原发性斯约格伦综合征的两种并发罕见腺外表现:IgA 肾病和自身免疫性肝炎

Q4 Medicine
Mediterranean Journal of Rheumatology Pub Date : 2024-01-29 eCollection Date: 2024-06-01 DOI:10.31138/mjr.260123.ina
Rashmi Roongta, Sonali Dey, Sumantro Mondal, Alakendu Ghosh
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引用次数: 0

摘要

原发性斯约格伦综合征(pSS)是一种全身性自身免疫性疾病,很少会出现多种腺外表现。我们在此报告了一例以 IgA 肾病和自身免疫性肝炎为首发表现的 pSS 患者。她表现为多关节痛、眼部症状和持续性乏力,但无肾脏和肝脏受累症状。自身免疫性疾病可能有重叠的临床特征,偶尔也会表现出非特异性症状,导致诊断延误。因此,必须对所有 pSS 患者进行全面评估,以便及早识别多种多样的腺体外特征,并启动及时治疗以改善预后。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Two Concomitant Rare Extraglandular Manifestations of Primary Sjögren's Syndrome: IgA Nephropathy and Autoimmune Hepatitis.

Primary Sjögren's syndrome (pSS) is a systemic autoimmune disease and can rarely present with multiple extraglandular manifestations. Here we report a case of pSS with concomitant IgA nephropathy and autoimmune hepatitis as the initial manifestations. She presented with polyarthralgia, sicca symptoms and persistent fatigue but was asymptomatic for renal and liver involvement. Autoimmune diseases can have overlapping clinical features and occasionally, manifest nonspecific symptoms leading to delay in diagnosis. It is therefore imperative to thoroughly evaluate any patient of pSS for early recognition of the diverse extraglandular features and initiate prompt treatment to improve outcome.

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来源期刊
CiteScore
2.00
自引率
0.00%
发文量
42
审稿时长
8 weeks
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