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Obstet Gynecol ; 79(5 ( Pt 2)): 849-53, 1992 May.
Artigo em Inglês | MEDLINE | ID: mdl-1565385

RESUMO

Patients with dysgenetic gonads and Turner syndrome are unlikely to develop endometrial carcinoma unless they have received unopposed estrogen replacement therapy. This case describes a 54-year-old woman with Turner syndrome and primary amenorrhea who developed adenocarcinoma of the endometrium without having received hormone replacement. Vaginal bleeding, a pelvic mass, and sepsis were the presenting symptoms. The patient also had diabetes mellitus and hypothyroidism. Polyglandular endocrine patterns are known to occur with a high frequency in these patients. The woman's chromosome studies revealed a modified 46,X,i(Xq) (isochromosome X). This is the first report of an isochromosome X patient to develop endometrial cancer without receiving estrogen replacement. The etiology of this rare case may be an increased propensity for patients with X-chromosome deletions to develop neoplasms in general, or extragonadal estrogen production.


Assuntos
Adenocarcinoma/complicações , Diabetes Mellitus Tipo 2/complicações , Neoplasias do Endométrio/complicações , Terapia de Reposição de Estrogênios , Síndrome de Turner/complicações , Terapia de Reposição de Estrogênios/efeitos adversos , Feminino , Humanos , Pessoa de Meia-Idade , Fatores de Risco
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