device and the QuPath™ software. Qualitative variables were analyzed using the chi-square or Fisher’s exact test, and quantitative variables were analyzed according to their assumption of normality.

Results: Twenty-eight patients were analyzed: 16 patients had Sjögren’s syndrome, and 8 of them had polyautoimmunity. An association was found between atrophy in the minor salivary gland biopsy and development of polyautoimmunity (OR = 11.1; 95% CI: 1.12-112; p value = 0.033). The CD20:CD3 and CD4:CD8 ratios were normal, with no statistically significant differences between patients with and without Sjögren’s syndrome. In the subgroup of patients with Sjögren’s syndrome, CD4 T lymphocytes were predominant, with 15 cases out of 16 with CD4:CD8 ratios equal to or greater than 2:1.

Conclusions: Glandular atrophy was associated with the development of polyautoimmunity and a predominance of CD4 T lymphocytes in patients with Sjögren’s syndrome. This finding highlights the potential value of immunohistochemistry of minor salivary gland biopsies in this group.

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