Urticaria with immunoglobulin G4-related disease: An association or coincidence?

Nemmar Chandra shekarabhatta Sahana, Shilpa Kanathur, A. Shanmukhappa, T. Revathi
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Abstract

Immunoglobulin (Ig) G4-related disease is a recently described fibro-inflammatory disease with diverse clinical manifestations but consistent and characteristic histopathological features across multiple organ systems and skin, leading to tissue sclerosis and ultimately organ failure if not treated adequately. Here, we report a case of 56-year-old male patient presenting with urticarial lesions and generalized itching for 4 months. Routine investigations showed elevated 24-h urine protein, absolute eosinophil count, serum IgE, reversed albumin: globulin ratio, and “M” spike on serum electrophoresis. Renal biopsy showed storiform fibrosis, diffuse dense inflammatory cells (plasma cells and eosinophils), and IgG4-positive cells on immunohistochemistry which was histologically highly suggestive of IgG4-related chronic tubulointerstitial nephritis. Quick response was seen with oral corticosteroids.
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荨麻疹与免疫球蛋白g4相关疾病:是关联还是巧合?
免疫球蛋白(Ig) g4相关疾病是最近发现的一种纤维炎症性疾病,具有多种临床表现,但在多器官系统和皮肤上具有一致和特征性的组织病理学特征,如果治疗不当,可导致组织硬化并最终导致器官衰竭。在此,我们报告一位56岁男性病患,表现为荨麻疹病变及全身瘙痒4个月。常规检查显示24小时尿蛋白升高,嗜酸性粒细胞绝对计数,血清IgE,白蛋白:球蛋白比逆转,血清电泳显示“M”尖峰。肾活检示层状纤维化,弥漫性致密炎性细胞(浆细胞和嗜酸性粒细胞),免疫组化显示igg4阳性细胞,组织学高度提示igg4相关性慢性肾小管间质性肾炎。口服皮质类固醇反应迅速。
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