Abstract:
:Primary hepatic lymphoma (PHL) is an uncommon lymphoid tumor with varied clinical features and treatment outcome. In the present study, the case of a 56-year-old patient with PHL and no clinical presentation was reported. During a routine physical examination, multiple hypodense nodules were incidentally detected in right lobes of the liver and hepatic portal in an abdominal computed tomography scan. A liver biopsy revealed the presence of a non-Hodgkin's lymphoma diffuse large B cell type that was CD20-positive, followed by the diagnosis of a PHL. The patient was treated with R-CHOP, radiotherapy and R-Hyper-CVAD/R-HD MTX-ara-C, and complete remission was achieved.
journal_name
Oncol Lettjournal_title
Oncology lettersauthors
Zhang KJ,Chen S,Chen JL,Dong LHdoi
10.3892/ol.2015.2920subject
Has Abstractpub_date
2015-04-01 00:00:00pages
1557-1560issue
4eissn
1792-1074issn
1792-1082pii
ol-09-04-1557journal_volume
9pub_type
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