富浆细胞肾炎伴全身性多克隆淋巴增生性疾病,模拟特发性多中心Castleman病、系统性红斑狼疮和igg4相关疾病

IF 1 4区 医学 Q3 MEDICINE, GENERAL & INTERNAL
Yu Hebisawa, Akihito Ohta, Ryutaro Sekimoto, Natsuko Sakurai, Keigo Setoguchi
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引用次数: 0

摘要

特发性多中心Castleman病(iMCD)、系统性红斑狼疮(SLE)和igg4相关疾病(IgG4-RD)可引起累及肾脏的淋巴结病。由于没有确定诊断这些疾病的金标准,因此可以通过排除其他疾病来进行诊断。然而,有些病例很难确诊。60岁男性,以淋巴结病、肾功能不全、补体不足为主要表现。怀疑为自身免疫性胰腺炎和iMCD。肾活检显示免疫复合物介导的肾小球肾炎叠加内皮损伤和富含浆细胞的小管间质肾炎伴层状纤维化。虽然存在iMCD、SLE和IgG4-RD的特征,但无法明确分类。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Plasma Cell-rich Nephritis with a Systemic Polyclonal Lymphoproliferative Disorder, Mimicking Idiopathic Multicentric Castleman Disease, Systemic Lupus Erythematosus, and IgG4-related Disease.

Idiopathic multicentric Castleman disease (iMCD), systemic lupus erythematosus (SLE), and IgG4-related disease (IgG4-RD) can cause lymphadenopathy with renal involvement. As no gold standards have been set for diagnosing these conditions, diagnoses can be made by excluding other conditions. However, some cases are difficult to identify. A 60-year-old man presented with lymphadenopathy, renal dysfunction, and hypocomplementemia. Autoimmune pancreatitis and iMCD had been suspected. A renal biopsy revealed immune complex-mediated glomerulonephritis superimposed on endothelial injury and plasma cell-rich tubulointerstitial nephritis with storiform-like fibrosis. While the features of iMCD, SLE, and IgG4-RD were present, a clear classification could not be achieved.

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来源期刊
Internal Medicine
Internal Medicine 医学-医学:内科
CiteScore
1.90
自引率
8.30%
发文量
0
审稿时长
2.2 months
期刊介绍: Internal Medicine is an open-access online only journal published monthly by the Japanese Society of Internal Medicine. Articles must be prepared in accordance with "The Uniform Requirements for Manuscripts Submitted to Biomedical Journals (see Annals of Internal Medicine 108: 258-265, 1988), must be contributed solely to the Internal Medicine, and become the property of the Japanese Society of Internal Medicine. Statements contained therein are the responsibility of the author(s). The Society reserves copyright and renewal on all published material and such material may not be reproduced in any form without the written permission of the Society.
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