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小儿实体器官移植后的急性移植物抗宿主病

Acute graft-versus-host disease after pediatric solid organ transplant.

作者信息

Yashar Sharona, Wu Steven S, Binder Scott W, Cotliar Jonathan

机构信息

UCLA Department of Medicine, Division of Dermatology, Los Angeles, CA 90095-6957, USA.

出版信息

J Drugs Dermatol. 2008 May;7(5):467-9.

Abstract

Acute graft-versus-host disease (GVHD) is a rare and life threatening complication after solid organ transplantation. The diagnosis can be made with clinical and laboratory evidence of skin, liver, or intestinal involvement. The role of skin biopsy in confirming acute GVHD is debatable. However, it is proposed that the skin biopsy is a valuable tool in confirming the diagnosis in low prior probability settings. An atypical case of acute GVHD following orthotopic liver and small bowel transplantation in a 2-year-old male is presented. Seven weeks posttransplantation, the patient developed a bullous eruption limited to the buttocks and upper thighs. A skin biopsy was performed which showed interface dermatitis and epidermal necrosis consistent with acute GVHD. Prompt treatment with daclizumab and intravenous corticosteroids was given and the patient survived without evidence of systemic GVHD. This case highlights the importance of skin biopsy in establishing the prompt diagnosis of GVHD in low prior probability settings.

摘要

急性移植物抗宿主病(GVHD)是实体器官移植后一种罕见且危及生命的并发症。可根据皮肤、肝脏或肠道受累的临床及实验室证据做出诊断。皮肤活检在确诊急性GVHD中的作用存在争议。然而,有人提出皮肤活检在先前可能性较低的情况下是确诊的一种有价值的工具。本文介绍了一名2岁男性原位肝移植和小肠移植后发生急性GVHD的非典型病例。移植后7周,患者臀部和大腿上部出现大疱性皮疹。进行了皮肤活检,结果显示界面性皮炎和表皮坏死,符合急性GVHD表现。立即给予达利珠单抗和静脉注射皮质类固醇治疗,患者存活,未出现全身性GVHD迹象。该病例凸显了皮肤活检在先前可能性较低的情况下迅速诊断GVHD的重要性。

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