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Biopsy-proven recurrence of unilateral IgG4-related orbital inflammation after 20 years

机译:经活组织检查证实20年后单侧IgG4相关的眼眶炎症复发

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A 38-year-old female patient presented with a painful swelling in the lateral part of the upper eyelid, a diffuse scleritis and slight hypoglobus of the right eye. An orbital biopsy showed a fibrotic idiopathic orbital inflammation (IOI) with, on immunohistochemical staining, an increased number of IgG4-positive plasma cells scored as >200 per high-power field, with IgG4/IgG ratio >0.50, indicating orbital IgG4 related autoimmune disease. On treatment with oral prednisone and azathioprine the symptoms resolved within 6 months. Twenty years prior, the patient had been diagnosed with an IOI of at the same side, for which at that time a biopsy had been taken similarly. Reclassification of the previous biopsy specimen with immunohistological staining also showed evidence of orbital IgG4 related disease. To our knowledge this is the first report of a biopsy-proven unilateral IgG4-related orbitopathy that recurred after 20 years.
机译:一名38岁的女性患者,上眼睑外侧出现疼痛性肿胀,弥漫性巩膜炎和右眼轻度眼球下降。眼眶活检显示为纤维化特发性眼眶炎(IOI),免疫组化染色显示,每个高倍视野评分大于200的IgG4阳性浆细胞数量增加,IgG4 / IgG比率大于0.50,表明与眼眶IgG4相关的自身免疫疾病。口服泼尼松和硫唑嘌呤治疗后,症状在6个月内消失。二十年前,该患者被诊断出同一侧的IOI,当时对此进行了类似的活检。用免疫组织学染色对先前的活检标本进行重新分类也显示了与眼眶IgG4相关疾病的证据。据我们所知,这是经活组织检查证实的单侧IgG4相关眼眶病的首次报道,该报道在20年后复发。

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