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[Association of a rare form of testicular ectopia, a persistent Müllerian duct syndrome and a supernumerary ectopic epididymis].

作者信息

Giannopoulos A, Pantazopoulos D, Michalopoulos A, Goulandris N, Dimopoulos C

出版信息

Ann Urol (Paris). 1986;20(4):267-70.

PMID:3740807
Abstract

We report the first case of persistence of the Müllerian duct associated with transverse testicular ectopia and a supernumerary ectopic epididymis in the same hemiscrotum. The patient is a thirty-year-old man with azoospermia. Uterine and Fallopian tube structures were clearly recognizable within the Müllerian remnants. The ectopic supernumerary epididymis was detected at the lower pole of one of the two testicles and had to be removed surgically.

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