Xiang Zhang, Onoda Naoyoshi, Ohira Masaichi, Yukawa Tomomi, Uchida Toshiyuki, Arakawa Tetsuo, Wakasa Kenichi, Chung Kosei Hirakawa-Yong Suk
Department of Surgical Oncology, Institute of Geriatrics and Medical Science, Osaka City University Graduate School of Medicine, Osaka, Japan.
Hepatogastroenterology. 2004 May-Jun;51(57):732-5.
We present a case of mucosa-associated lymphoid tissue (MALT) lymphoma of the duodenum treated with surgical resection. A 64-year-old woman underwent upper gastrointestinal endoscopy because of melena. Examinations revealed an ulcer-forming lesion at the second portion of the duodenum that was diagnosed histologically as low-grade MALT lymphoma. We attempted Helicobacter pylori eradication therapy, although all the tests revealed negative results for its infection. No sign of remission was observed and we performed surgical resection. The patient has shown no sign of recurrence at present, 39 months after the operation. Duodenal MALT lymphoma is a rare entity. Only 17 cases have been reported in the English literature. We summarized the characteristics of the disease and tried to figure out differences in comparison with those in the stomach, including the involvement of the Helicobacter pylori infection.
我们报告一例经手术切除治疗的十二指肠黏膜相关淋巴组织(MALT)淋巴瘤。一名64岁女性因黑便接受了上消化道内镜检查。检查发现十二指肠第二部有一个溃疡形成性病变,组织学诊断为低度MALT淋巴瘤。尽管所有检测均显示幽门螺杆菌感染呈阴性结果,但我们仍尝试进行幽门螺杆菌根除治疗。未观察到缓解迹象,于是我们进行了手术切除。术后39个月,该患者目前未显示复发迹象。十二指肠MALT淋巴瘤是一种罕见的疾病。英文文献中仅报道了17例。我们总结了该疾病的特征,并试图找出与胃部疾病特征的差异,包括幽门螺杆菌感染的情况。