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Primary Liver Lymphoma Presenting as Liver Nodules

机译:作为肝脏结节的原发性肝淋巴瘤

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摘要

The liver is usually affected in advanced stages of lympho­proliferative diseases, but primary liver lymphomas (PLLs) are rare. The diagnosis is usually late, especially in patients without identifiable risk factors, with consequent worse prognosis. We report the case of a 59-year-old female with progressive worsening pain in the right hypochondrium and weight loss. She was previously healthy and had a family history of gastrointestinal and gynecologic neoplasms. During the initial investigation, three liver nodules suggestive of liver metastases were found. Nevertheless, no primary neoplasm was identified in a subsequent evaluation with imaging and endoscopic exams. Laboratory exams excluded hepatic infections, metabolic diseases, and acquired immunosuppression. Biopsy of the lesions revealed diffuse large B-cell lymphoma. Lymph node and medullar involvement were excluded, and the diagnosis of PLL was assumed. The patient started chemotherapy with R-CHOP. With this case, we intend to alert for this differential diagnosis of liver nodules, even in the absence of predisposing conditions for lymphoma. We point out the need to define universal diagnosis criteria for this pathology.
机译:肝脏通常在淋巴抑制性疾病的高级阶段受到影响,但原发性肝淋巴瘤(PLL)是罕见的。诊断通常是晚期,特别是在没有可识别的危险因素的患者中,随之而来的预后较差。我们举报了一个59岁女性的案件,患有次次次闭孔和体重减轻的渐进性疼痛。她以前健康,并具有胃肠道和妇科肿瘤的家族史。在初步调查期间,发现了三种肝脏结节暗示肝脏转移。尽管如此,在随后的成像和内窥镜检查的后续评估中没有发现任何原发性肿瘤。实验室考试排除了肝脏感染,代谢疾病和获得免疫抑制。病变的活检显示弥漫性大B细胞淋巴瘤。排除淋巴结和髓质参与,并假设PLL的诊断。患者开始用R-Chec进行化疗。在这种情况下,我们打算提醒这种鉴别诊断肝结节,即使在没有促进淋巴瘤的情况下的情况下也是如此。我们指出需要为此病理学定义通用诊断标准。

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