Department of Internal Medicine, Toyama Prefectural Central Hospital, Nishinagae 2-2-78, Toyama, 930-0975, Japan.
Department of Pathology, Toyama Prefectural Central Hospital, Toyama, Japan.
Clin J Gastroenterol. 2022 Dec;15(6):1145-1150. doi: 10.1007/s12328-022-01692-8. Epub 2022 Sep 2.
Extranodal marginal zone lymphoma of mucosa-associated lymphoid tissue (MALT lymphoma) extremely rarely arise in extrahepatic biliary tract. Here, we report a case of bile duct MALT lymphoma diagnosed with direct cholangioscopy. The patient was an 80-year-old female with history of esophageal cancer, and had been occasionally treated with balloon dilatation for anastomotic stricture. She was referred to our hospital for treatment of choledocholithiasis. Since transesophageal endoscope insertion was impossible, stone extraction by transjejunal approach was performed. When gastroduodenoscope was directly inserted to the bile duct (direct cholangioscopy), accidentally two flat lesions with development of large atypical vessels in hilar region were noted. Biopsy revealed diffuse infiltration of CD20 positive small- to medium-sized atypical lymphocytes. A diagnosis of bile duct MALT lymphoma was made. The patient underwent eight courses of chemotherapy with rituximab alone, with no evident complications. Although biliary tract MALT lymphoma is rare, advances in cholangioscopy may promote encounter with such lesions. Accumulation of endoscopic figures of biliary tract MALT lymphoma is required.
黏膜相关淋巴组织(MALT)结外边缘区淋巴瘤极少见发生于肝外胆管。在此,我们报告一例经直接胆管镜诊断的胆管 MALT 淋巴瘤。患者为 80 岁女性,有食管癌病史,曾间断行球囊扩张术治疗吻合口狭窄。因胆石症就诊于我院,因无法行经食管内镜插入,遂行经空肠途径取石。当胃十二指肠镜直接插入胆管(直接胆管镜)时,偶然发现肝门区有两个平坦的病变,伴有大的不典型血管发育。活检显示弥漫性浸润 CD20 阳性的中小异型淋巴细胞。诊断为胆管 MALT 淋巴瘤。患者接受了单独利妥昔单抗 8 个疗程的化疗,无明显并发症。虽然胆管 MALT 淋巴瘤罕见,但胆管镜技术的进步可能会促进对这类病变的发现。需要积累胆管 MALT 淋巴瘤的内镜图像。