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Centroblastic lymphoma of the thyroid supervening long-lasting chronic lymphocytic leukemia (B-CLL) demonstration of biclonality by Immunohistochemical and gene rearrangement analysis

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Summary

A 67-year-old woman suffering since 5 years from a so far nontreated B-CLL underwent hemithyroidectomy for a rapidly enlarging tumor. Histologically, the coincidence of a centroblastic lymphoma and thyroidal infiltration by the CLL was diagnosed. Immunohistology revealed typical immunoprofils for both, B-CLL and centroblastic lymphoma on the background of B cell differentiation antigens. The bitypical immunoglobulin light chain expression — λ on the B-CLL cells and κ on the centroblasts — suggested biclonality. This was confirmed by gene rearrangement analysis of peripheral leukemia cells and tumor tissue. Thus, the final diagnosis of a primary thyroidal lymphoma of the centroblastic type (stage IE) arising independently from a preexisting B-CLL was achieved. Consequently, the patient received local radiotherapy.

In our opinion, the designation “Richter's Syndrome”, readily applied in the literature, is inappropriate for this tumor constellation.

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Abbreviations

AEC:

3-amino-9-ethylcarbazole

B-CLL:

B-chronic lymphocytic leukemia

CB:

centroblastic lymphoma

CD:

clusters of monoclonal antibodies to leucocyte differentiation antigens

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Supported by the Tumorzentrum Heidelberg/Mannheim

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Trümper, L., Matthaei-Maurer, D.U., Knauf, W. et al. Centroblastic lymphoma of the thyroid supervening long-lasting chronic lymphocytic leukemia (B-CLL) demonstration of biclonality by Immunohistochemical and gene rearrangement analysis. Klin Wochenschr 66, 736–742 (1988). https://doi.org/10.1007/BF01726417

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  • DOI: https://doi.org/10.1007/BF01726417

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