Excellent prognosis and prevalence of HCV infection of primary hepatic and splenic non-Hodgkin's lymphoma

Eur J Haematol. 2008 Jul;81(1):51-7. doi: 10.1111/j.1600-0609.2008.01081.x. Epub 2008 Apr 4.

Abstract

Background: Primary Hepatic (PHL) and Primary Splenic (PSL) non-Hodgkin's Lymphoma are rare entities. Small series of PHL and PSL have been reported, suggesting a non-fortuitous association with Hepatitis C Virus (HCV) infection. The prognosis is believed to be dismal, with early recurrence and short survival.

Patients: We retrospectively reviewed all PHL and PSL patients diagnosed at our institution between 1990 and 2005.

Results: Twenty-five adult patients were identified, six with PHL and 19 with PSL. Twenty-four patients had a B-cell lymphoma, defined as Diffuse Large B-cell lymphoma in 18. The prevalence of HCV infection was 68% among PSL and 66% among PHL. Combination chemotherapy was the mainstay of treatment for PHL and PSL; all but one patient with PSL underwent splenectomy before chemotherapy. Complete remission was achieved in all the cases after frontline therapy; only four patients relapsed but responded to additional chemotherapy courses. Most patients presented with aggressive histological subtypes; 92% were alive at a median follow up of 79 months. HCV infection did not appear to influence the results of therapy.

Conclusion: Our study confirms the rarity of PHL and PSL, shows a high prevalence of HCV infection, and demonstrates that the outcome of patients with PHL and PSL may be favourable.

MeSH terms

  • Aged
  • Antineoplastic Combined Chemotherapy Protocols / therapeutic use
  • Female
  • Follow-Up Studies
  • Hepatitis C / complications*
  • Humans
  • Liver Neoplasms / drug therapy
  • Liver Neoplasms / etiology
  • Liver Neoplasms / virology*
  • Lymphoma, Large B-Cell, Diffuse
  • Lymphoma, Non-Hodgkin / drug therapy
  • Lymphoma, Non-Hodgkin / etiology
  • Lymphoma, Non-Hodgkin / virology*
  • Male
  • Middle Aged
  • Prevalence
  • Prognosis
  • Recurrence
  • Remission Induction
  • Retrospective Studies
  • Splenic Neoplasms / drug therapy
  • Splenic Neoplasms / etiology
  • Splenic Neoplasms / virology*
  • Survival Rate