| Literature DB >> 28561533 |
Siobhan Glavey1, John Quinn1, Mary McCloy2, Jeremy Sargent2, Yvonne McCartney3, Mark Catherwood4, Teresa Marafioti5, Mary Leader3, Philip Murphy1, Patrick Thornton1.
Abstract
Chronic lymphocytic leukaemia (CLL) is a chronic B-cell lympho-proliferative disorder in which lymphomatous transformations occur in 5%-15% of patients. Histologically these cases resemble diffuse large B-cell lymphoma, or Richter's transformation, in over 80% of cases. Rare cases of transformation to Hodgkin lymphoma (HL) have been reported in the literature with an estimated prevalence of 0.4%. We report a case of a 67-year-old female with CLL treated with the novel Bruton's tyrosine kinase (Btk) inhibitor, ibrutinib, who subsequently presented with intractable fevers. Bone marrow trephine, and lymph node biopsy revealed classical HL with negative immuno-histochemistry for Btk in HL cells, on a backdrop of CLL. The patient commenced treatment with Adriamycin, Vinblastine and Dacarbazine (AVD), which resulted in an excellent response. Hodgkin transformation of CLL is rare with a single retrospective study of 4121 CLL patients reporting only 18 cases. Btk expression in HL cells is recently recognised in classical HL; however, the majority of HLs are Btk negative. Given that Btk inhibitors have recently been shown to induce genomic instability in B cells, in the context of their widespread use, such emerging cases are increasingly relevant.Entities:
Keywords: Hodgkin lymphoma; chronic lymphocytic leukaemia
Mesh:
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Year: 2017 PMID: 28561533 DOI: 10.1111/ejh.12911
Source DB: PubMed Journal: Eur J Haematol ISSN: 0902-4441 Impact factor: 2.997