Armes J, Gee D C, Macrae F A, Schroeder W, Bhathal P S
Department of Anatomical Pathology, Royal Melbourne Hospital, Parkville, Victoria, Australia.
J Clin Pathol. 1992 Sep;45(9):784-7. doi: 10.1136/jcp.45.9.784.
To determine: (1) whether there is an association between collagenous colitis and coeliac disease or lymphocytic colitis; (2) the distribution of lymphocyte subsets and macrophages in the lamina propria and surface epithelial layer in collagenous colitis; and (3) the colorectal distribution of the disease and whether a mucosal biopsy specimen, using a flexible sigmoidoscope, is sufficient to diagnose it.
The clinical data and colorectal biopsy specimens from 38 patients with collagenous colitis were studied. In 10, small bowel biopsy specimens were also available for review. Immunostaining of the mucosal lymphoid infiltrate with a panel of relevant antibodies was carried out on formalin fixed tissue in seven cases; in three the phenotyping was performed on fresh biopsy specimens separately frozen or fixed in B5 solution.
Coeliac disease was found in four out of the 10 patients with collagenous colitis who had had a small bowel biopsy, in contrast to the prevalence of the disease in Australia of 1 in 3000. Collagenous colitis did not respond to gluten withdrawal. Five of 29 (17%) of the patients had a mixed pattern of lymphocytic and collagenous colitis. Immunostaining of the lymphoid infiltrate showed that the striking increase in intraepithelial lymphocytes in collagenous colitis was due to an influx of CD8 positive cells. The occurrence and severity of collagenous colitis along the large bowel were independent of the anatomical site, and in more than 90% of cases biopsy specimens from the sigmoid colon or rectum were diagnostic.
There is a very high incidence of coeliac disease among patients with collagenous colitis so that jejunal biopsy should be an essential part of their investigations, especially if symptoms persist. However, only a minority showed a mixed pattern of lymphocytic and collagenous colitis. The intraepithelial lymphocytes in collagenous colitis are CD8 positive cells. Collagenous colitis can be diagnosed from rectal or sigmoid colon biopsy specimens in more than 90% of cases.
确定:(1)胶原性结肠炎与乳糜泻或淋巴细胞性结肠炎之间是否存在关联;(2)胶原性结肠炎固有层和表面上皮层中淋巴细胞亚群和巨噬细胞的分布;(3)该疾病在结直肠的分布情况,以及使用乙状结肠镜获取的黏膜活检标本是否足以诊断该病。
研究了38例胶原性结肠炎患者的临床资料和结直肠活检标本。其中10例患者还提供了小肠活检标本以供复查。对7例福尔马林固定组织的黏膜淋巴浸润进行了一组相关抗体的免疫染色;3例对分别冷冻或固定于B5溶液的新鲜活检标本进行了表型分析。
在10例接受小肠活检的胶原性结肠炎患者中,有4例发现患有乳糜泻,而澳大利亚该病的患病率为1/3000。胶原性结肠炎对去除麸质无反应。29例患者中有5例(17%)表现为淋巴细胞性和胶原性结肠炎的混合模式。对淋巴浸润的免疫染色显示,胶原性结肠炎中上皮内淋巴细胞的显著增加是由于CD8阳性细胞的流入。胶原性结肠炎在大肠的发生和严重程度与解剖部位无关,在超过90%的病例中,乙状结肠或直肠的活检标本具有诊断价值。
胶原性结肠炎患者中乳糜泻的发病率非常高,因此空肠活检应作为其检查的重要组成部分,尤其是症状持续时。然而,只有少数患者表现为淋巴细胞性和胶原性结肠炎的混合模式。胶原性结肠炎中的上皮内淋巴细胞是CD8阳性细胞。超过90%的病例可通过直肠或乙状结肠活检标本诊断胶原性结肠炎。