Primary hepatic lymphoma: a rare case report and literature review

被引:0
作者
Li, Ke [2 ]
Luo, Runlan [1 ]
Xiong, Zuming [2 ]
Xu, Jinming [2 ]
Fang, Dengyang [2 ]
机构
[1] Fuling Cent Hosp Chongqing City, Dept Ultrasound, Chongqing, Peoples R China
[2] Fuling Cent Hosp Chongqing City, Dept Gen Surg, Chongqing, Peoples R China
来源
INTERNATIONAL JOURNAL OF CLINICAL AND EXPERIMENTAL MEDICINE | 2019年 / 12卷 / 03期
关键词
Lymphoma; non-hodgkin; lymphoma; large B-cell; diffuse; liver neoplasms; NON-HODGKINS-LYMPHOMA; B-CELL LYMPHOMA; LIVER; RITUXIMAB;
D O I
暂无
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Primary hepatic lymphoma (PHL) is a rare malignancy, which only occupies about 0.4% of all primary extranodal non-Hodgkin lymphomas (NHLs) and 0.016% of all NHLs. It includes B-cell lymphoma, T-cell lymphoma, and others. A seventy-one year old man first went to visit the doctor because of pneumonia and then he was diagnosed with PHL of diffuse large B-cell lymphoma with no virus hepatitis or other typical symptoms. PHL is a rare disease, which is very difficult to diagnose due to non-specific clinical manifestations and accessory examinations. This case may help clinicians to improve their understanding of this disease.
引用
收藏
页码:2827 / 2832
页数:6
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