首页> 外文期刊>Medicine. >Clinical and morphologic spectrum of renal involvement in patients with mixed cryoglobulinemia without evidence of hepatitis C virus infection.
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Clinical and morphologic spectrum of renal involvement in patients with mixed cryoglobulinemia without evidence of hepatitis C virus infection.

机译:没有丙型肝炎病毒感染证据的混合性冷球蛋白血症患者肾脏受累的临床和形态学频谱。

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摘要

Hepatitis C virus (HCV) infection represents, by far, the major cause of mixed cryoglobulinemia (MC). The renal disease associated with this pathological condition is now well described. By contrast, renal involvement in patients with MC not associated with HCV has been only poorly described, and few cases have been reported. We analyzed the demographic, clinical, and laboratory features and outcome in patients presenting with renal disease associated with MC not related to HCV infection. Records of 20 patients with MC and renal disease, with no evidence of HCV by serology and polymerase chain reaction analysis, were retrospectively analyzed. Renal biopsies and extensive searches for lymphoproliferative disorder were performed in all patients at presentation. MC was related to primary Sjogren Syndrome (pSS) in 9 patients, and to non-Hodgkin lymphoma in 1 patient, while MC was classified as essential in the remaining 10 cases. Renal involvement was characterized by microscopic hematuria in all patients, nephrotic range proteinuria in 75% of patients, hypertension in 80% of patients, and renal failure in 85% of patients (mean glomerular filtration rate, 46 mL/min per 1.73 m). Membranoproliferative glomerulonephritis with subendothelial deposits was observed in all kidney specimens. Skin vasculitis was the main extrarenal manifestation. In all patients, cryoglobulinemia was classified as type II MC, characterized by monoclonal IgMkappa and polyclonal IgG. Most patients (17/20) were treated with steroids or immunosuppressive agents, or both. Initial renal remission was observed in 94% of patients. However, renal relapse occurred in most patients, with 10% reaching end-stage renal disease. Three patients with essential MC developed B-cell lymphoma 36-48 months after the diagnosis of MC. Unexpectedly, B-cell lymphoma induced by Epstein-Barr virus infection occurred in only 1 of the 9 pSS patients. Forty percent of patients died as a result of extrarenal causes.Renal disease associated with MC unrelated to HCV is characterized by the high prevalence of pSS (45%), the finding of CD20+ B-lymphocyte nodular infiltrates in the kidney interstitium, and a high incidence of overt B-cell lymphoma during follow-up. These findings emphasize the need for repetitive clinical evaluation in those patients.
机译:到目前为止,丙型肝炎病毒(HCV)感染是混合性冷球蛋白血症(MC)的主要原因。现在已经很好地描述了与这种病理状况有关的肾脏疾病。相比之下,与HCV不相关的MC患者的肾脏受累仅描述不清,很少报道。我们分析了患有与HCV感染无关的MC相关肾病的患者的人口统计学,临床和实验室特征及结局。回顾性分析了20例MC和肾脏疾病患者的病历,这些患者没有血清学和聚合酶链反应分析的HCV证据。所有的患者均进行了肾脏活检和广泛的淋巴增生性疾病检查。 MC与9例原发性干燥综合征(pSS)相关,与1例与非霍奇金淋巴瘤相关,而在其余10例中,MC被分类为必不可少的。肾脏受累的特点是所有患者均出现镜下血尿,75%的患者患有肾病范围蛋白尿,80%的患者患有高血压,85%的患者患有肾衰竭(平均肾小球滤过率,每1.73 m为46 mL / min)。在所有肾脏标本中均观察到膜增生性肾小球肾炎伴内皮下沉积。皮肤血管炎是主要的肾外表现。在所有患者中,冷球蛋白血症被分类为II型MC,其特征是单克隆IgMkappa和多克隆IgG。大多数患者(17/20)均接受类固醇或免疫抑制剂或两者同时治疗。 94%的患者观察到最初的肾脏缓解。但是,大多数患者发生肾脏复发,其中有10%达到终末期肾脏疾病。三名原发性MC患者在诊断MC后36-48个月发展为B细胞淋巴瘤。出乎意料的是,由爱泼斯坦-巴尔病毒感染引起的B细胞淋巴瘤仅发生在9例pSS患者中的1例中。 40%的患者因肾外原因死亡。与HCV无关的MC所致的肾脏疾病的特征是pSS的患病率高(45%),在肾脏间质中发现CD20 + B淋巴细胞结节浸润,随访期间明显的B细胞淋巴瘤的发病率。这些发现强调了对这些患者进行重复临床评估的必要性。

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