Fine K D, Lee E L, Meyer R L
Department of Pathology, Baylor University Medical Center, Dallas, TX 75246, USA.
Hum Pathol. 1998 Dec;29(12):1433-40. doi: 10.1016/s0046-8177(98)90012-0.
Colonic histopathology in some patients with untreated celiac sprue and refractory sprue has been said to be indistinguishable from lymphocytic colitis, but there have been no objective comparisons on which this is based. The purpose of this study was to determine the prevalence and to characterize the nature of colonic histopathology at the time of diagnosis in patients with celiac or refractory sprue. Colonoscopic biopsy specimens obtained at the time of diagnosis from 16 patients with celiac sprue, six patients with refractory sprue, nine patients with lymphocytic colitis, and five normal controls were analyzed blindly by histological and morphometric methods, quantitating the number and specific subtypes of inflammatory cells within the lamina propria and epithelium. Immunoperoxidase staining of intraepithelial lymphocytes with a monoclonal antibody to CD8 also was performed. Three of 16 patients with untreated celiac sprue (19%) were thought to have colonic histological abnormalities, which by morphometry consisted of slightly increased numbers of lymphocytes in the surface epithelium and lamina propria, many of which were CD8-positive. These abnormalities were distinguishable from lymphocytic colitis by the lack of increased overall lamina propria cellularity and surface epithelial abnormalities, and by fewer intraepithelial lymphocytes. In refractory sprue, colonic histological abnormalities were more frequent than in celiac sprue, occurring in four of six patients (67%), more pronounced, and identical to those in the lymphocytic colitis syndrome. However, colonic intraepithelial lymphocytes in lymphocytic colitis were mostly CD8-positive, whereas those in the colitis of refractory sprue rarely were. Mild colonic lymphocytosis in patients with untreated celiac sprue should be distinguished from lymphocytic colitis by the lack of surface epithelial abnormalities, the lack of increased cellularity of the lamina propria, and the lack of ongoing watery diarrhea after treatment with a gluten-free diet. In contrast, colonic histopathology in refractory sprue is indistinguishable from lymphocytic colitis, although immunohistochemical differences do exist.
据说,一些未经治疗的乳糜泻和难治性口炎性腹泻患者的结肠组织病理学表现与淋巴细胞性结肠炎难以区分,但尚无基于此的客观比较。本研究的目的是确定乳糜泻或难治性口炎性腹泻患者诊断时结肠组织病理学的患病率并描述其特征。对诊断时从16例乳糜泻患者、6例难治性口炎性腹泻患者、9例淋巴细胞性结肠炎患者和5例正常对照者获取的结肠镜活检标本进行组织学和形态计量学方法的盲法分析,对固有层和上皮内炎性细胞的数量和特定亚型进行定量。还用抗CD8单克隆抗体对上皮内淋巴细胞进行免疫过氧化物酶染色。16例未经治疗的乳糜泻患者中有3例(19%)被认为存在结肠组织学异常,通过形态计量学分析,这些异常表现为表面上皮和固有层中淋巴细胞数量略有增加,其中许多为CD8阳性。这些异常与淋巴细胞性结肠炎的区别在于固有层总体细胞增多不明显、表面上皮无异常,且上皮内淋巴细胞较少。在难治性口炎性腹泻中,结肠组织学异常比乳糜泻更常见,6例患者中有4例(67%)出现,且更明显,与淋巴细胞性结肠炎综合征中的表现相同。然而,淋巴细胞性结肠炎中的结肠上皮内淋巴细胞大多为CD8阳性,而难治性口炎性腹泻结肠炎中的则很少是。未经治疗的乳糜泻患者的轻度结肠淋巴细胞增多症应与淋巴细胞性结肠炎相区分,其依据是缺乏表面上皮异常、固有层细胞增多不明显,以及无麸质饮食治疗后持续的水样腹泻。相比之下,难治性口炎性腹泻的结肠组织病理学与淋巴细胞性结肠炎难以区分,尽管存在免疫组化差异。