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CASE REPORT
EBV-driven diffuse large B-cell lymphoma confined to the liver in a patient with a history of idiopathic CD4 lymphocytopenia
  1. Magdalena Dziadzio1,
  2. Ronnie Chee1,
  3. Christopher McNamara2,
  4. Maesha Deheragoda3,
  5. Thomas Wagner4,
  6. Suranjith L Seneviratne1
  1. 1Department of Immunology, Royal Free Hospital, London, UK
  2. 2Department of Haematology, Royal Free Hospital, London, UK
  3. 3Department of Cellular Pathology, Royal Free Hospital, London, UK
  4. 4Department of Nuclear Medicine, Royal Free Hospital, London, UK
  1. Correspondence to Dr Magdalena Dziadzio, magdalena.dziadzio{at}nhs.net

Summary

Idiopathic CD4 lymphocytopenia (ICL) is a rare immunodeficiency disorder. We describe a 49-year-old woman with a history of ICL who developed hepatic Epstein-Barr virus (EBV)-positive diffuse large B-cell lymphoma (DLBCL). ICL was diagnosed at a time of her presentation with varicella-zoster virus (VZV) meningoencephalitis and chorioretinitis. Her CD4 count subsequently improved but remained at the lower limits of the normal range. Five years later she presented with cough, fever and night-sweat. She was found to have multiple liver nodules on MRI, fluorodeoxyglucose (FDG) avid on the positron emission tomography (PET) CT, histologically defined as DLBCL, EBV positive and of non-germinal centre type. To our knowledge this is the first reported case of EBV-positive DLBCL localised to the liver in the context of ICL. EBV-positive DLBCL typically occurs in immunocompromised individuals. The corticosteroid therapy she received for VZV meningoencephalitis may have contributed to the EBV reactivation with subsequent EBV-driven malignant transformation of B-cells.

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