一例预后不良的胆道髓外浆细胞瘤

IF 0.8 Q3 MEDICINE, GENERAL & INTERNAL
Eiko Sakurai, Kazunori Nakaoka, S. Yamada, Naoe Goto, A. Tomita, Y. Hirooka, T. Tsukamoto
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引用次数: 0

摘要

髓外浆细胞瘤(EMP)是一种罕见的疾病,由骨骼以外的组织中存在的单克隆浆细胞组成。大多数EMP位于头部和颈部。我们报告了一例极为罕见的EMP源于一名76岁男性的胆道。这是第五例胆道原发性EMP的报告。他被诊断为黄疸,并被转诊接受额外检查。腹部超声检查显示胆囊和胆管中有一个肿瘤,并通过内镜超声引导细针抽吸(EUS-FNA)进行胆管活检。病理和免疫组织化学检查显示,该肿瘤是起源于胆道的浆细胞瘤。尽管进行了内镜胆道引流,但由于肿瘤引起的梗阻性黄疸,胆管感染没有得到很好的控制。此外,化疗期间肿瘤出血未得到控制。采用胰十二指肠切除术和胆囊切除术控制感染和出血。尽管术后继续化疗,但肝内胆管肿瘤扩大。他在确诊后7个月死于难治性肿瘤。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
A Case of Extramedullary Plasmacytoma of the Biliary Tract with a Poor Prognosis
Extramedullary plasmacytoma (EMP) is a rare disease consisting of the presence of monoclonal plasma cells in tissues other than the bone. Most EMPs are located in the head and neck region. We present an extremely rare case of an EMP originating from the biliary tract in a 76-year-old male. This is the fifth report of a primary EMP arising from the biliary tract. He was diagnosed with jaundice, and he was referred for an additional examination. Abdominal ultrasonography revealed a tumor in the gallbladder and bile ducts, and a bile duct biopsy was performed via endoscopic ultrasound-guided fine-needle aspiration (EUS-FNA). The pathological and immunohistochemical examination revealed that the tumor was a plasmacytoma originating in the biliary tract. Although endoscopic biliary drainage was performed, the bile duct infection was not well controlled due to obstructive jaundice caused by the tumor. Furthermore, the bleeding from the tumor during chemotherapy was uncontrolled. Pancreaticoduodenectomy and cholecystectomy were performed to control the infection and bleeding. Although chemotherapy was continued after surgery, the tumor of the intrahepatic bile duct enlarged. He died seven months after the diagnosis because of the treatment-resistant tumor.
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