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Primary Hepatic Extranodal Marginal Zone Lymphoma of Mucosa-Associated Lymphoid Tissue in a Patient with Chronic Hepatitis B Virus Infection: Case Report and Summary of the Literature

机译:慢性乙型肝炎病毒感染患者粘膜相关淋巴组织的原发性肝外淋巴瘤:病例报告和文献综述

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摘要

Background: The incidence of extranodal marginal zone lymphoma of mucosa-associated lymphoid tissue (MALT lymphoma) is low, at 7–8% of all non-Hodgkin lymphoma cases. The most common site of MALT lymphoma occurrence is the stomach. Primary hepatic extranodal marginal zone lymphoma of MALT is classified as a type of non-gastric MALT lymphoma and is considered extremely rare, with no consensus on imaging study findings or treatment due to a limited number of reports. We herein describe a rare case of primary hepatic extranodal marginal zone lymphoma of MALT with underlying hepatitis B infection (HBV) and present useful diagnostic findings of various imaging modalities, including contrast-enhanced ultrasonography (CEUS) with Sonazoid. Case presentation: A 66-year-old woman was diagnosed as being a non-active carrier of HBV at 51 years of age at the time of total hysterectomy and bilateral adnexectomy for uterine cervical cancer. She was admitted to our hospital following the incidental detection of two focal liver lesions on computed tomography. The lesions were considered malignant based on clinical and other radiologic imaging findings. Her CEUS results of hypo-enhancement in the portal and late phases were consistent with those of previously reported cases of hepatic extranodal marginal zone lymphoma of MALT, and histological liver biopsy findings were compatible with the diagnosis. Conclusions: Primary hepatic extranodal marginal zone lymphoma of MALT is a rare condition that can appear in HBV carriers. Characteristic CEUS findings may help in disease diagnosis. Clinicians should bear primary hepatic extranodal marginal zone lymphoma of MALT in mind when encountering patients with focal liver lesions which exhibit image findings different from those of typical hepatocellular carcinoma.
机译:背景:粘膜相关淋巴组织(麦芽淋巴瘤)的外槽边缘区淋巴瘤的发生率低,占所有非霍奇金淋巴瘤病例的7-8%。麦芽淋巴瘤的最常见现场是胃。麦芽的原发性肝外胚间区域淋巴瘤被归类为一种非胃麦芽淋巴瘤,被认为是极其罕见的,而没有关于成像研究结果或由于报告数量有限的成像或治疗。我们在此描述了罕见的丙肝炎感染(HBV)的麦芽麦芽原发性肝外边缘区淋巴瘤的罕见案例,并提出了各种成像模态的有用诊断结果,包括具有SONAZOID的对比增强的超声检查(CEUS)。案例介绍:一名66岁的女性被诊断为HBV的非活跃载体,在总子宫切除术和双侧宫颈癌的两侧肝切除术时期为51岁。在偶然的两个局灶性肝病变的偶然检测偶然检测后,她被院入院。基于临床和其他放射学成像发现,病变被认为是恶性的。她的CEUS在门静脉和晚期阶段的Hypo-ass的结果与先前报告的肝外部边缘区淋巴瘤的患者的患者符合,而组织学肝活组织检查结果与诊断相容。结论:麦芽原发性肝外胚间区域淋巴瘤是一种罕见的病症,可以出现在HBV载体中。特征Ceus Coptings可能有助于疾病诊断。临床医生应在遇到患有局灶性肝脏病变的患者时涉及麦芽的原发性肝外淋巴瘤,其表现出不同于典型的肝细胞癌的图像结果。

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