Jiao Guohui, Zheng Zhongqing, Jiang Kui, Zhang Jie, Wang Bangmao
Department of Gastroenterology, Tianjin Medical University General Hospital, Tianjin 300052, P.R. China.
Oncol Lett. 2014 Jul;8(1):91-94. doi: 10.3892/ol.2014.2105. Epub 2014 Apr 29.
The gastrointestinal tract is the most common location for primary extranodal non-Hodgkin lymphoma (NHL) with cases less commonly found in the intestine. The majority of primary intestinal B-cell lymphomas are exophytic, whereas enteropathy-associated T-cell lymphomas present predominantly as thickened plaques, ulcers or strictures. Crohn's disease (CD) is a chronic inflammatory disease of the intestines with fissures and ulcers, which is difficult for clinicians to diagnose based on endoscopic observations alone. Malignant lymphoma must be considered when clinically diagnosed CD is refractory to medication or when its clinical course becomes aggressive. The current study presents a rare case of primary colon T-cell lymphoma in a 16-year-old male with poor prognosis, as well as a case of gastrointestinal lymphoma occurring in the duodenum and colon in a 62-year-old male with a 10-year history of NHL. It was difficult to determine the diagnosis by a single endoscopic biopsy as the majority of biopsy specimens revealed mixed inflammation within which the lymphoma cells were difficult to identify. The present study indicated that it is important to recognize ulcerative or stenotic lymphoma and to differentiate it from CD as it exhibits a much more aggressive clinical behavior. The correct diagnosis may be confirmed by careful histopathological study and ancillary examination.
胃肠道是原发性结外非霍奇金淋巴瘤(NHL)最常见的发病部位,肠道内较少见。大多数原发性肠道B细胞淋巴瘤为外生性,而肠病相关T细胞淋巴瘤主要表现为增厚的斑块、溃疡或狭窄。克罗恩病(CD)是一种伴有裂隙和溃疡的肠道慢性炎症性疾病,临床医生仅通过内镜观察很难做出诊断。当临床诊断的CD对药物治疗无效或临床病程进展迅速时,必须考虑恶性淋巴瘤的可能。本研究报告了1例预后不良的16岁男性原发性结肠T细胞淋巴瘤罕见病例,以及1例有10年NHL病史的62岁男性十二指肠和结肠发生胃肠道淋巴瘤的病例。由于大多数活检标本显示为混合性炎症,其中淋巴瘤细胞难以识别,因此通过单次内镜活检很难确定诊断。本研究表明,认识溃疡性或狭窄性淋巴瘤并将其与CD区分开来很重要,因为它表现出更具侵袭性的临床行为。通过仔细的组织病理学研究和辅助检查可确诊。