Stepwise development of chromosomal abnormalities in angioimmunoblastic lymphadenopathy
Autor: | Brigitte Schlegelberger, Elisabeth Gödde, Karl Lennert, Werner Grote, Alfred C. Feller |
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Rok vydání: | 1990 |
Předmět: |
Male
Cancer Research medicine.medical_specialty Pathology Biology Genetics medicine Humans Molecular Biology Aged Chromosome Aberrations Cytogenetics Chromosome Karyotype Middle Aged medicine.disease Chromosome Banding Lymphoma Cell Transformation Neoplastic Chromosome 3 Immunoblastic Lymphadenopathy Karyotyping Immunology Monoclonal Chromosome abnormality Female Trisomy |
Zdroj: | Cancer Genetics and Cytogenetics. 50:15-29 |
ISSN: | 0165-4608 |
DOI: | 10.1016/0165-4608(90)90233-z |
Popis: | Cytogenetic studies of lymphoproliferative diseases, such as angioimmunoblastic lymphadenopathy (AILD), may provide a clue to the understanding of tumor development. Angioimmunoblastic lymphadenopathy may evolve from a nonmalignant lymphoproliferation into a peripheral T-cell lymphoma or even into a high-grade B-cell lymphoma and thus offers the chance to observe cytogenetic changes during lymphoma development. We report the cytogenetic findings in 24 cases of AILD. They are discussed together with 18 previously published cases from the same series [1]. A striking feature was that unrelated chromosome abnormalities, both clonal and nonclonal, were frequently observed. Eighteen of 25 cases with aberrant clones show trisomy 3 (a characteristic chromosome abnormality in peripheral T-cell lymphoma), trisomy 5, or both. This finding provides cytogenetic evidence that these cases are definitely peripheral T-cell lymphomas. From the results of the 42 cases, hypotheses of stepwise evolution of the chromosome abnormalities in AILD are deduced: the first step is the appearance of chromosome abnormalities in different cells because of a genetic instability. At this time, clonal proliferation of T cells was already demonstrated by the rearrangement of T-cell receptor genes. As a second step, chromosomally aberrant clones become established. A cytogenetically detectable monoclonal proliferation represents the third step. |
Databáze: | OpenAIRE |
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