| Literature DB >> 26137117 |
Meng-Ying Tong1, Xian Zhang2, Zhe Yu2, Xiu-Hua Sun2, Shuang Li1, Yang Zhang2.
Abstract
Primary bone lymphoma (PBL) is a rare disease, accounting for >1% of all cases of malignant lymphoma. Diffuse large B-cell lymphoma (DLBCL) is the most common histological type of PBL. The present study reported the case of a 68-year-old male with primary bone DLBCL, originally occurred in the sternum, which is a rare form of presentation. Computed tomography (CT), magnetic resonance imaging and bone emission CT were performed, followed by immunohistochemical analysis of a biopsy specimen, and the results were used to establish the diagnosis. At the time of diagnosis, no osseous involvement was observed. The clinical, radiological and histological features of PBL can mimic other medical conditions, thereby making the diagnosis difficult, and frequently leading to delays in treatment. The present study investigated the clinical features, management and prognosis of PBL, and reviewed previous relevant cases.Entities:
Keywords: diffuse large B-cell lymphoma; primary bone lymphoma; sternum
Year: 2015 PMID: 26137117 PMCID: PMC4473654 DOI: 10.3892/ol.2015.3122
Source DB: PubMed Journal: Oncol Lett ISSN: 1792-1074 Impact factor: 2.967