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酷似肝门部胆管癌的原发性肝外胆管淋巴瘤,对化疗反应显著

Primary extrahepatic bile duct lymphoma mimicking Klatskin's tumor, dramatic response to chemotherapy.

作者信息

Mikail Cakir, Sefa Tuzun, Tamer Karsidag, Anil Savas Osman, Gulcin Yegen

机构信息

Ministry of Health, Haseki Research and Training Hospital, General Surgery Department, Istanbul, Turkey.

Ministry of Health, Haseki Research and Training Hospital, General Surgery Department, Istanbul, Turkey.

出版信息

Int J Surg Case Rep. 2015;8C:147-9. doi: 10.1016/j.ijscr.2015.01.034. Epub 2015 Jan 21.

Abstract

INTRODUCTION

Non- Hodgkin's lymphoma (NHL) mimicking Klatskin's tumor is rare but possible. It can be confused with tumors for which major surgery is needed. Imaging modalities have similar features in Klatskin's tumor and non-Hodgkin's lymphoma.

PRESENTATION OF CASE

We herein report a patient who was first thought having a Klatskin's tumor and prepared for major surgery. A month later, obstructive jaundice developed and a second magnetic resonance-magnetic resonance cholangiopancreotography showed a doubling size of the tumor in one month. In terms of tumor behavior, lymphoma was suspected and a tru-cut biopsy was performed by interventional radiology. Pathological examinations revealed non-Hodgkin's lymphoma large B-cell type. After 4 cycles of chemotherapy by hematology-oncology department, complete cure was achieved.

DISCUSSION

Since the radiologic and clinical features are confusable in Klatskin's tumor and non-Hodgkin lymphoma. Tumor biologic behavior and other biochemical parameters together may put a suspicion in mind. Upon suspicion biopsy must be done radiologically.

CONCLUSION

Primary liver lymphoma arising from the bile ducts is extremely rare and radiologic imaging features do not differ from cholangiocarcinoma. A strong suspicion may prevent unnecessary surgery. Since the treatment of non-Hodgkin's lymphoma is mainly chemotherapy.

摘要

引言

非霍奇金淋巴瘤(NHL)酷似肝门部胆管癌虽罕见但有可能。它可能会与需要进行大手术的肿瘤相混淆。在肝门部胆管癌和非霍奇金淋巴瘤中,影像学检查具有相似特征。

病例介绍

我们在此报告一名患者,最初被认为患有肝门部胆管癌并准备进行大手术。一个月后,出现梗阻性黄疸,第二次磁共振-磁共振胰胆管造影显示肿瘤在一个月内增大了一倍。就肿瘤行为而言,怀疑为淋巴瘤,介入放射科进行了粗针活检。病理检查显示为非霍奇金淋巴瘤大B细胞型。血液肿瘤科进行4个周期化疗后实现了完全治愈。

讨论

由于肝门部胆管癌和非霍奇金淋巴瘤的放射学和临床特征容易混淆。肿瘤生物学行为和其他生化参数可能会引发怀疑。一旦怀疑,必须通过放射学方法进行活检。

结论

起源于胆管的原发性肝淋巴瘤极为罕见,其放射学影像特征与胆管癌无异。高度怀疑可避免不必要的手术。由于非霍奇金淋巴瘤的治疗主要是化疗。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4cf0/4353956/a4f22adf827e/gr1.jpg

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