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表现为梗阻性黄疸的胆总管原发性非霍奇金淋巴瘤。

Primary non-Hodgkin's lymphoma of the common bile duct presenting as obstructive jaundice.

作者信息

Joo Young-Eun, Park Chang-Hwan, Lee Wan-Sik, Kim Hyun-Soo, Choi Sung-Kyu, Cho Chol-Kyoon, Rew Jong-Sun, Kim Sei-Jong, Maetani Iruru

机构信息

Department of Internal Medicine, Chonnam National University Medical School, 8 Hak-Dong, Dong-ku, Gwangju 501-757, Korea.

出版信息

J Gastroenterol. 2004 Jul;39(7):692-6. doi: 10.1007/s00535-004-1367-0.

Abstract

Primary non-Hodgkin's lymphoma of the extrahepatic bile duct presenting as obstructive jaundice is an extremely rare disease. At this writing, a review of the medical literature disclosed 17 reported cases of primary non-Hodgkin's lymphoma arising from the extrahepatic bile duct. We, herein, report an additional case of obstructive jaundice caused by primary non-Hodgkin's lymphoma of the common bile duct, in a 21-year-old woman. Our patient showed clinical evidence of obstructive jaundice, and endoscopic retrograde cholangiopancreatography and abdominal magnetic resonance imaging demonstrated a long strictured segment of the common bile duct with proximal bile duct dilatation. These clinical and radiological findings resembled those of cholangiocarcinoma. Resection of the common bile duct tumor, cholecystectomy, lymph node dissection, and Roux-en-Y hepaticojejunostomy were carried out. Histology and immunohistochemistry of the resected specimen confirmed a diffuse large B-cell-type malignant lymphoma involving the common bile duct. She received four courses of combination chemotherapy, including cyclophosphamide, doxorubicin, vincristine, and prednisone (CHOP), and 3060 cGy external irradiation. She has been well, without evidence of tumor recurrence, 17 months after the surgery. In summary, first, primary non-Hodgkin's lymphoma of the extrahepatic bile duct, despite its rarity, should be considered in the differential diagnosis of causes of obstructive jaundice. Second, an accurate histopathologic diagnosis and surgical resection, if feasible, combined with chemotherapy with or without radiotherapy may be the approach to offer a chance for cure.

摘要

表现为梗阻性黄疸的肝外胆管原发性非霍奇金淋巴瘤是一种极其罕见的疾病。撰写本文时,查阅医学文献发现有17例关于肝外胆管原发性非霍奇金淋巴瘤的报道病例。在此,我们报告一例21岁女性因胆总管原发性非霍奇金淋巴瘤导致梗阻性黄疸的病例。我们的患者有梗阻性黄疸的临床证据,内镜逆行胰胆管造影和腹部磁共振成像显示胆总管有一长段狭窄,近端胆管扩张。这些临床和影像学表现与胆管癌相似。进行了胆总管肿瘤切除、胆囊切除、淋巴结清扫以及Roux-en-Y肝空肠吻合术。切除标本的组织学和免疫组化证实为累及胆总管的弥漫性大B细胞型恶性淋巴瘤。她接受了四个疗程的联合化疗,包括环磷酰胺、阿霉素、长春新碱和泼尼松(CHOP方案),并接受了3060 cGy的外照射。术后17个月,她情况良好,无肿瘤复发迹象。总之,第一,肝外胆管原发性非霍奇金淋巴瘤尽管罕见,但在梗阻性黄疸病因的鉴别诊断中应予以考虑。第二,准确的组织病理学诊断和可行的手术切除,联合化疗或放疗,可能是提供治愈机会的治疗方法。

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