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IgG4 相关疾病的免疫生物学和临床特征。

The immunobiology and clinical characteristics of IgG4 related diseases.

机构信息

First Department of Internal Medicine, Sapporo Medical University School of Medicine, South-1, West-16, Chuo-ku, Sapporo, Hokkaido 060-8543, Japan.

出版信息

J Autoimmun. 2012 Aug;39(1-2):93-6. doi: 10.1016/j.jaut.2012.01.007. Epub 2012 Feb 15.

Abstract

Having the characteristic features of elevated serum IgG4 levels and prominent infiltration of IgG4-positive plasma cells with fibrosis in lesions, Mikulicz's disease (MD) has been recognized as an IgG4-related disease (IgG4-RD). Although incidence of autoimmune pancreatitis (AIP), one of the organ characteristics of IgG4-RD, has been internationally reported, there are only a few such reports of IgG4-related MD. The limited number of reports might be attributable to the low recognition of IgG4-related MD as a clinical entity as well as its misdiagnosis as Sjögren's syndrome (SS). Thus, we compared several clinical features of MD with SS to improve proper clinical diagnosis of MD in the clinical setting. A total of 70 SS and 70 MD cases evaluated at Sapporo Medical University Hospital were retrospectively analyzed. In SS patients, sicca symptoms were the most frequent (87%), followed by articular symptoms (23%), while lacrimal and salivary gland swelling were a rare (10%) and transient manifestation. In contrast, lacrimal or salivary gland swelling was observed in all patients with MD. Although nearly 60% of MD patients complained of sicca syndrome, skin rash and arthralgia were rare symptoms. Hypergammaglobulinemia was recognized in both SS and MD patients, but the occurrence of autoantibodies in patients with IgG4-related MD was low. Extraglandular organ involvement, often involving the retroperitoneum, pancreas, kidney and lung, was often discovered at the time of IgG4-related MD diagnosis. Although corticosteroid therapy tended to delay the hypofunction of salivary gland in SS patients, recovery of decreased function of salivary glands were observed in IgG4-related MD patients. These results suggest the beneficial effect of aggressive corticosteroid intervention in patients with IgG4-related MD. Although SS and MD are both chronic inflammatory diseases affecting the lacrimal and salivary glands, their clinical features and corticosteroid responsiveness are different. Thus, differential diagnosis of these conditions is warranted.

摘要

米库利茨病(MD)具有血清 IgG4 水平升高和病变中 IgG4 阳性浆细胞浸润伴纤维化的特征,已被认为是一种 IgG4 相关疾病(IgG4-RD)。尽管 IgG4-RD 的器官特征之一——自身免疫性胰腺炎(AIP)的发病率已在国际上报道,但 IgG4 相关 MD 的报道却很少。报告数量有限的原因可能是由于 IgG4 相关 MD 作为一种临床实体的认识不足以及误诊为干燥综合征(SS)。因此,我们比较了 MD 与 SS 的几种临床特征,以提高 MD 在临床环境中的正确诊断。回顾性分析了在札幌医科大学医院评估的 70 例 SS 和 70 例 MD 病例。在 SS 患者中,口干症状最常见(87%),其次是关节症状(23%),而泪腺和唾液腺肿胀则很少见(10%)且为一过性表现。相比之下,所有 MD 患者均出现泪腺或唾液腺肿胀。尽管近 60%的 MD 患者有干燥综合征,但皮疹和关节炎是罕见的症状。SS 和 MD 患者均存在高丙种球蛋白血症,但 IgG4 相关 MD 患者自身抗体的发生率较低。IgG4 相关 MD 诊断时常发现胰腺、肾脏和肺部等外分泌腺器官受累。虽然皮质类固醇治疗可能会延迟 SS 患者唾液腺功能减退,但 IgG4 相关 MD 患者的唾液腺功能减退得到恢复。这些结果表明在 IgG4 相关 MD 患者中,积极的皮质类固醇干预具有有益作用。虽然 SS 和 MD 都是影响泪腺和唾液腺的慢性炎症性疾病,但它们的临床特征和皮质类固醇反应性不同。因此,需要对这些疾病进行鉴别诊断。

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