Pure Ovarian Leydig Cell Tumors

Authors

  • Antônio Chambô Filho Ph.D Gineco-obstetra, Chefe da Residência Médica em Ginecologia e Obstetrícia da Santa Casa de Misericórdia de Vitória (SCMV)
  • Eduardo F Scárdua M.Sc Ginecologia e Obstetrícia e Professor Assistente de Ginecologia da SCMV
  • Luis C Cintra Médico Patologista da SCMV
  • Tatiana C Guzzo Médica Ginecologista e Obstetra da SCMV
  • Thiago Martinelli Médico Ginecologista e Obstetra da SCMV
  • Luziany D Gonçalves Médica-residente em Ginecologia e Obstetrícia da SCMV
  • Daniela Pratti Médica-residente em Ginecologia e Obstetrícia da SCMV

DOI:

https://doi.org/10.32635/2176-9745.RBC.2008v54n3.1722

Keywords:

Leydig cell tumors, Ovarian neoplasms, Hyperandrogenism, Virilism

Abstract

Pure Leydig cell tumors are rare ovarian steroid cell neoplasms composed entirely or predominantly of Leydig cells. More than 75% of patients present signs of virilization due to overproduction of testosterone. We report the clinical manifestations, diagnosis, and treatment of a case of pure Leydig cell tumor at the Gynecology Department of Santa Casa de Misericórdia (Mercy Hospital) in Vitória, Espírito Santo State, Brazil, in 2002. The case was a 47-year-old female with progressive signs of virilization for more than five years. Laboratory examination revealed only high levels of serum testosterone. There was no evidence of alteration in adrenal glands during diagnostic imaging. Transvaginal ultrasound showed only a slightly enlarged right ovary, with no radiological sign of tumor. Total hysterectomy and bilateral salpingoophorectomy were performed. Histopathology and immunohistochemistry confirmed the diagnosis of pure Leydig cell tumor. After surgery, testosterone level returned to normal and there was no significant evidence of virilization.

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Published

2008-09-30

How to Cite

1.
Chambô Filho A, Scárdua EF, Cintra LC, Guzzo TC, Martinelli T, Gonçalves LD, Pratti D. Pure Ovarian Leydig Cell Tumors. Rev. Bras. Cancerol. [Internet]. 2008 Sep. 30 [cited 2024 May 18];54(3):245-50. Available from: https://rbc.inca.gov.br/index.php/revista/article/view/1722

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Section

CASE REPORT

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