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IgA 血管炎(过敏性紫癜)

IgA Vasculitis (Henoch-Schönlein Purpura)

作者信息

Roache-Robinson Porsha, Killeen Robert B., Hotwagner David T.

机构信息

PBGGME/St. Lucie Medical Center

University of Illinois

Abstract

Immunoglobulin A vasculitis (IgAV), formerly Henoch-Schönlein purpura, involves the small vessels of the joints, kidneys, gastrointestinal tract, and skin. IgAV can also affect the central nervous system and the lungs; however, these findings are rare. It is an acute IgA-mediated disorder typically self-limited and managed with supportive care; however, serious complications, such as renal failure, can occur. Henoch-Schönlein purpura is named after the German physician, Dr. Johann Schönlein and his student Eduard Henoch. Schönlein identified the association between joint pain and purpura, and Henoch identified gastrointestinal and renal involvement. Although Henoch-Schönlein purpura is named after Henoch and Schönlein, an English physician named William Heberden was the first to describe the disorder in the early 1800s. Iga vasculitis is now the preferred term due to a tendency toward etiology-based rather than eponym-based nomenclature. Of note, IgA vasculitis with nephritis has many overlapping features with IgA nephropathy, which is the most common glomerulonephritis in the world. The primary differences are that IgAV with nephritis is more likely to first occur in children younger than 15, while IgA nephropathy usually has an onset in patients older than 15. IgAV with nephritis is more likely to present with extrarenal symptoms; IgA nephropathy presents more often with gross hematuria. Histology in IgAV with nephritis shows more capillary staining and glomerular injury than in IgA nephropathy. Finally, IgAV with nephritis has a 98% clinical remission; comparatively, patients with IgA nephropathy progress to end-stage renal disease within 20 years of diagnosis in 30% to 50% of cases. Another interesting difference is that IgAV with nephritis presents more often during the winter "cold" season, while IgA nephropathy does not show seasonality. Much of the difference between the two disease processes results from IgAV being predominantly a disease of children and IgA nephropathy being primarily a disease of adults.

摘要

免疫球蛋白A血管炎(IgAV),以前称为过敏性紫癜,累及关节、肾脏、胃肠道和皮肤的小血管。IgAV也可影响中枢神经系统和肺部;然而,这些表现较为罕见。它是一种急性IgA介导的疾病,通常为自限性疾病,采用支持性治疗;然而,可能会出现严重并发症,如肾衰竭。过敏性紫癜以德国医生约翰·舍恩莱因博士及其学生爱德华·海涅克的名字命名。舍恩莱因确定了关节疼痛与紫癜之间的关联,海涅克确定了胃肠道和肾脏受累情况。尽管过敏性紫癜以海涅克和舍恩莱因的名字命名,但一位名叫威廉·赫伯登的英国医生在19世纪初首次描述了这种疾病。由于倾向于基于病因的命名而非基于人名的命名,IgA血管炎现在是首选术语。值得注意的是,IgA血管炎伴肾炎与IgA肾病有许多重叠特征,IgA肾病是世界上最常见的肾小球肾炎。主要区别在于,IgA血管炎伴肾炎更易首次发生于15岁以下儿童,而IgA肾病通常在15岁以上患者中发病。IgA血管炎伴肾炎更易出现肾外症状;IgA肾病更常表现为肉眼血尿。IgA血管炎伴肾炎的组织学表现比IgA肾病有更多的毛细血管染色和肾小球损伤。最后,IgA血管炎伴肾炎的临床缓解率为98%;相比之下,IgA肾病患者在诊断后20年内有30%至50%的病例进展为终末期肾病。另一个有趣的区别是,IgA血管炎伴肾炎在冬季“寒冷”季节更常出现,而IgA肾病没有季节性。这两种疾病过程的许多差异是由于IgA血管炎主要是儿童疾病,而IgA肾病主要是成人疾病。

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