Ahn M J, Park Y W, Han D, Choi J H, Shin S J, Yoon B C, Choi H S, Lee Y Y, Jung T J, Choi I Y, Park M H, Kim I S
Department of Internal Medicine, Department of Pathology, Hanyang University College of Medicine, Seoul, Korea.
Korean J Intern Med. 2000 Dec;15(3):245-9. doi: 10.3904/kjim.2000.15.3.245.
Primary intestinal T-cell lymphoma is a rare disease entity, which is approximately 10% to 25% of intestinal lymphomas, and most of the lymphomas occur in the small intestine. We report here a case of a 56-year-old woman who has been suffering from chronic diarrhea and weight loss for 6 months. Abdominal CT scan and small bowel series showed diffuse wall thickening of the small bowel. Gastroscopic examination showed diffuse erythematous lesions on the esophagus and small gastric ulcerations on the antrum of the stomach, and colonoscopic examination also showed multiple punched-out ulcerations and erosions on the entire colon, including the sigmoid colon to the terminal ileum. Diffuse infiltration of CD 3 positive lymphoma cells was found on biopsy. The patient was diagnosed as primary intestinal T-cell lymphoma with diffuse involvement of the entire gastrointestinal tracts from the esophagus to the rectum. Although the patient received systemic combination chemotherapy and achieved partial response initially, the lymphoma relapsed repeatedly.
原发性肠道T细胞淋巴瘤是一种罕见的疾病实体,约占肠道淋巴瘤的10%至25%,且大多数淋巴瘤发生在小肠。我们在此报告一例56岁女性患者,她出现慢性腹泻和体重减轻6个月。腹部CT扫描和小肠造影显示小肠壁弥漫性增厚。胃镜检查显示食管有弥漫性红斑病变,胃窦有小溃疡,结肠镜检查还显示整个结肠包括乙状结肠至回肠末端有多个圆形溃疡和糜烂。活检发现CD 3阳性淋巴瘤细胞弥漫浸润。该患者被诊断为原发性肠道T细胞淋巴瘤,累及从食管到直肠的整个胃肠道。尽管患者接受了全身联合化疗,最初取得了部分缓解,但淋巴瘤反复复发。