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

AbstractOBJECTIVES:
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.
AuthorsJ Calleja Escudero, A Amo García, M Garrido Redondo, A Rodríguez Toves, F del Río Domínguez, J M Martínez Sagarra
JournalArchivos espanoles de urologia (Arch Esp Urol) Vol. 48 Issue 1 Pg. 89-91 ( 1995) ISSN: 0004-0614 [Print] Spain
Vernacular TitleAgenesia renal, uréter ciego craneal y ureterocele. A propósito de un caso.
PMID7733696 (Publication Type: Case Reports, English Abstract, Journal Article)
Topics
  • Abnormalities, Multiple (diagnosis)
  • Adolescent
  • Humans
  • Kidney (abnormalities)
  • Male
  • Ureter (abnormalities)
  • Ureterocele (complications)

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