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