Swan N C, Geoghegan J G, O'Donoghue D P, Hyland J M, Sheahan K
Department of Pathology, St. Vincent's Hospital, Dublin, Ireland.
Dis Colon Rectum. 1998 Dec;41(12):1511-5. doi: 10.1007/BF02237298.
The morphologic features of fulminant colitis may be nonspecific, making differentiation between ulcerative colitis and Crohn's disease difficult, even after colectomy. The aims of this study were 1) to identify histologic features that accurately differentiated ulcerative colitis, Crohn's disease, and indeterminate colitis in fulminant colectomy specimens; 2) to determine how frequently subsequent clinical course altered the pathologic diagnosis; and 3) to evaluate the natural history of histologically diagnosed indeterminate colitis.
Ninety-five fulminant colectomy specimens were evaluated, of which 85 had an original diagnosis of fulminant inflammatory bowel disease. Complete pathologic material and comprehensive clinical follow-up information was available on 67 cases of inflammatory bowel disease. These were re-evaluated in a blinded fashion, and histopathologic features were compared with the original diagnosis and reviewed in the light of subsequent clinical behavior to reach a final diagnosis.
Evaluation of macroscopic features was not helpful in differentiating ulcerative colitis from Crohn's disease. Microscopic examination correctly diagnosed ulcerative colitis or Crohn's disease in only 58 of 67 (87 percent) cases. A further three cases (4 percent) were definitively classified after correlation with clinical data, leaving a residual six cases that were diagnosed as indeterminate colitis. Granulomas and lymphoid aggregates were the two most specific indicators of Crohn's disease.
Histopathologic evaluation alone has limitations in the accurate classification of fulminant inflammatory bowel disease. Histologically diagnosed indeterminate colitis is a heterogeneous group that may include some patients who subsequently prove to have ulcerative colitis or Crohn's disease.
暴发性结肠炎的形态学特征可能不具有特异性,即使在结肠切除术后,也难以区分溃疡性结肠炎和克罗恩病。本研究的目的是:1)在暴发性结肠切除标本中识别能够准确区分溃疡性结肠炎、克罗恩病和不确定性结肠炎的组织学特征;2)确定后续临床病程改变病理诊断的频率;3)评估经组织学诊断的不确定性结肠炎的自然病程。
对95例暴发性结肠切除标本进行评估,其中85例最初诊断为暴发性炎症性肠病。67例炎症性肠病患者有完整的病理资料和全面的临床随访信息。对这些病例进行盲法重新评估,将组织病理学特征与最初诊断进行比较,并根据后续临床行为进行复查以得出最终诊断。
宏观特征评估对区分溃疡性结肠炎和克罗恩病并无帮助。显微镜检查仅在67例病例中的58例(87%)中正确诊断出溃疡性结肠炎或克罗恩病。另外3例(4%)经与临床资料相关分析后得到明确分类,剩下6例被诊断为不确定性结肠炎。肉芽肿和淋巴样聚集是克罗恩病的两个最具特异性的指标。
仅组织病理学评估在暴发性炎症性肠病的准确分类方面存在局限性。经组织学诊断的不确定性结肠炎是一个异质性群体,可能包括一些随后被证明患有溃疡性结肠炎或克罗恩病的患者。