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  • 1990-1994  (2)
  • 1
    Electronic Resource
    Electronic Resource
    Three Cambridge Center, Suite 208, Cambridge, MA 02142, USA : Blackwell Scientific Publications Inc.
    International journal of gynecological cancer 1 (1991), S. 0 
    ISSN: 1525-1438
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Medicine
    Notes: A total of 63 uterine leiomyomas were cytogenetically analyzed and, on neighboring tissue pieces, examined histologically. The tumors were dichotomized on the basis of their cellularity (29 normocellular and 34 hypercellular myomas) and on the absence (35 tumors) or presence (28 tumors) of mitoses (1–2 per 10 high-power fields). The cytogenetic analysis revealed normal karyotypes in 39 tumors and clonal chromosome abnormalities in 24. The latter group could be subdivided into cases with a single aberration (9 tumors), cases with more than one aberration but no subclones (8 tumors), and cases with multiple aberrations including subclones (7 tumors). Cytogenetically abnormal leiomyomas were more often hypercellular than cytogenetically normal tumors (17/24 = 71% versus 17/39 = 44%) and also more often had mitoses (16/24 = 67% versus 12/39 = 31%); these differences were statistically significant (p 〈 0.05). Within the group carrying chromosomal abnormalities, there was a direct linear tendency to the effect that karyotypically complex tumors were more often hypercellular and more often had mitotic figures: 4/9 = 44% of tumors with a single aberration were hypercellular and had mitoses compared with 5/8 = 63% for both parameters in the subgroup with several aberrations but only one clone. The cytogenetic subset characterized by the highest histologic activity were the 7 leiomyomas with clonal evolution giving rise to subclones; all these tumors were hypercellular and had mitoses.
    Type of Medium: Electronic Resource
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  • 2
    ISSN: 1573-7276
    Keywords: chromosome aberrations ; clonal evolution ; metastases ; soft tissue sarcomas
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: The karyotypic pattern at different stages of tumor development may provide information on tumor progression but few data are available regarding human solid tumors. Cytogenetic analysis was performed on the primary tumor and four lung metastases of a synovial sarcoma, and the primary tumor, two consecutive local recurrences, and six pulmonary metastases, obtained at two different occasions, of a malignant fibrous histiocytoma (MFH). Simultaneous existence of more than one cytogenetically aberrant clone was also assessed through analysis of more than one sample from the same surgical specimen. Clonal chromosome aberrations were detected in all samples from the synovial sarcoma, and in both local recurrences and five of the metastases from the MFH. All clones in both tumors were cytogenetically related. The primary synovial sarcoma tumor contained two clones, one of which was also found in the lung metastases, together with a third clone that had acquired additional aberrations. Four clones with a near-tetraploid chromosome number and complex aberrations were identified in the MFH. Likely evolutionary pathways could be deduced in both cases. In the patient with synovial sarcoma one of the pulmonary metastases, rather than the primary tumor, might well have been the source of another of the pulmonary metastases. In the MFH the cytogenetic findings indicated the presence of two co-existing lineages in the primary tumor, one giving rise to the local recurrences and one to the pulmonary metastases. Our findings show that cytogenetic analysis can be used to establish the chronologic relationships between different clones in primary tumors, local recurrences and distant metastases, to determine what genetic changes are of importance for the metastatic capability of tumor cells, and to help establish the origin of the metastatic lesions.
    Type of Medium: Electronic Resource
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