Suppr超能文献

联体肠肾移植治疗包裹性腹膜硬化症 1 例报告

Combined intestine and kidney transplantation in a patient with encapsulating peritoneal sclerosis: case report.

机构信息

Digestive Disease Institute, Cleveland Clinic Foundation, Cleveland, OH.

出版信息

Am J Transplant. 2013 Dec;13(12):3274-7. doi: 10.1111/ajt.12505. Epub 2013 Nov 13.

Abstract

Encapsulating peritoneal sclerosis (EPS) is a rare but devastating complication of peritoneal dialysis characterized by fibrosis and calcification of the intestine that, in severe cases, can progress to intestinal failure and total parenteral nutrition dependency. Medical and surgical interventions carry a poor prognosis in these patients. We describe a case of a 36-year-old female with end-stage kidney disease and severe EPS not amenable to surgical intervention who underwent a combined intestinal and kidney transplantation. At 3 years posttransplantation, the patient has normal intestinal and kidney function. This represents, to our knowledge, the first report of severe EPS and end-stage kidney disease treated with a combined transplant.

摘要

包裹性腹膜硬化症(EPS)是腹膜透析的一种罕见但严重的并发症,其特征为肠纤维化和钙化,在严重的情况下,可进展为肠衰竭和完全胃肠外营养依赖。在这些患者中,医学和手术干预的预后较差。我们描述了一例 36 岁女性终末期肾病和严重的 EPS 病例,该患者不适宜手术干预,接受了肠肾联合移植。移植术后 3 年,患者的肠和肾功能正常。据我们所知,这是首例采用联合移植治疗严重 EPS 和终末期肾病的报告。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验