Interphase fluorescence in situ hybridization with an IGH probe is important in the evaluation of patients with a clinical diagnosis of chronic lymphocytic leukaemia

G. S. Nowakowski, G. W. Dewald, J. D. Hoyer, S. F. Paternoster, K. J. Stockero, S. R. Fink, S. A. Smoley, E. D. Remstein, R. L. Phyliky, T. G. Call, T. D. Shanafelt, N. E. Kay, Clive S. Zent

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48 Scopus citations


Translocations involving IGH are common in some lymphoid malignancies but are believed to be rare in chronic lymphocytic leukaemia (CLL). To study the clinical utility of fluorescence in situ hybridization (FISH) for IGH translocations, we reviewed 1032 patients with a presumptive diagnosis of CLL. Seventy-six (7%) patients had IGH translocations. Pathology and clinical data were available for the 24 patients evaluated at the Mayo Clinic. Ten (42%) patients had IGH/cyclin D1 fusion and were diagnosed with mantle cell lymphoma (MCL). The immunophenotype was typical of MCL in three of these patients and atypical for MCL in seven patients. One patient had biclonal disease with typical MCL and CLL with IGH/BCL-2. Eleven (46%) patients had IGH/BCL-2 fusion including the patient with biclonal disease. Two of these patients had leukaemic phase follicular lymphoma and nine patients had CLL. The median progression-free survival of patients with CLL and IGH/BCL-2 translocation was 20-6 months. The two patients with IGH/BCL-3 fusion (one of these also had IGH/BCL-11a) had rapid disease progression. The IGH partner gene was not identified in two patients. We conclude that use of an IGH probe in FISH analysis of monoclonal B-cell lymphocytosis improves diagnostic precision and could have prognostic value in patients with CLL.

Original languageEnglish (US)
Pages (from-to)36-42
Number of pages7
JournalBritish journal of haematology
Issue number1
StatePublished - Jul 1 2005



  • BCL-2
  • CLL
  • FISH
  • IGH
  • Translocations

ASJC Scopus subject areas

  • Hematology

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