肉芽肿伴多血管炎:诱因不能长期隐藏。

IF 1.3 Q4 RHEUMATOLOGY European journal of rheumatology Pub Date : 2022-01-01 DOI:10.5152/eurjrheum.2021.21093
Shameek Gayen, Diana Zhang, Eliza Sternlicht, Daniel Bulanowski, Maher Tabba
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引用次数: 1

摘要

肉芽肿病伴多血管炎(GPA)是一种血管炎,可累及多个器官,尤其是呼吸道和肾脏。临床表现和抗中性粒细胞细胞质抗体血清滴度升高怀疑诊断,病变器官活检证实。病毒感染已被描述为免疫系统在发展GPA的触发因素之一。在这个报告中,我们描述了一个罕见的病例,在巨细胞病毒感染后发展为GPA,患者免疫功能不全。
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Granulomatosis with polyangiitis: The trigger cannot be long hidden.

Granulomatosis with polyangiitis, or GPA, is a form of vasculitis that affects multiple organs especially the respiratory tract and the kidneys. The diagnosis is suspected with the clinical presentation and elevated serum titer of antineutrophil cytoplasmic antibodies and confirmed with the biopsy of the affected organ. Viral infection has been described as one of the triggers of the immune system in developing GPA. In this report, we describe a rare case of GPA that developed following cytomegalovirus infection in a patient with unknown immunocompromised medical condition.

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