Department of Pathology and Molecular Medicine, 2nd Faculty of Medicine, Charles University and Motol University Hospital, V Uvalu 84, 150 06, Prague 5, Czech Republic.
Department of Paediatrics, 2nd Faculty of Medicine, Charles University and Motol University Hospital, V Uvalu 84, 150 06, Prague 5, Czech Republic.
Dig Dis Sci. 2018 Jul;63(7):1811-1818. doi: 10.1007/s10620-018-5018-3. Epub 2018 Mar 14.
Diagnosis of pediatric inflammatory bowel diseases (IBD) remains challenging. We aimed at the value of immunohistochemical assessment of CD30+ lymphocytes in the intestinal mucosa in differential diagnosis between pediatric Crohn's disease (CD) and ulcerative colitis (UC) and its utility as a predictor of future differentiation in patients with IBD unclassified (IBDU).
Seventy-four treatment naive pediatric patients with IBD (33 CD, 30 UC and 11 IBDU) were enrolled into the study. Biopsy samples from six different regions (terminal ileum, cecum, ascending colon, transverse colon, descending colon and rectum) were immunohistochemically stained with anti-CD30 antibody, and the number of positive cells per one high power field was quantified.
Significant differences between CD and UC were found when compared total counts of CD30+ cells in median numbers, mean values and maximal numbers and also for separate counts in terminal ileum, transverse colon, descending colon and rectum. The most profound difference between CD and UC was shown for total median values of CD30+ cells and for the values in rectal localization. The difference was independent on the intensity of inflammation. A cutoff value of 2.5 CD30+ cells with sensitivity 83% and specificity 90% was found for the rectum. There was no difference between patients with CD and IBDU, but a marked difference between UC and IBDU patients was revealed.
Histopathological assessment of biopsy with rectal CD30+ count is reliable and simple method that could help in differential diagnosis among IBD subtypes in children with IBD.
儿科炎症性肠病(IBD)的诊断仍然具有挑战性。我们旨在评估肠黏膜中 CD30+淋巴细胞的免疫组织化学评估在儿童克罗恩病(CD)和溃疡性结肠炎(UC)之间的鉴别诊断中的价值,及其作为未分类 IBD(IBDU)患者未来分化的预测因子的效用。
本研究纳入了 74 名未经治疗的儿科 IBD 患者(33 例 CD、30 例 UC 和 11 例 IBDU)。对来自 6 个不同部位(末端回肠、盲肠、升结肠、横结肠、降结肠和直肠)的活检样本进行抗 CD30 抗体免疫组织化学染色,并对每高倍视野的阳性细胞数进行定量。
在 CD 和 UC 之间比较了 CD30+细胞的总计数中位数、平均值和最大值,以及末端回肠、横结肠、降结肠和直肠的单独计数时,发现了显著差异。CD 和 UC 之间最显著的差异是 CD30+细胞的总中位数和直肠定位的数值。这种差异与炎症的强度无关。在直肠中,发现 CD30+细胞的截断值为 2.5,其敏感性为 83%,特异性为 90%。在 CD 和 IBDU 患者之间没有差异,但在 UC 和 IBDU 患者之间显示出明显差异。
对具有直肠 CD30+计数的活检进行组织病理学评估是一种可靠且简单的方法,可以帮助儿童 IBD 患者鉴别 IBD 亚型。