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一组移植受者的病例系列,这些受者尽管接受了免疫抑制治疗,但仍患上了炎症性肠病。

A case series of transplant recipients who despite immunosuppression developed inflammatory bowel disease.

作者信息

Riley T R, Schoen R E, Lee R G, Rakela J

机构信息

Department of Medicine, University of Pittsburgh, Pennsylvania, USA.

出版信息

Am J Gastroenterol. 1997 Feb;92(2):279-82.

PMID:9040206
Abstract

OBJECTIVES

We describe 14 patients who developed inflammatory bowel disease (IBD) after transplantation despite immunosuppression.

METHODS

Using an electronic medical archival retrieval system, records of 6800 liver and kidney transplant patients were searched for evidence of IBD. The pathology was reviewed, and infectious etiologies were excluded.

RESULTS

Fourteen patients developed IBD after transplantation. Twelve patients had undergone liver transplantation, and two kidney transplantation. Four had transplantation for autoimmune hepatitis; four for non-A, non-B, non-C hepatitis; two for primary sclerosing cholangitis; one for giant cell hepatitis; one for biliary atresia; one for polycystic kidney disease; and one for obstructive uropathy. Mean age at development of IBD was 38 yr. Mean time to development of IBD after transplantation was 4 yr. Endoscopically there were two cases limited to the left side, eight of pancolitis, of which one had terminal ileal disease, and four of patchy colitis. Histology was consistent with ulcerative colitis in nine patients and Crohn's disease in five. Patients with ulcerative colitis either responded and remained in remission on maintenance therapy (seven of nine) or were refractory and required a colectomy (two of nine). Patients with Crohn's disease continued to have flares despite treatment (five of five).

CONCLUSION

  1. New onset IBD can develop after solid organ transplantation, despite use of immunosuppressive therapy. 2) A full spectrum of IBD can be seen after transplantation. 3) Study of these patients could shed light on why immunosuppression is not uniformly effective for IBD and provide clues to the inflammatory determinants of IBD.
摘要

目的

我们描述了14例尽管接受了免疫抑制治疗但仍在移植后发生炎症性肠病(IBD)的患者。

方法

使用电子医疗档案检索系统,对6800例肝移植和肾移植患者的记录进行检索,以寻找IBD的证据。对病理进行了复查,并排除了感染性病因。

结果

14例患者在移植后发生IBD。12例患者接受了肝移植,2例接受了肾移植。4例因自身免疫性肝炎进行移植;4例因非甲、非乙、非丙型肝炎进行移植;2例因原发性硬化性胆管炎进行移植;1例因巨细胞肝炎进行移植;1例因胆道闭锁进行移植;1例因多囊肾病进行移植;1例因梗阻性尿路病进行移植。IBD发病时的平均年龄为38岁。移植后发生IBD的平均时间为4年。内镜检查发现,2例病变局限于左侧,8例为全结肠炎,其中1例有回肠末端病变,4例为斑片状结肠炎。组织学检查结果9例符合溃疡性结肠炎,5例符合克罗恩病。溃疡性结肠炎患者接受维持治疗后有的有反应并维持缓解状态(9例中的7例),有的无效且需要进行结肠切除术(9例中的2例)。克罗恩病患者尽管接受了治疗仍持续发作(5例中的5例)。

结论

1)尽管使用了免疫抑制治疗,但实体器官移植后仍可发生新发IBD。2)移植后可出现各种类型的IBD。3)对这些患者的研究可能有助于阐明为什么免疫抑制对IBD并非始终有效,并为IBD的炎症决定因素提供线索。

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