Pulmonary MALT lymphoma: A case report and review of the literature

被引：9
|
作者：
Bi, Lintao [1 ]
Li, Jun [1 ]
Dan, Wang [1 ]
Lu, Zhenxia [1 ]
机构：
[1] Jilin Univ, China Japan Union Hosp, Dept Hematol & Oncol, Changchun 130033, Jilin, Peoples R China
来源：
EXPERIMENTAL AND THERAPEUTIC MEDICINE | 2015年 / 9卷 / 01期
关键词：
mucosa-associated lymphoid tissue; lymphoma; pulmonary; B-CELL LYMPHOMA; TISSUE LYMPHOMA; INFECTION;
D O I：
10.3892/etm.2014.2072
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：
Mucosa-associated lymphoid tissue (MALT) lymphoma is an extranodal low-grade B-cell lymphoma. Pulmonary MALT lymphoma is considered to originate from bronchial MALT and is also referred to as bronchial-associated lymphoid tissue lymphoma. Pulmonary MALT lymphoma is a rare disease, but it is the most frequent subset of primary pulmonary lymphoma. The median age at diagnosis of pulmonary MALT lymphoma is 50-60 years, with only few patients aged <30 years. This is the case report of a 19-year-old patient with pulmonary MALT lymphoma presenting with a multiple pulmonary consolidation pattern on computed tomography scans, who underwent successful chemotherapeutic treatment with a chlorambucil-based regimen.
引用
收藏
页码：147 / 150
页数：4
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