Fujita Akashi, Tajika Masahiro, Tanaka Tsutomu, Ishihara Makoto, Hirayama Yutaka, Mizuno Nobumasa, Hara Kazuo, Hijioka Susumu, Imaoka Hiroshi, Yoshida Tsukasa, Okuno Nozomi, Hieda Nobuhiro, Hirayama Takashi, Shibuya Hitoshi, Kondo Hisashi, Suzuki Hirotaka, Toriyama Kazuhiro, Yatabe Yasushi, Yamao Kenji, Niwa Yasumasa
Departments of Gastroenterology, Aichi Cancer Center Hospital.
Departments of Endoscopy, Aichi Cancer Center Hospital.
Nagoya J Med Sci. 2017 Feb;79(2):251-257. doi: 10.18999/nagjms.79.2.251.
translocation-positive gastric marginal zone lymphomas of mucosa-associated lymphoid tissue (MALT) lymphoma is thought to transform to diffuse large B-cell lymphoma (DLBCL) rarely. A 69-year-old man presented with epigastralgia. Esophagogastroduodenoscopy showed multiple ulcerations in the stomach. Endoscopic biopsies revealed MALT lymphoma, with infection. The patient underwent eradication therapy with no improvement, and was thereafter followed without additional therapy at his request. Twelve years after initial diagnosis, follow-up computed tomography (CT) showed multiple nodules in bilateral lungs, and a needle biopsy revealed MALT lymphoma, the same as in the stomach and translocation was found. Because he again refused additional therapy, follow-up was continued. 15 years after initial diagnosis, CT showed lymphadenopathy at the splenic hilum. At first we suspected disease progression of gastric MALT lymphoma, however a needle biopsy revealed DLBCL without . Thus, the tumor at the splenic hilum was finally diagnosed as a de novo DLBCL as a second malignancy. Although treatment with rituximab given his age and his wishes was attempted, he died of DLBCL 15 years after the initial diagnosis. We experienced an -positive gastric MALT lymphoma with concomitant DLBCL, not transformed to DLBCL over a 15-year clinical course.
伴有11;18易位的胃黏膜相关淋巴组织边缘区淋巴瘤(MALT淋巴瘤)很少转化为弥漫性大B细胞淋巴瘤(DLBCL)。一名69岁男性因上腹部疼痛就诊。食管胃十二指肠镜检查显示胃内有多处溃疡。内镜活检显示为MALT淋巴瘤,伴有幽门螺杆菌感染。患者接受根除治疗但无改善,此后应其要求未接受额外治疗进行随访。初始诊断12年后,随访计算机断层扫描(CT)显示双肺有多个结节,经针吸活检显示为MALT淋巴瘤,与胃内情况相同且发现有11;18易位。由于他再次拒绝额外治疗,继续进行随访。初始诊断15年后,CT显示脾门处有淋巴结肿大。起初我们怀疑是胃MALT淋巴瘤病情进展,然而针吸活检显示为无11;18易位的DLBCL。因此,脾门处的肿瘤最终被诊断为原发性DLBCL,为第二种恶性肿瘤。尽管考虑到他的年龄和意愿尝试使用利妥昔单抗进行治疗,但他在初始诊断15年后死于DLBCL。我们遇到了一例伴有11;18易位的胃MALT淋巴瘤合并DLBCL的病例,在15年的临床过程中未转化为DLBCL。