异体造血细胞移植治疗镰状细胞病后炎症性肠病。

IF 2.3 3区 医学 Q2 HEMATOLOGY
Emily Rowland, Akshay Sharma, Samantha Paglinco, Ross M Maltz, Jeffrey E Deyo, Kiran Joglekar, John Brannon Alberty, Courtney Fitzhugh, Hemalatha G Rangarajan
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引用次数: 0

摘要

虽然移植物抗宿主病(GvHD)是异基因造血干细胞移植(HCT)后胃肠道(GI)并发症的重要原因,但非特异性症状使诊断具有挑战性。我们描述了3例镰状细胞病患者,他们在hct后4-18个月出现炎症性肠病(IBD)样表现。所有患者均接受外周血干细胞移植和西罗莫司预防GvHD。所有患者均有慢性腹泻,活检显示广泛的结肠溃疡,非坏死性肉芽肿,GvHD的组织学证据很少。通过ibd定向治疗,症状迅速缓解。我们的报告强调了考虑HCT后胃肠道并发症(如IBD)的其他罕见病因的重要性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Inflammatory Bowel Disease Following Allogeneic Hematopoietic Cell Transplant for Sickle Cell Disease.

Although graft-versus-host disease (GvHD) is an important cause of gastrointestinal (GI) complications after allogeneic hematopoietic stem cell transplantation (HCT), the non-specific symptoms make diagnosis challenging. We described three patients with sickle cell disease who developed inflammatory bowel disease (IBD) like manifestations 4-18 months post-HCT. All patients received peripheral blood stem cell grafts and sirolimus for GvHD prophylaxis. All had chronic diarrhea, and biopsies showed extensive colonic ulceration, non-necrotizing granulomas, with minimal histologic evidence of GvHD. Symptoms resolved promptly with IBD-directed therapy. Our report highlights the importance of considering alternative rare etiologies for GI complications such as IBD after HCT.

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来源期刊
Pediatric Blood & Cancer
Pediatric Blood & Cancer 医学-小儿科
CiteScore
4.90
自引率
9.40%
发文量
546
审稿时长
1.5 months
期刊介绍: Pediatric Blood & Cancer publishes the highest quality manuscripts describing basic and clinical investigations of blood disorders and malignant diseases of childhood including diagnosis, treatment, epidemiology, etiology, biology, and molecular and clinical genetics of these diseases as they affect children, adolescents, and young adults. Pediatric Blood & Cancer will also include studies on such treatment options as hematopoietic stem cell transplantation, immunology, and gene therapy.
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