Iranian Journal of Reproductive Medicine
Research and Clinical Center for Infertility, Shahid Sadoughi University of Medical Sciences of Yazd
Vol. 14, No. 3, 2016, pp. 213-216
Bioline Code: rm16028
Full paper language: English
Document type: Case Report
Document available free of charge
Iranian Journal of Reproductive Medicine, Vol. 14, No. 3, 2016, pp. 213-216
© Copyright 2016 - Iranian Journal of Reproductive Medicine
Congenital adrenal hyperplasia and vanishing testis: rare case of male pseudohermaphroditism|
Ghanei, Azam; Mohammadzade, Golnaz; Zarepur, Ehsan & Soheilikhah, Sedigheh
Background: Congenital adrenal hyperplasia (CAH) and vanishing testes are uncommon diseases that can result from hormonal and mechanical factors. Classic CAH is determined by ambiguous genitalia and increase in amount of 17-Hydroxyprogesterone. Simultaneous occurrence of CAH and vanishing testes is a rare condition.
Case:A 22-year-old boy, known case of CAH who was diagnosed as female
pseudohermaphroditism due to ambiguous genitalia, was referred to Shahid
Sadoughi Hospital, Yazd, Iran with colicky abdominal pain and hematuria.
Ultrasonography has been performed and prostate tissue was reported. Karyotyping
was done because of uncertainty in primary diagnosis, which revealed 46XY. For
finding location of testes, ultrasonography and MRI were done and nothing was
found in abdomen, inguinal canal or scrotum. Inhibin B serum level was measured
to find out whether testis tissue was present in the body, which was <1 pg/ml and
vanishing testis was confirmed.
Conclusion: Early diagnosis and treatment are essential to prevent further sequels and karyotyping for all patients with CAH is recommended. Lifelong treatment with synthetic glucocorticoid replacement is necessary.
Congenital adrenal hyperplasia; Vanishing testes; Ambiguous genitalia
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