1 Department of Pathology, Zhongnan Hospital of Wuhan University, Wuhan, P.R. China.
2 Department of Pathology, The University of Chicago, Chicago, IL, USA.
Int J Immunopathol Pharmacol. 2019 Jan-Dec;33:2058738419829387. doi: 10.1177/2058738419829387.
There is a significant overlap between intestinal lymphoproliferative disorders (LPDs) and inflammatory conditions of the intestine, including inflammatory bowel disease (IBD), in clinical, endoscopic, or histologic appearance, leading to diagnostic challenges. We report two cases of monomorphic epitheliotropic intestinal T-cell lymphoma (MEITL) that were initially considered to be ulcerative colitis (UC) and lymphocytic colitis, respectively. Both patients presented with diarrhea and abdominal pain. Colonoscopy revealed hyperemia and scattered shallow ulcerations in the colon, without obvious mass. Microscopically, the first case exhibited features of active chronic colitis. The second case exhibited features mimicking lymphocytic colitis and ileitis. Correct diagnosis of lymphoma was established when the cases were received as consultation, with additional ancillary tests performed. Being familiar with the endoscopic features and unusual histologic patterns of MEITL described here is critical for prompt diagnosis and timely treatment, which may be conductive to a better prognosis.
肠淋巴组织增生性疾病(LPD)与肠道炎症性疾病(包括炎症性肠病,IBD)在临床表现、内镜表现或组织学表现上有很大的重叠,导致诊断困难。我们报告了两例最初被认为分别是溃疡性结肠炎(UC)和淋巴细胞性结肠炎的单形上皮亲嗜性肠 T 细胞淋巴瘤(MEITL)。两例患者均表现为腹泻和腹痛。结肠镜检查显示结肠充血,散在浅溃疡,无明显肿块。显微镜下,第一个病例表现为活动性慢性结肠炎的特征。第二个病例表现为类似于淋巴细胞性结肠炎和回肠炎的特征。当这些病例被作为会诊收到时,通过辅助检查,最终做出了淋巴瘤的正确诊断。熟悉 MEITL 的内镜特征和不常见的组织学模式对于及时诊断和治疗至关重要,这可能有助于改善预后。