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狼疮患者假性假性梅格斯综合征所致高血铁蛋白血症可引起严重炎症:两例病例报告及文献复习。

Severe inflammation may be caused by hyperferritinemia of pseudo-pseudo Meigs' syndrome in lupus patients: two cases reports and a literature review.

出版信息

Clin Rheumatol. 2013 Dec;32(12):1823-6. doi: 10.1007/s10067-013-2362-8.

Abstract

Pseudo-pseudo Meigs' syndrome or Tjalma syndrome is a rare manifestation of patients with systemic lupus erythematosus defined by the presence of ascites, pleural effusions, and an elevated cancer antigen 125 level. In this case, we described a patient with lupus who presented with sudden impaired renal function and subsequent development of massive ascites with marked high serum ferritin. Hyperferritinemia is one of the abnormal laboratory findings in severe inflammation with ferritin functioning as an inflammatory marker. However, its correlation with lupus activity remains unclear. Therefore, a review of the literature regarding pseudo-pseudo Meigs' syndrome associated with lupus and high ferritin level in this disease was carried out.

摘要

假性假性梅格斯综合征或 Tjalma 综合征是一种罕见的系统性红斑狼疮表现,其特征为腹水、胸腔积液和癌抗原 125 水平升高。在本例中,我们描述了一名狼疮患者,其表现为肾功能突然受损,随后出现大量腹水,血清铁蛋白显著升高。高血清铁蛋白血症是严重炎症的异常实验室发现之一,铁蛋白作为炎症标志物发挥作用。然而,其与狼疮活动的相关性尚不清楚。因此,对与狼疮相关的假性假性梅格斯综合征以及该病中高铁蛋白水平的文献进行了回顾。

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