McCabe Patrick, Alli-Akintade Latifat, Stondell Jesse
Department of Internal Medicine, University of California Davis Medical Center, Sacramento, CA.
Division of Gastroenterology and Hepatology, University of California Davis Medical Center, Sacramento, CA.
ACG Case Rep J. 2017 Feb 1;4:e19. doi: 10.14309/crj.2017.19. eCollection 2017.
Autoimmune enteropathy (AIE) is rare but damaging. The lack of consistent objective findings makes diagnosis a challenge. A 45-year-old male developed noninfectious diarrhea with significant weight loss and electrolyte abnormalities. Computed tomography delineated enteritis. Colonoscopy and esophagogastroduodenoscopy showed villous atrophy, chronic inflammation, and ulceration of the terminal ileum and cecum. Pathology showed cryptitis with apoptosis and abscesses throughout the small and large bowel and absent goblet cells. Steroids rapidly improved symptoms. Anti-enterocyte antibody serologies were negative. Management can be challenging, and, in this case, the patient initially improved with budesonide and infliximab but required alternative anti-tumor necrosis factor therapy after relapsing. This is an unusual presentation of seronegative AIE, which should be considered in cases of persistent severe diarrhea.
自身免疫性肠病(AIE)虽罕见但具有破坏性。由于缺乏一致的客观检查结果,诊断颇具挑战。一名45岁男性出现非感染性腹泻,伴有显著体重减轻和电解质异常。计算机断层扫描显示有肠炎。结肠镜检查及食管胃十二指肠镜检查显示绒毛萎缩、慢性炎症以及回肠末端和盲肠溃疡。病理检查显示全小肠和大肠存在隐窝炎伴凋亡及脓肿,且杯状细胞缺失。类固醇药物迅速改善了症状。抗肠细胞抗体血清学检查结果为阴性。治疗可能具有挑战性,在本病例中,患者最初使用布地奈德和英夫利昔单抗后病情改善,但复发后需要改用其他抗肿瘤坏死因子疗法。这是血清阴性AIE的一种不寻常表现,对于持续性严重腹泻病例应予以考虑。