Diagnosis of pseudohermaphroditism (gonads and secondary characteristics of the opposite sex) after puberty is rare. We observed a mis-diagnosed case of pseudohermaphroditism caused by the persistence of Mullerian ducts (vagina, uterus and Fallopian tubes) in a 72-year-old patient, who had previously undergone several operations for urethral stenosis and bilateral criptorchidism.
SuotoC.A.V.Da Costa OliveriraM.TelokenC.PaskulinG.HoffmannK.: Persistence of mullerian duct derivative syndrome in 2 male patients with bilateral cryptorchidism. J. Urol., 153: 1637–1638, 1995.
2.
MartinL.E.BennetA.H.CromieW.J.: Persistent mullerian duct syndrome with transverse testicular ectopia and spermatogenesis. J. Urol., 147: 1615–1617, 1992.
3.
BorerJ.G.NittiV.W.GlassbergK.I.: Mixed gonodal dysgenesis and dysgenetic male pseudohermaphroditism. J. Urol., 153: 1267–273, 1995.
4.
YuT.J.ShuK.RungF.T.EngH.L.ChenH.Y.: Use of laparoscopy in intersex patients. J. Urol., 154: 1193–1196, 1995.
