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阿巴西普用于原位肝移植术后移植物抗宿主病:一例报告

Abatacept use in graft-versus-host disease after orthotopic liver transplantation: a case report.

作者信息

Elfeki M A, Genco P V, Pungpapong S, Nakhleh R E, Nguyen J H, Harnois D M

机构信息

Department of Transplantation, Mayo Clinic Florida, Jacksonville, Florida.

Department of Transplantation, Mayo Clinic Florida, Jacksonville, Florida.

出版信息

Transplant Proc. 2014 Sep;46(7):2422-5. doi: 10.1016/j.transproceed.2014.06.061.

Abstract

BACKGROUND

Graft-versus-host disease (GVHD) is a rare, serious, fatal disease that occurs after orthotopic liver transplantation (OLT).

CASE REPORT

We treated a 60-year-old man who underwent OLT owing to familial amyloidosis. The patient developed fever on postoperative day 16. The fever was persistent and did not respond to antibiotic therapy. Cultures and radiologic studies were done and excluded infection as a potential cause. On postoperative day 26, a skin rash appeared on his chest, accompanied by diarrhea and persistent fever. The rash spread all over the trunk, neck, and arms, but spared the palms of his hands and soles of his feet. In the meantime, his blood cell count revealed pancytopenia. Skin biopsy was done and showed interface lymphocytic infiltrate that are largely centered on the dermal-epidermal junction, is consistent with GVHD (this pattern of rash distribution is unique and different from the rash of GVHD after hematopoietic stem cell transplant, which is confined to palms of the hands and soles of the feet; Fig 1). The diagnosis was confirmed by colonoscopy and multiple forceps biopsies, which revealed extensive crypt loss. After hematology consultation, the patient was treated by withdrawal of all immunosuppressive therapy coupled with abatacept infusion. Abatacept is a chimeric protein that inhibits T-lymphocytes and is approved by the US Food and Drug Administration for the treatment of rheumatoid arthritis. Interestingly, after second dose of abatacept the patient showed marked clinical and laboratory improvement. The patient was discharged after 47 days in a stable condition.

CONCLUSION

Because of the lack of a consensus for treatment of these patients, we report our experience with a male patient who had post-OLT GVHD and showed a marked improvement in response to abatacept.

摘要

背景

移植物抗宿主病(GVHD)是原位肝移植(OLT)后发生的一种罕见、严重且致命的疾病。

病例报告

我们治疗了一名因家族性淀粉样变性接受OLT的60岁男性患者。患者在术后第16天出现发热。发热持续存在,抗生素治疗无效。进行了培养和影像学检查,排除了感染作为潜在病因。术后第26天,他的胸部出现皮疹,伴有腹泻和持续发热。皮疹蔓延至整个躯干、颈部和手臂,但手掌和脚底未受累。与此同时,他的血细胞计数显示全血细胞减少。进行了皮肤活检,显示界面淋巴细胞浸润,主要集中在真皮 - 表皮交界处,符合GVHD(这种皮疹分布模式独特,与造血干细胞移植后GVHD的皮疹不同,后者局限于手掌和脚底;图1)。结肠镜检查和多次钳取活检证实了诊断,显示广泛的隐窝缺失。血液学会诊后,患者接受了停用所有免疫抑制治疗并联合输注阿巴西普的治疗。阿巴西普是一种抑制T淋巴细胞的嵌合蛋白,已获美国食品药品监督管理局批准用于治疗类风湿关节炎。有趣的是,在第二次输注阿巴西普后,患者在临床和实验室检查方面均有明显改善。患者在47天后病情稳定出院。

结论

由于对于这些患者的治疗缺乏共识,我们报告了一名OLT后发生GVHD的男性患者的治疗经验,该患者对阿巴西普治疗反应显著改善。

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