Massive Intestinal Bleeding in an Adult with IgA Vasculitis Treated with Intravenous Immunoglobulin.

Case Reports in Rheumatology Pub Date : 2022-06-14 eCollection Date: 2022-01-01 DOI:10.1155/2022/9694911
Ibrahim Nassereddin, Ariel Kenig, Yuval Ishay, Hillel Lehmann, Noa Hurvitz, Narmine Elkhateeb, Ram Gelman, Yael Ratz, Inon Sarig, Ido Burstain, Stephanie Benshushan, Fadi Kharouf
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引用次数: 1

Abstract

We report the case of a 29-year-old adult presenting with severe IgA vasculitis, with cutaneous, urologic, and renal manifestations. The late appearance of severe gastrointestinal bleeding dominated the clinical picture, necessitating the administration of tens of units of packed cells and the augmentation of the immunosuppressive protocol. It was not until therapy with intravenous immunoglobulin (IVIG) was introduced that the massive bleeding was controlled. We herein discuss the patient's presentation, the gastrointestinal manifestations of IgA vasculitis, the recommended treatments, and the existent evidence about IVIG therapy.

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静脉注射免疫球蛋白治疗成人IgA血管炎大出血1例。
我们报告的情况下,29岁的成人提出严重的IgA血管炎,与皮肤,泌尿系统和肾脏的表现。晚期出现的严重胃肠道出血在临床表现中占主导地位,需要使用数十个单位的堆积细胞和增强免疫抑制方案。直到静脉注射免疫球蛋白(IVIG)治疗,大出血才得到控制。我们在此讨论患者的表现,IgA血管炎的胃肠道表现,推荐的治疗方法,以及现有的IVIG治疗证据。
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审稿时长
12 weeks
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