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混合性冷球蛋白血症患者获得性范可尼综合征:单中心病例系列。

Acquired Fanconi syndrome in mixed cryoglobulinemia patients: a single-center case series.

机构信息

Department of Nephrology, Peking Union Medical College Hospital, Chinese Academy of Medical Sciences, Beijing, 100730, People's Republic of China.

4 + 4 Medical Doctor Program, Chinese Academy of Medical Sciences & Peking Union Medical College, Beijing, 100730, People's Republic of China.

出版信息

Clin Rheumatol. 2024 Jul;43(7):2329-2336. doi: 10.1007/s10067-024-06997-2. Epub 2024 May 10.

Abstract

PURPOSE

Cryoglobulinemia is a pathological condition characterized by the presence of cryoglobulins in the blood, with cryoglobulinemic glomerulonephritis being the most frequent form of renal involvement. Fanconi syndrome presents as a generalized dysfunction of the proximal tubule, characterized by the presence of polyuria, phosphaturia, glycosuria, proteinuria, proximal renal tubular acidosis, and osteomalacia. We aimed to present five cases co-occurring with Fanconi syndrome and cryoglobulinemia.

METHODS

We retrospectively summarized the cases of five patients with Fanconi syndrome and cryoglobulinemia at Peking Union Medical College Hospital from January 2012 to June 2022. The clinical features, diagnosis, treatment, and prognosis were systematically analyzed.

RESULTS

All five patients exhibited typical features of Fanconi syndrome, and cryoglobulinemia was concurrently detected in all cases. These patients also exhibit positive anti-nuclear antibody spectrum and hyperglobulinemia, and IgM constitutes the predominant monoclonal component in cryoglobulins. In addition to supplemental treatment, timely immunosuppressive therapy may potentially benefit the long-term renal prognosis of patients with this condition.

CONCLUSION

Our findings highlight the rare co-occurrence of Fanconi syndrome and cryoglobulinemia in clinical practice. Despite the lack of causal evidence, the coexistence of Fanconi syndrome and tubulointerstitial injury is also noteworthy in patients with cryoglobulinemia, underscoring the importance of thorough evaluation and tailored management in patients presenting with overlapping renal manifestations. Key Points • Patients with mixed cryoglobulinemia can clinically present with tubulointerstitial injury, specifically manifesting as Fanconi syndrome. • In addition to typical symptoms of Fanconi syndrome, these patients also exhibit positive anti-nuclear antibody spectrum and hyperglobulinemia, while IgM constitutes the monoclonal component in cryoglobulins. • Timely immunosuppressive therapy may improve long-term renal prognosis in these patients.

摘要

目的

冷球蛋白血症是一种以血液中存在冷球蛋白为特征的病理状态,其中冷球蛋白血症性肾小球肾炎是最常见的肾受累形式。范可尼综合征表现为近端肾小管的广泛功能障碍,其特征为多尿、磷酸盐尿、糖尿、蛋白尿、近端肾小管酸中毒和佝偻病。我们旨在介绍 5 例同时伴有范可尼综合征和冷球蛋白血症的病例。

方法

我们回顾性总结了 2012 年 1 月至 2022 年 6 月期间北京协和医院收治的 5 例范可尼综合征合并冷球蛋白血症患者的病例。系统分析了这些患者的临床特征、诊断、治疗和预后。

结果

所有 5 例患者均表现出典型的范可尼综合征特征,且所有患者均同时检测出冷球蛋白血症。这些患者还表现出抗核抗体谱阳性和高球蛋白血症,冷球蛋白中的主要单克隆成分是 IgM。除了补充治疗外,及时的免疫抑制治疗可能对患者的长期肾脏预后有益。

结论

我们的研究结果强调了范可尼综合征和冷球蛋白血症在临床实践中罕见的同时发生。尽管缺乏因果关系的证据,但在冷球蛋白血症患者中,范可尼综合征和肾小管间质损伤的共存也值得注意,这强调了在出现重叠肾脏表现的患者中进行彻底评估和个体化管理的重要性。

关键点

  • 混合性冷球蛋白血症患者可出现肾小管间质损伤,表现为范可尼综合征。

  • 除了典型的范可尼综合征症状外,这些患者还表现出抗核抗体谱阳性和高球蛋白血症,冷球蛋白中的单克隆成分是 IgM。

  • 及时的免疫抑制治疗可能改善这些患者的长期肾脏预后。

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