Modern pathology : an official journal of the United States and Canadian Academy of Pathology, Inc · 2011
Clonally related histiocytic/dendritic cell sarcoma and chronic lymphocytic leukemia/small lymphocytic lymphoma: a study of seven cases.
СтатьяResearch Support, N.I.H., IntramuralНазвание и аннотация: Перевод пока не подготовлен
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Shao Haipeng, Xi Liqiang, Raffeld Mark, Feldman Andrew L, Ketterling Rhett P, Knudson Ryan, Rodriguez-Canales Jaime, Hanson Jeffrey, Pittaluga Stefania, Jaffe Elaine S
Аннотация
Histiocytic and interdigitating dendritic cell sarcomas are rare tumors originating from bone marrow-derived myeloid stem cells. Recent studies have shown evidence of cross-lineage transdifferentiation of B cells in follicular lymphoma to histiocytic and dendritic cell sarcomas. In this study, we report the morphologic, molecular and cytogenetic analysis of seven cases of chronic lymphocytic leukemia/small lymphocytic lymphoma (CLL/SLL) associated with histiocytic and dendritic cell sarcomas. All seven patients were elderly males (median age 71 years). The B-cell neoplasms preceded the development of the histiocytic and dendritic cell sarcomas in six of seven patients, and one patient had both tumors diagnosed at the same time. The tumors included four interdigitating dendritic cell sarcomas: one Langerhans cell sarcoma, one histiocytic sarcoma and one immature neoplasm with evidence of histiocytic origin. Laser-capture microdissection and PCR analysis showed identical clonal immunoglobulin gene rearrangements in the two phenotypically distinct components in all cases. There was a preferential usage of IGHV4-39 by the V-D-J gene rearrangement. By fluorescence in situ hybridization (FISH) analysis, two cases showed deletion 17p in both components, whereas four cases had normal cytogenetic findings by FISH in the CLL/SLL cells, but acquired cytogenetic abnormalities in the corresponding histiocytic and dendritic tumors. Chromosome 17p abnormalities were the most common cytogenetic abnormality detected in the sarcomas, seen in five of six cases studied. Compared with the CLL/SLL cells, the histiocytic/dendritic cells were largely negative for PAX5, but showed strong expression of PU.1 and variable and weak expression of CEBPβ. Our study provides evidence for transdifferentiation of CLL/SLL B cells to tumors of dendritic and less often histiocytic lineage, and suggests that secondary genetic events may play a role in this phenomenon.
Предметные рубрики MeSH
AgedAged, 80 and overBase SequenceBiomarkers, TumorCCAAT-Enhancer-Binding Protein-betaCell TransdifferentiationChromosome AberrationsChromosomes, Human, Pair 17Dendritic Cell Sarcoma, InterdigitatingGene Rearrangement, B-LymphocyteHistiocytic SarcomaHumansImmunohistochemistryIn Situ Hybridization, FluorescenceLangerhans Cell SarcomaLaser Capture MicrodissectionLeukemia, Lymphocytic, Chronic, B-CellMaleMarylandMiddle AgedMolecular Sequence DataPAX5 Transcription FactorPolymerase Chain ReactionProto-Oncogene ProteinsTrans-ActivatorsV(D)J RecombinationProto-Oncogene Protein Spi-1