Mark Jacob, Fernando Shahan D, Masterson Joanne C, Pan Zhaoxing, Capocelli Kelley E, Furuta Glenn T, de Zoeten Edwin F
Section of Pediatric Gastroenterology, Hepatology, and Nutrition, Digestive Health Institute.
Pediatric Inflammatory Bowel Disease Center.
J Pediatr Gastroenterol Nutr. 2018 May;66(5):760-766. doi: 10.1097/MPG.0000000000001784.
Pediatric colonic eosinophilia represents a confounding finding with a wide differential. It is often difficult to determine which children may progress to inflammatory bowel disease (IBD), which have an eosinophilic colitis (EC), and which may have no underlying pathology. There is little guidance for the practitioner on the approach to these patients. To define the clinical presentations of colonic eosinophilia and identify factors which may aid in diagnosis we reviewed patients with colonic eosinophilia and the clinicopathologic factors associated with their diagnoses.
An 8-year retrospective chart review of children whose histopathology identified colonic eosinophilia (N = 72) compared to controls with normal biopsies (N = 35).
Patients with colonic eosinophilia had increased eosinophils/high-power field compared to controls (P < 0.001) and had 3 clinical phenotypes. Thirty-six percent had an inflammatory phenotype with elevated erythrocyte sedimentation rate (P < .0001), chronic inflammation on colonic biopsies (P < 0.001), and were diagnosed as having IBD. Thirty-seven percent were diagnosed as having EC, associated with male sex (P < 0.005) and peripheral eosinophilia (P = 0.041). Twenty-one percent had no significant colonic pathology. Forty-three percent of patients had >1 colonoscopy and 68% of these had change from initial diagnoses.
There are 3 main phenotypes of children with colonic eosinophilia. Signs of chronic systemic inflammation raise suspicion for IBD. Peripheral eosinophilia and male sex are associated with EC. A significant percent of children with colonic eosinophilia do not have colonic disease. Eosinophils/high-power field is not reliable to differentiate etiologies. Repeat colonoscopies may be required to reach final diagnoses.
小儿结肠嗜酸性粒细胞增多是一个具有广泛鉴别诊断的令人困惑的发现。通常很难确定哪些儿童可能会发展为炎症性肠病(IBD),哪些患有嗜酸性粒细胞性结肠炎(EC),以及哪些可能没有潜在病理改变。对于这些患者的处理方法,临床医生几乎没有指导意见。为了明确结肠嗜酸性粒细胞增多的临床表现并确定有助于诊断的因素,我们回顾了结肠嗜酸性粒细胞增多的患者及其诊断相关的临床病理因素。
对组织病理学确诊为结肠嗜酸性粒细胞增多的儿童(N = 72)进行了一项为期8年的回顾性病历审查,并与活检正常的对照组(N = 35)进行比较。
与对照组相比,结肠嗜酸性粒细胞增多的患者每高倍视野嗜酸性粒细胞数量增加(P < 0.001),且有3种临床表型。36%的患者具有炎症表型,红细胞沉降率升高(P < 0.0001),结肠活检有慢性炎症(P < 0.001),并被诊断为患有IBD。37%的患者被诊断为患有EC,与男性(P < 0.005)和外周嗜酸性粒细胞增多(P = 0.041)有关。21%的患者没有明显的结肠病理改变。43%的患者接受了超过1次结肠镜检查,其中68%的患者最初诊断有变化。
小儿结肠嗜酸性粒细胞增多有3种主要表型。慢性全身炎症的体征增加了IBD的怀疑。外周嗜酸性粒细胞增多和男性与EC有关。相当一部分结肠嗜酸性粒细胞增多的儿童没有结肠疾病。每高倍视野嗜酸性粒细胞数量对于鉴别病因并不可靠。可能需要重复结肠镜检查才能得出最终诊断。