Kato Hiroyuki, Naganuma Tatsushi, Iizawa Yusuke, Kitagawa Masato, Tanaka Minoru, Isaji Shuji
Department of Surgery, Saiseikai Matsusaka General Hospital, Mie, Japan.
J Hepatobiliary Pancreat Surg. 2008;15(6):659-63. doi: 10.1007/s00534-007-1283-9. Epub 2008 Nov 7.
Primary lymphoma of the gallbladder is an exceedingly rare disease. We experienced an asymptomatic case of primary non-Hodgkin's lymphoma of the gallbladder in a 55-year-old woman in whom laparoscopic cholecystectomy made a definite diagnosis. Abdominal computed tomography revealed a 4-cm gallbladder tumor with markedly enlarged lymph nodes in the retropancreatic area. Despite the marked involvement of lymph nodes, serum levels of carcinoembryonic antigen (CEA) and carbohydrate antigen (CA) 19-9 were not elevated. The discrepancy between the imaging findings and the patient's mild clinical presentation led us to suspect that the tumor was a lymphoma. We examined serum markers of lymphoma, revealing slight elevations of interleukin (IL)-2 receptor and thymidine kinase. Laparoscopic cholecystectomy for a total biopsy was performed successfully, and the results of intraoperative frozen-section examination led us to have a high suspicion of malignant lymphoma. The final diagnosis was large diffuse B-cell lymphoma of the gallbladder with a positive CD20 antibody reaction. The patient received postoperative chemotherapy with R-CHOP (rituximab, 500 mg; cyclophosphamide, 1000 mg; adriamycin, 68 mg; vincristine, 1.9 mg; and prednisone, 80 mg) starting on postoperative day 12. She achieved complete remission and is still in complete remission 3 years and 2 months after the cholecystectomy. In conclusion, gallbladder lymphoma should be added to the differential diagnosis of gallbladder tumors, especially when the imaging findings and clinical presentation are not consistent with typical signs of gallbladder carcinoma, and laparoscopic cholecystectomy is helpful for the confirmation of suspicious cases.
原发性胆囊淋巴瘤是一种极为罕见的疾病。我们遇到一例55岁女性原发性非霍奇金胆囊淋巴瘤的无症状病例,通过腹腔镜胆囊切除术得以明确诊断。腹部计算机断层扫描显示一个4厘米的胆囊肿瘤,胰后区域淋巴结明显肿大。尽管淋巴结有明显受累,但癌胚抗原(CEA)和糖类抗原(CA)19-9的血清水平并未升高。影像学检查结果与患者轻微的临床表现之间的差异使我们怀疑该肿瘤是淋巴瘤。我们检测了淋巴瘤的血清标志物,发现白细胞介素(IL)-2受体和胸苷激酶略有升高。成功进行了腹腔镜胆囊切除术以获取完整活检,术中冰冻切片检查结果使我们高度怀疑为恶性淋巴瘤。最终诊断为胆囊大弥漫性B细胞淋巴瘤,CD20抗体反应呈阳性。患者在术后第12天开始接受R-CHOP(利妥昔单抗,500毫克;环磷酰胺,1000毫克;阿霉素,68毫克;长春新碱,1.9毫克;泼尼松,80毫克)术后化疗。她实现了完全缓解,在胆囊切除术后3年零2个月仍处于完全缓解状态。总之,胆囊淋巴瘤应纳入胆囊肿瘤的鉴别诊断,尤其是当影像学检查结果和临床表现与典型胆囊癌体征不一致时,腹腔镜胆囊切除术有助于确诊可疑病例。