Dundas S A, Dutton J, Skipworth P
Department of Pathology, Southport & Formby NHS Trust, District General Hospital, UK.
Histopathology. 1997 Jul;31(1):60-6. doi: 10.1046/j.1365-2559.1997.5810818.x.
In order to assess the validity of previously proposed criteria for the differentiation of chronic inflammatory bowel disease (CIBD) from acute self-limiting colitis (ASLC) all rectal biopsies were reported by a single histopathologist with a long-term gastrointestinal interest over a 4.5-year period.
The presence or absence of distorted crypt architecture, increased lymphocytes and plasma cells, villous mucosal architecture, granulomata, basal lymphoid aggregates, basal giant cells and Paneth cell metaplasia was noted for each biopsy. The definite presence of any of the above features, with the exception of intramucosal granulomata, was regarded as indicative of CIBD. Eighteen months later all available case notes were examined and the presenting clinical symptoms and working clinical diagnosis extracted. The final diagnosis, histopathological diagnosis and the presence or absence of any of the above histopathological features were correlated and the positive predictive value of each histopathological feature was calculated. A correct diagnosis of either CIBD or ASLC was made in 80 of 84 and 29 of 31 cases, respectively.
Villous mucosal architecture and Paneth cell metaplasia were found to be specific features of CIBD. Distorted crypt architecture, basal lymphoid aggregates and plasma cell infiltration of the lamina propria were also useful features but strict definition of these features is required and discussed. Intramucosal epithelioid granulomas were identified in eight cases of CIBD and four cases of ASLC. In association with ruptured crypts intramucosal granulomas are not specific features of Crohn's colitis.
为评估先前提出的区分慢性炎症性肠病(CIBD)和急性自限性结肠炎(ASLC)标准的有效性,由一位长期关注胃肠病学的病理学家对4.5年期间的所有直肠活检报告进行分析。
记录每次活检中隐窝结构扭曲、淋巴细胞和浆细胞增多、绒毛状黏膜结构、肉芽肿、基底淋巴聚集、基底巨细胞和潘氏细胞化生的有无。除黏膜内肉芽肿外,上述任何特征的明确存在被视为CIBD的指征。18个月后,检查所有可用的病例记录,提取呈现的临床症状和工作临床诊断。将最终诊断、组织病理学诊断与上述任何组织病理学特征的有无进行关联,并计算每个组织病理学特征的阳性预测值。分别在84例中的80例和31例中的29例中正确诊断为CIBD或ASLC。
绒毛状黏膜结构和潘氏细胞化生被发现是CIBD的特异性特征。隐窝结构扭曲、基底淋巴聚集和固有层浆细胞浸润也是有用的特征,但需要对这些特征进行严格定义并加以讨论。在8例CIBD和4例ASLC中发现了黏膜内上皮样肉芽肿。与隐窝破裂相关的黏膜内肉芽肿不是克罗恩病性结肠炎的特异性特征。