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黏膜相关淋巴组织(MALT)淋巴瘤作为恶性肝门部胆管狭窄的罕见病因:一例报告并文献复习

Mucosa-associated lymphoid tissue (MALT) lymphoma as an unusual cause of malignant hilar biliary stricture: a case report with literature review.

作者信息

Park Yong Keun, Choi Jee Eun, Jung Woon Yong, Song Sung Kyu, Lee Jong In, Chung Chul-Woon

机构信息

Department of Surgery, Catholic Kwandong University International St. Mary's Hospital, Incheon, South Korea.

Catholic Kwandong University College of Medicine, Incheon, South Korea.

出版信息

World J Surg Oncol. 2016 Jun 24;14(1):167. doi: 10.1186/s12957-016-0928-z.

Abstract

BACKGROUND

Biliary strictures at the hilum of the liver arise from heterogeneous etiologies. The majority is malignant entities, but some may have benign etiologies. It is difficult to distinguish between malignant and benign biliary strictures preoperatively. It has been reported that 5~15 % of preoperative diagnoses of hilar cholangiocarcinoma turn out to be benign lesions or even other types of malignancies. Primary non-Hodgkin's lymphoma of the extrahepatic bile duct is very rare, with only a few cases reported as mucosa-associated lymphoid tissue (MALT) lymphoma arising from the hepatic duct bifurcation. We herein report a case of a female patient presenting with perihilar bile ducts obstructed by primary MALT lymphoma resembling hilar cholangiocarcinoma, along with a review of the literature.

CASE PRESENTATION

An 86-year-old female was referred to our hospital manifesting obstructive jaundice and abdominal pain. The reported imaging studies revealed distended intrahepatic bile duct with the stricture of common hepatic duct including bifurcation, which was suspicious of cholangiocarcinoma of the bile duct. The initial laboratory-confirmed cholestasis with a total bilirubin of 8.6 mg/dL, aspartate amino transferase (AST) 178 U/L, alanine transferase (ALT) 105 U/L, and the tumor marker CA 19-9 was elevated with a value of 167 U/mL. Viral markers for hepatitis B and C viruses were negative. She underwent extrahepatic bile duct resection and hepaticojejunostomy. Histological examination of the resected specimen revealed MALT lymphoma. Postoperative follow-up of 1 year has been completely uneventful, without any symptoms or disease recurrence.

CONCLUSIONS

In exceptional cases, in which radiologic and clinical features point to cholangiocarcinoma, the actual reason for obstructive jaundice and abdominal pain can be a non-Hodgkin's lymphoma. In the case of a MALT lymphoma, it can be cured with complete resection.

摘要

背景

肝门部胆管狭窄病因多样。多数为恶性病变,但部分可能为良性病因。术前难以区分恶性和良性胆管狭窄。据报道,术前诊断为肝门部胆管癌的病例中,有5%~15%最终被证明是良性病变甚至是其他类型的恶性肿瘤。肝外胆管原发性非霍奇金淋巴瘤非常罕见,仅有少数病例报道为起源于肝管分叉处的黏膜相关淋巴组织(MALT)淋巴瘤。我们在此报告一例女性患者,其肝门周围胆管被类似肝门部胆管癌的原发性MALT淋巴瘤阻塞,并对相关文献进行复习。

病例介绍

一名86岁女性因出现梗阻性黄疸和腹痛被转诊至我院。影像学检查显示肝内胆管扩张,肝总管包括分叉处狭窄,怀疑为胆管癌。最初实验室检查确诊为胆汁淤积,总胆红素为8.6mg/dL,天冬氨酸转氨酶(AST)178U/L,丙氨酸转氨酶(ALT)105U/L,肿瘤标志物CA 19-9升高至167U/mL。乙肝和丙肝病毒标志物均为阴性。她接受了肝外胆管切除及肝管空肠吻合术。切除标本的组织学检查显示为MALT淋巴瘤。术后1年的随访完全正常,无任何症状或疾病复发。

结论

在某些特殊情况下,尽管影像学和临床特征提示胆管癌,但梗阻性黄疸和腹痛的实际原因可能是非霍奇金淋巴瘤。对于MALT淋巴瘤,完整切除可治愈。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4a07/4919877/aced07c14acb/12957_2016_928_Fig1_HTML.jpg

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