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Please use this identifier to cite or link to this item: http://acervodigital.unesp.br/handle/11449/128349
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dc.contributor.authorSun, Sue Yazaki-
dc.contributor.authorMelamed, Alexander-
dc.contributor.authorGoldstein, Donald P.-
dc.contributor.authorBernstein, Marilyn R.-
dc.contributor.authorHorowitz, Neil S.-
dc.contributor.authorMoron, Antonio Fernandes-
dc.contributor.authorMaesta, Izildinha-
dc.contributor.authorBraga, Antonio-
dc.contributor.authorBerkowitz, Ross S.-
dc.date.accessioned2015-10-21T13:09:11Z-
dc.date.accessioned2016-10-25T20:59:23Z-
dc.date.available2015-10-21T13:09:11Z-
dc.date.available2016-10-25T20:59:23Z-
dc.date.issued2015-07-01-
dc.identifierhttp://www.sciencedirect.com/science/article/pii/S0090825815008719-
dc.identifier.citationGynecologic Oncology. San Diego: Academic Press Inc Elsevier Science, v. 138, n. 1, p. 46-49, 2015.-
dc.identifier.issn0090-8258-
dc.identifier.urihttp://hdl.handle.net/11449/128349-
dc.identifier.urihttp://acervodigital.unesp.br/handle/11449/128349-
dc.description.abstractObjective. To compare the clinical presentation and incidence of postmolar gestational trophoblastic neoplasia (GTN) among recent (1994-2013) and historical (1988-1993) cases of complete hydatidiform mole (CHM).Methods. This study included two non-concurrent cohorts (1988-1993 versus 1994-2013) of patients from the New England Trophoblastic Disease Center (NETDC). Clinical and pathologic reports of patients diagnosed with CHM between 1994 and 2013 were reviewed. Gestational age at evacuation, features of clinical presentation, human chorionic gonadotropin (hCG) levels, and the rate of progression to GTN were compared.Results. In the current cohort (1994 to 2013) the median gestational age at diagnosis continued to decline compared to our prior cohort (1988-1993) (9 weeks versus 12 weeks). Patients from the current cohort were significantly more likely to be diagnosed prior to the 11th week of gestation (56 versus 41%, p = 0.04). Patients in the current cohort were also significantly less likely to present with vaginal bleeding (46 versus 84%, p < 0.001). Earlier diagnosis of complete mole did not result in a decrease in the rate of postmolar GTN. The frequencies of postmolar GTN in the current (1994-2013) and prior (1988-1993) cohorts were 19 and 23%, respectively. In the current cohort, even diagnosis prior to ten weeks gestation did not decrease the risk of developing GTN.Conclusions. This study indicates that complete mole continues to be diagnosed progressively earlier resulting in a further decrease in some classical presenting symptoms. However, despite earlier detection, the risk of development of postmolar GTN has not been affected. (C) 2015 Elsevier Inc. All rights reserved.en
dc.description.sponsorshipConselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq)-
dc.description.sponsorshipDyett Family Trophoblastic Disease Research and Registry Endowment-
dc.format.extent46-49-
dc.language.isoeng-
dc.publisherElsevier B.V.-
dc.sourceWeb of Science-
dc.subjectGestational trophoblastic diseaseen
dc.subjectGestational trophoblastic neoplasiaen
dc.titleChanging presentation of complete hydatidiform mole at the New England Trophoblastic Disease Center over the past three decades: does early diagnosis alter risk for gestational trophoblastic neoplasia?en
dc.typeoutro-
dc.contributor.institutionUniversidade Federal de São Paulo (UNIFESP)-
dc.contributor.institutionBrigham &Womens Hosp-
dc.contributor.institutionUniversidade Estadual Paulista (UNESP)-
dc.contributor.institutionDonald P Goldstein MD Trophoblast Tumor Registry-
dc.contributor.institutionUniversidade Federal do Rio de Janeiro (UFRJ)-
dc.contributor.institutionUniversidade Federal Fluminense (UFF)-
dc.contributor.institutionHarvard Canc Ctr-
dc.contributor.institutionHarvard Univ-
dc.description.affiliationUNIFESP Sao Paulo Fed Univ, Paulista Sch Med, Dept Obstet, Sao Paulo, SP, Brazil-
dc.description.affiliationBrigham &Womens Hosp, Dept Obstet &Gynecol, Div Gynecol Oncol, Boston, MA 02115 USA-
dc.description.affiliationUNESP Sao Paulo State Univ, Botucatu Med Sch, Dept Gynecol &Obstet, Botucatu, SP, Brazil-
dc.description.affiliationDonald P Goldstein MD Trophoblast Tumor Registry, New England Trophoblast Dis Ctr, Boston, MA USA-
dc.description.affiliationUNIFESP Sao Paulo Fed Univ, Paulista Sch Med, Trophoblast Dis Ctr, Sao Paulo Hosp, Sao Paulo, SP, Brazil-
dc.description.affiliationUNESP Sao Paulo State Univ, Botucatu Med Sch, Trophoblast Dis Ctr, Botucatu, SP, Brazil-
dc.description.affiliationUniv Fed Rio de Janeiro, Matern Sch, Trophoblast Dis Ctr, Rio De Janeiro, Brazil-
dc.description.affiliationUniv Fed Fluminense, Antonio Pedro Univ Hosp, Trophoblast Dis Ctr, Rio De Janeiro, Brazil-
dc.description.affiliationHarvard Canc Ctr, Dana Farber Canc Inst, Boston, MA USA-
dc.description.affiliationHarvard Univ, Sch Med, Boston, MA USA-
dc.description.affiliationUnespUNESP Sao Paulo State Univ, Botucatu Med Sch, Dept Gynecol &Obstet, Botucatu, SP, Brazil-
dc.description.affiliationUnespUNESP Sao Paulo State Univ, Botucatu Med Sch, Trophoblast Dis Ctr, Botucatu, SP, Brazil-
dc.description.sponsorshipIdCNPq: 200756/2014-1-
dc.identifier.doihttp://dx.doi.org/10.1016/j.ygyno.2015.05.002-
dc.identifier.wosWOS:000356841100008-
dc.rights.accessRightsAcesso restrito-
dc.relation.ispartofGynecologic Oncology-
Appears in Collections:Artigos, TCCs, Teses e Dissertações da Unesp

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