首页> 外文期刊>Annals of the Rheumatic Diseases: A Journal of Clinical Rheumatology and Connective Tissue Research >Proposal for a new clinical entity, IgG4-positive multiorgan lymphoproliferative syndrome: analysis of 64 cases of IgG4-related disorders.
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Proposal for a new clinical entity, IgG4-positive multiorgan lymphoproliferative syndrome: analysis of 64 cases of IgG4-related disorders.

机译:关于新的临床实体IgG4阳性多器官淋巴组织增生综合征的建议:分析64例IgG4相关疾病。

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BACKGROUND: Mikulicz's disease (MD) has been considered as one manifestation of Sjogren's syndrome (SS). Recently, it has also been considered as an IgG(4)-related disorder. OBJECTIVE: To determine the differences between IgG(4)-related disorders including MD and SS. METHODS: A study was undertaken to investigate patients with MD and IgG(4)-related disorders registered in Japan and to set up provisional criteria for the new clinical entity IgG(4)-positive multiorgan lymphoproliferative syndrome (IgG(4)+MOLPS). The preliminary diagnostic criteria include raised serum levels of IgG(4) (>135 mg/dl) and infiltration of IgG(4)(+) plasma cells in the tissue (IgG(4)+/IgG+ plasma cells >50%) with fibrosis or sclerosis. The clinical features, laboratory data and pathologies of 64 patients with IgG(4)+MOLPS and 31 patients with typical SS were compared. RESULTS: The incidence of xerostomia, xerophthalmia and arthralgia, rheumatoid factor and antinuclear, antiSS-A/Ro and antiSS-B/La antibodies was significantly lower in patients with IgG(4)+MOLPS than in those with typical SS. Allergic rhinitis and autoimmune pancreatitis were significantly more frequent and total IgG, IgG(2), IgG(4) and IgE levels were significantly increased in IgG(4)+MOLPS. Histological specimens from patients with IgG(4)+MOLPS revealed marked IgG(4)+ plasma cell infiltration. Many patients with IgG(4)+MOLPS had lymphocytic follicle formation, but lymphoepithelial lesions were rare. Few IgG(4)+ cells were seen in the tissue of patients with typical SS. Thirty-eight patients with IgG(4)+MOLPS treated with glucocorticoids showed marked clinical improvement. CONCLUSION: Despite similarities in the involved organs, there are considerable clinical and pathological differences between IgG(4)+MOLPS and SS. Based on the clinical features and good response to glucocorticoids, we propose a new clinical entity: IgG(4)+MOLPS.
机译:背景:Mikulicz病(MD)被认为是干燥综合征(SS)的一种表现。最近,它也被认为是与IgG(4)相关的疾病。目的:确定包括MD和SS在内的IgG(4)相关疾病之间的差异。方法:进行了一项研究,以调查在日本注册的患有MD和IgG(4)相关疾病的患者,并为新的临床实体IgG(4)阳性多器官淋巴组织增生综合征(IgG(4)+ MOLPS)建立临时标准。初步诊断标准包括升高的血清IgG(4)(> 135 mg / dl)和组织中IgG(4)(+)浆细胞的浸润(IgG(4)+ / IgG +浆细胞> 50%)纤维化或硬化。比较了64例IgG(4)+ MOLPS患者和31例典型SS患者的临床特征,实验室数据和病理。结果:IgG(4)+ MOLPS患者的口干,口干和关节痛,类风湿因子和抗核,抗SS-A / Ro和抗SS-B / La抗体的发生率明显低于典型SS患者。变应性鼻炎和自身免疫性胰腺炎的发生率明显更高,并且IgG(4)+ MOLPS中的总IgG,IgG(2),IgG(4)和IgE水平显着增加。 IgG(4)+ MOLPS患者的组织学标本显示明显的IgG(4)+浆细胞浸润。 IgG(4)+ MOLPS的许多患者都有淋巴细胞卵泡的形成,但淋巴上皮病变很少。典型SS患者的组织中几乎看不到IgG(4)+细胞。 38名接受糖皮质激素治疗的IgG(4)+ MOLPS患者表现出明显的临床改善。结论:尽管受累器官相似,但IgG(4)+ MOLPS和SS之间存在相当大的临床和病理学差异。基于临床特征和对糖皮质激素的良好反应,我们提出了一个新的临床实体:IgG(4)+ MOLPS。

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