Li Yunlong, Zhou Liangrui, Zhang Ning, Wei Yuchen, Yang Chen, Liu Xiaohong, Kang Lin
Department of Internal Medicine, Peking Union Medical College Hospital, Peking Union Medical College, Chinese Academy of Medical Sciences, Beijing, CHN.
Department of Pathology, Peking Union Medical College Hospital, Peking Union Medical College, Chinese Academy of Medical Sciences, Beijing, CHN.
Cureus. 2024 Jul 26;16(7):e65472. doi: 10.7759/cureus.65472. eCollection 2024 Jul.
Mucosa-associated lymphoid tissue (MALT) lymphoma is a low-grade malignant lymphoproliferative disease, representing a low percentage of newly diagnosed lymphoma cases. Although its exact cause is still unclear, it is commonly associated with infections or autoimmune diseases. The stomach is the most frequent site for MALT lymphoma, with primary hepatic MALT lymphoma being exceptionally rare. Cases of primary hepatic MALT lymphoma often coincide with viral hepatitis. In this report, we present a case of primary hepatic MALT lymphoma in a patient with no history of hepatitis but complicated by primary biliary cholangitis (PBC) and Hashimoto's thyroiditis.
黏膜相关淋巴组织（MALT）淋巴瘤是一种低度恶性的淋巴增殖性疾病，在新诊断的淋巴瘤病例中占比很低。尽管其确切病因尚不清楚，但通常与感染或自身免疫性疾病有关。胃是MALT淋巴瘤最常见的发病部位，原发性肝MALT淋巴瘤极为罕见。原发性肝MALT淋巴瘤病例常与病毒性肝炎同时出现。在本报告中，我们呈现了一例原发性肝MALT淋巴瘤患者，该患者无肝炎病史，但合并原发性胆汁性胆管炎（PBC）和桥本甲状腺炎。
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