Hammami Muhammad Bader, Al-Taee Ahmad, Meeks Marshall, Fesler Mark, Hurley M Yadira, Cao Dengfeng, Lai Jin-Ping
Division of Gastroenterology and Hepatology, Department of Internal Medicine, Saint Louis University School of Medicine, 1402 S. Grand Blvd., St Louis, MO, 63104, USA.
Department of Internal Medicine, Saint Louis University School of Medicine, St. Louis, MO, USA.
Clin J Gastroenterol. 2017 Apr;10(2):142-146. doi: 10.1007/s12328-016-0707-y. Epub 2016 Dec 26.
Idelalisib is a selective inhibitor of the delta isoform of phosphatidylinositol 3-kinase which was approved by the United States Federal Drug Administration in 2014 for the treatment of relapsed chronic lymphocytic leukemia and indolent non-Hodgkin lymphoma. Drug-induced injury of the gastrointestinal tract is a relatively frequent but usually under-recognized disease entity.
We report the case of a 56-year-old male with a history of relapsed follicular lymphoma status post allogenic bone marrow transplant who developed severe diarrhea with a skin eruption mimicking graft-versus-host disease (GVHD) 6 months after starting idelalisib. He underwent a colonoscopy demonstrating a grossly normal-appearing colon and terminal ileum. Biopsies taken during the procedure revealed mild active ileitis, colitis, and proctitis with frequent epithelial apoptosis, and focal intra-epithelial lymphocytosis. Skin biopsies revealed sub-acute spongiotic dermatitis suggestive of either contact dermatitis or an eczematous drug reaction. Symptoms were attributed to idelalisib given their resolution with withdrawal of the drug in conjunction with the skin and colonic biopsies.
High clinical suspicion and awareness of the histological features of idelalisib-associated colitis is important to distinguish it from potential mimickers such as GVHD and infectious colitis.
idelalisib是磷脂酰肌醇3激酶δ亚型的选择性抑制剂,于2014年被美国食品药品监督管理局批准用于治疗复发的慢性淋巴细胞白血病和惰性非霍奇金淋巴瘤。药物性胃肠道损伤是一种相对常见但通常未被充分认识的疾病实体。
我们报告了一例56岁男性,有复发滤泡性淋巴瘤病史,接受异基因骨髓移植后,在开始使用idelalisib 6个月后出现严重腹泻,并伴有类似移植物抗宿主病(GVHD)的皮疹。他接受了结肠镜检查,显示结肠和回肠末端外观大致正常。检查过程中采集的活检显示轻度活动性回肠炎、结肠炎和直肠炎,伴有频繁的上皮细胞凋亡和局灶性上皮内淋巴细胞增多。皮肤活检显示亚急性海绵状皮炎,提示接触性皮炎或湿疹样药物反应。鉴于停药后症状缓解以及皮肤和结肠活检结果,症状归因于idelalisib。
高度的临床怀疑以及对idelalisib相关性结肠炎组织学特征的认识,对于将其与潜在的类似疾病如GVHD和感染性结肠炎区分开来很重要。