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[Renal agenesis, cranial blind ureter and ureterocele. Report of a case].

作者信息

Calleja Escudero J, Amo García A, Garrido Redondo M, Rodríguez Toves A, del Río Domínguez F, Martínez Sagarra J M

机构信息

Servicio de Urología, Hospital del Rio Hortega, Valladolid, España.

出版信息

Arch Esp Urol. 1995 Jan-Feb;48(1):89-91.

PMID:7733696
Abstract

OBJECTIVES

We report a case of associated malformations in a young male with recurrent epididymitis.

METHODS

In our study we used the following techniques: ultrasound, intravenous urography, retrograde pyelography, computed tomography and cystoscopy.

RESULTS

We observed three coexisting congenital malformations: renal agenesis, cranial blind-ending ureter and ureterocele.

CONCLUSIONS

Different urologic malformations are usually found in association. In our view only symptomatic ureteroceles require treatment.

摘要

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Arch Esp Urol. 1995 Jan-Feb;48(1):89-91.
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