IMR Press / CEOG / Volume 35 / Issue 2 / pii/1630638490555-448106196

Clinical and Experimental Obstetrics & Gynecology (CEOG) is published by IMR Press from Volume 46 Issue 1 (2019). Previous articles were published by another publisher on a subscription basis, and they are hosted by IMR Press on imrpress.com as a courtesy and upon agreement with S.O.G.

Open Access Case Report
Mucinous cystadenoma in a female patient with 45,X/46,XY karyotype
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1 Department of Medical Genetics, Baskent University Faculty of Medicine, Ankara
2 Department of Obstetrics and Gynecology, Baskent University Faculty of Medicine, Ankara
3 Department of Pathology, Baskent University Faculty of Medicine, Ankara (Turkey)
Clin. Exp. Obstet. Gynecol. 2008, 35(2), 144–146;
Published: 10 June 2008
Abstract

The mosaic karyotype of 45,X/46,XY has a wide phenotypic spectrum and there are substantial differences between prenatally and postnatally diagnosed cases. The phenotype varies between normal male to classical Turner syndrome. There is a high risk of gonadal tumor development in the dysgenetic gonads of patients with sex chromosome mosaicism. We report a case of a 24-year-old patient with a pelvic mass and amenorrhea referred to our laboratory for karyotyping. Peripheral blood chromosome analysis showed a mosaic karyotype of 45,X[17]/46,XY[83]. The tumor originated from the left ovary and the right ovary was found to be a streak gonad. The uterus was intact. Pathologic examination of the tumor revealed mucinous cystadenoma. Physical examination of the patient showed signs of Turner syndrome, as short stature (145 cm), short neck and asymmetric shoulders. Her mental state was normal. Y chromosome microdeletion screening involving SRY and ZFY genes was performed and no deletion was found. The patient was informed about the condition during the genetic counseling session.
Keywords
Mucinous cystadenoma
Chromosomal mosaicism
Turner syndrome
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