Nephrotic proteinuria and hematuria with newly diagnosed IgA nephropathy after liver transplant: A case report

IF 1.6 4区 医学 Q4 IMMUNOLOGY Transplant immunology Pub Date : 2024-01-23 DOI:10.1016/j.trim.2024.102003
Tingli Wang , Honghong Ren , Dan Yin , Hongyu Qiu
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Abstract

Background

IgA nephropathy is a renal lesion in patients with end-stage liver disease, called hepatic IgA nephropathy. The common manifestation of hepatic IgA nephropathy is microscopic hematuria. Sirolimus, often used to prevent organ rejection, has been reported to induce proteinuria after organ transplantation. But few cases of nephrotic proteinuria and hematuria are reported.

Case presentation

In this case, a 45-year-old male with a long history of hepatic B virus infection and liver cirrhosis, received liver transplant and was taking sirolimus as one of his immunosuppression drugs. Overt proteinuria and hematuria occurred. With no proteinuria history before, renal biopsy was performed, which indicated IgA nephropathy.

Conclusion

We reported a liver recipient, who was taking sirolimus, developing nephrotic proteinuria and hematuria with IgA nephropathy. Further studies need to be carried out to disclose mechanism behind this phenomenon.

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肝移植后新诊断的 IgA 肾病伴有肾病性蛋白尿和血尿:病例报告。
背景:IgA 肾病是终末期肝病患者的一种肾脏病变,称为肝性 IgA 肾病。肝IgA肾病的常见表现是镜下血尿。西罗莫司常用于预防器官排斥反应,有报道称其会在器官移植后诱发蛋白尿。但很少有肾病性蛋白尿和血尿的病例报道:在本病例中,一名 45 岁的男性接受了肝移植手术,并服用了西罗莫司作为免疫抑制剂之一,他有长期的肝 B 病毒感染和肝硬化病史。他出现了明显的蛋白尿和血尿。由于之前没有蛋白尿病史,他接受了肾活检,结果显示为 IgA 肾病:我们报告了一名服用西罗莫司的肝脏受者出现肾病性蛋白尿和血尿,并伴有IgA肾病。这一现象背后的机制还需要进一步研究。
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来源期刊
Transplant immunology
Transplant immunology 医学-免疫学
CiteScore
2.10
自引率
13.30%
发文量
198
审稿时长
48 days
期刊介绍: Transplant Immunology will publish up-to-date information on all aspects of the broad field it encompasses. The journal will be directed at (basic) scientists, tissue typers, transplant physicians and surgeons, and research and data on all immunological aspects of organ-, tissue- and (haematopoietic) stem cell transplantation are of potential interest to the readers of Transplant Immunology. Original papers, Review articles and Hypotheses will be considered for publication and submitted manuscripts will be rapidly peer-reviewed and published. They will be judged on the basis of scientific merit, originality, timeliness and quality.
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