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1.
Cancer Genet Cytogenet ; 78(2): 172-4, 1994 Dec.
Artículo en Inglés | MEDLINE | ID: mdl-7828149

RESUMEN

We analyzed 45 pelvic endometrial implants from 42 patients between the ages of 14 and 40 years to investigate whether cytogenetic abnormalities were present in these samples. Chromosomal abnormalities have been described in benign tumors of the female genital tract, such as uterine leiomyomas and endometrial polyps. Furthermore, heritable factors have been postulated to influence a woman's susceptibility to develop endometrial tissue implants outside the uterine cavity. To study whether these factors result in or are associated with chromosomal changes, endometriosis cells were analyzed cytogenetically after short-term culture. No consistent chromosome abnormalities were observed in any of the cases analyzed.


Asunto(s)
Aberraciones Cromosómicas , Endometriosis/genética , Enfermedades Peritoneales/genética , Adulto , Femenino , Humanos , Cariotipificación
3.
Cancer Genet Cytogenet ; 53(1): 125-36, 1991 May.
Artículo en Inglés | MEDLINE | ID: mdl-2036633

RESUMEN

Cytogenetic analysis of short-term cultures from 35 leiomyomas of the female genitourinary tract showed abnormal karyotypes in 14 cases. In 11 of 14 aberrant tumors, normal cells were also observed. Structural changes were most frequent, resulting in modal chromosome numbers in the diploid range. Our data confirm preferential breakpoint clusters at 7q, 12q14-15, and 14q23-24, mainly resulting from consistent, specific chromosome rearrangements such as t(12;14)(q14-15;q23-24) and del(7)(q21) or del(7)(q22q32). Together with previously published cases, we describe trisomy 12, ring chromosomes, and monosomy 22 as new additional recurrent findings in myomas. Statistical analyses of possible coherencies between tumor karyotype (abnormal versus normal) and clinicopathologic data, as well as age of the patients, menopausal status, and tumor size showed no correlations.


Asunto(s)
Aberraciones Cromosómicas , Leiomioma/genética , Neoplasias Urogenitales/genética , Adulto , Femenino , Humanos , Cariotipificación , Persona de Mediana Edad
4.
Cancer Genet Cytogenet ; 41(1): 99-103, 1989 Aug.
Artículo en Inglés | MEDLINE | ID: mdl-2766256

RESUMEN

A benign endometrial polyp from a 50-year-old postmenopausal woman has been cytogenetically investigated. A single clonal karyotypic anomaly, inv(12)(p11.2q13), was found in about 30% of cells analyzed after short-term culture. This finding contributes further to the hypothesis that the chromosomal segment 12q13-q14, which is also involved in chromosomal rearrangements in uterine leiomyomas, pleomorphic adenomas of the salivary glands, lipomas, and myxoid liposarcomas, contains a gene or genes that are related to cellular proliferation rather than to malignant transformation.


Asunto(s)
Inversión Cromosómica , Cromosomas Humanos Par 12 , Pólipos/genética , Neoplasias Uterinas/genética , Bandeo Cromosómico , Femenino , Humanos , Cariotipificación , Persona de Mediana Edad , Pólipos/patología , Neoplasias Uterinas/patología
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