Familial Renal Agenesis and Urogenital Malformations

Seminal Vesicle Cyst and Vaginal Cyst with Bicornnuate Uterus in Siblings

Jens B. KnudsenDepartments of Surgery, Radiology and Pathology, Fredrikshorg Amt Centralsygehus, Hillerød, Denmark

Birgitte BrunDepartments of Surgery, Radiology and Pathology, Fredrikshorg Amt Centralsygehus, Hillerød, Denmark

Hans Chr. EmusDepartments of Surgery, Radiology and Pathology, Fredrikshorg Amt Centralsygehus, Hillerød, Denmark

Abstract

A seminal vesicle cyst was found in a 38-year-old man with ipsilateral renal agenesis. His sister had embryologically analogous malformations—Gartner duct cyst, bicornuate uterus and renal agenesis. This seems to be the first reported familial occurrence of these combined malformations. The embryogenesis is reviewed and the diagnostic procedure and treatment are discussed.

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Familial Renal Agenesis and Urogenital Malformations

Seminal Vesicle Cyst and Vaginal Cyst with Bicornnuate Uterus in Siblings

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Familial Renal Agenesis and Urogenital Malformations

Seminal Vesicle Cyst and Vaginal Cyst with Bicornnuate Uterus in Siblings

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