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Tumor de células de Leydig do ovário: caso clínico

dc.contributor.authorSaleiro, S
dc.contributor.authorGonçalves, S
dc.contributor.authorMarinho, C
dc.contributor.authorRebelo, T
dc.contributor.authorManarte, A
dc.contributor.authorOliveira, CF
dc.date.accessioned2010-03-02T15:17:38Z
dc.date.available2010-03-02T15:17:38Z
dc.date.issued2009
dc.description.abstractLeydig cell tumours account for 0.1% of all ovarian tumours and are a type of steroid cell tumour. According to the World Health Organisation they are classified in the group of sex cord stromal tumours. The clinical presentation is usually a hyperandrogenic state with signs of virilisation, but occasionally patients may exhibit a hyperestrogenic state. The tumour has a benign behaviour, with an excellent prognosis and reversion of symptoms after treatment. The authors present the case of a 61 year-old woman with signs of virilisation that started 8 months before. Abdomino-pelvic computerized tomography showed an enlarged left ovary, while blood hormone analisys revealed increased levels of testosterone, androstenedione and 17-OH progesterone. The patient was submitted to laparoscopic bilateral oophorectomy. Histological examination revealed a Leydig cell tumour of the left ovary. After surgery there was complete regression of symptoms and normalisation of sex hormone levels.pt
dc.identifier.citationActa Obstet Ginecol Port 2009;3(4):217-20pt
dc.identifier.urihttp://hdl.handle.net/10400.4/728
dc.language.isoporpt
dc.publisherSociedade Portuguesa de Obstetrícia e Ginecologiapt
dc.subjectNeoplasias do Ováriopt
dc.subjectTumor de Células de Leydigpt
dc.titleTumor de células de Leydig do ovário: caso clínicopt
dc.title.alternativeLeyding cell tumour of the ovary: a case reportpt
dc.typejournal article
dspace.entity.typePublication
rcaap.rightsopenAccesspt
rcaap.typearticlept

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