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British Journal of Radiology (2008) 81, e176-e178
© 2008 British Institute of Radiology
doi: 10.1259/bjr/76916885
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Case report

Transverse testicular ectopia associated with persistent Müllerian duct syndrome — the role of imaging

A A GUTTE, MD, DNB1, P S PENDHARKAR, MD, DMRD2 and S Z SORTE, MD1

1 Department of Radiology, GMC & Sir JJ group of Hospitals, Mumbai, 2 Department of Radiology, Jawarharlal Nehru Medical College, Wardha, Maharashtra, India

Correspondence: Dr Avinash A Gutte, Department of Radiology, GMC & Sir JJ group of Hospitals, Byculla, Mumbai, Maharashtra 400008, India. E-mail: avinash_gutte{at}yahoo.com

Persistent Müllerian duct syndrome (PMDS) is a rare form of male pseudohermaphroditism, characterized by the presence of a uterus and fallopian tubes owing to failure of Müllerian duct regression in genotypically normal males. More than 150 cases have been recorded, most of them in adults. The association between a persistent Müllerian duct and transverse testicular ectopia is even more uncommon. We report a case of a male infant diagnosed transverse testicular ectopia with PMDS.






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