Complete response to comprehensive treatment of a primary hepatic diffuse large B cell lymphoma: A case report

Oncology Letters
Kai Jing ZhangLi Hua Dong

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.

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Citations

Feb 6, 2021·Gastroenterology·Isaac E PerryJohn Erikson Yap
Sep 27, 2020·Journal of Medical Case Reports·Eduardo DantasAna Paula Oliveira

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Methods Mentioned

BETA
biopsy
surgical resection

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