Primary hepatic peripheral T‑cell lymphoma: A case report

  • Authors:
    • Hui‑Juan Hu
    • Mei‑Yan Liao
    • Yan‑Juan Qu
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  • Published online on: May 7, 2014     https://doi.org/10.3892/ol.2014.2119
  • Pages: 258-262
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Abstract

Primary hepatic peripheral T‑cell lymphoma (PHL) is extremely rare. A case of primary hepatic peripheral T‑cell lymphoma of a 59‑year‑old male is presented in the current study. PHL lesions are diagnosed by the existence of a hepatic mass, in the absence of lymphadenopathy, splenomegaly or bone marrow involvement associated with normal tumor markers. Treatment options are surgical resection and subsequent chemotherapy. Histopathological examination by immunohistochemical staining of the tissue biopsies at laparotomy confirmed a diagnosis of PHL.
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July-2014
Volume 8 Issue 1

Print ISSN: 1792-1074
Online ISSN:1792-1082

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Spandidos Publications style
Hu HJ, Liao MY and Qu YJ: Primary hepatic peripheral T‑cell lymphoma: A case report. Oncol Lett 8: 258-262, 2014.
APA
Hu, H., Liao, M., & Qu, Y. (2014). Primary hepatic peripheral T‑cell lymphoma: A case report. Oncology Letters, 8, 258-262. https://doi.org/10.3892/ol.2014.2119
MLA
Hu, H., Liao, M., Qu, Y."Primary hepatic peripheral T‑cell lymphoma: A case report". Oncology Letters 8.1 (2014): 258-262.
Chicago
Hu, H., Liao, M., Qu, Y."Primary hepatic peripheral T‑cell lymphoma: A case report". Oncology Letters 8, no. 1 (2014): 258-262. https://doi.org/10.3892/ol.2014.2119