Diffuse large B-cell Lymphoma mimicking as cholangiocarcinoma in a young male presenting with obstructive jaundice

D. Muhammad, Khan Shoaib Ahmed, Samoon Dilnawaz, Majid Zain, H. Farina, Tassneem Abbas Ali, Luck Nasir Hasan
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Abstract

The involvement of bile duct in lymphoma is considered to be very rare and is usually a sequela of a disseminated disease [1]. In contrast to secondary involvement, primary non-Hodgkin’s lymphoma arising from the bile duct is extremely rare and presents with obstructive jaundice [2,3]. Non-Hodgkin’s lymphoma (NHL) accounts for 1% - 2% of all cases of malignant biliary obstruction [4]. Hepatobiliary involvement by malignant lymphoma is usually a secondary manifestation of systemic lymphoma. The first case of Non-Hodgkin lymphoma arising from bile duct was described by Nguyen in 1982 [5]. Most common extra nodal involvement of NHL is abdomen. Although, involvement of the stomach, pancreas or common bile duct is not common [6]. We present to you a case of 31year old male who presented to us with obstructive jaundice and was later diagnosed as Diffuse Large B-Cell lymphoma.
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弥漫大b细胞淋巴瘤模拟胆管癌的年轻男性表现为梗阻性黄疸
淋巴瘤累及胆管被认为是非常罕见的,通常是播散性疾病的后遗症[1]。与继发性累及相比,起源于胆管的原发性非霍奇金淋巴瘤极为罕见,表现为梗阻性黄疸[2,3]。非霍奇金淋巴瘤(Non-Hodgkin’s lymphoma, NHL)占所有恶性胆道梗阻病例的1% - 2%[4]。恶性淋巴瘤累及肝胆通常是全身性淋巴瘤的继发表现。首例胆管非霍奇金淋巴瘤由Nguyen于1982年报道[5]。NHL最常见的淋巴结外受累是腹部。虽然,累及胃、胰腺或胆总管并不常见[6]。我们向您报告一例31岁男性患者,他向我们提出梗阻性黄疸,后来被诊断为弥漫性大b细胞淋巴瘤。
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