Caliceal diverticulum with ureteropelvic junction obstruction in a dysplastic kidney: a pediatric case report View Full Text


Ontology type: schema:ScholarlyArticle      Open Access: True


Article Info

DATE

2021-01-08

AUTHORS

Keiichi Koizumi, Noboru Oyachi, Fuminori Numano, Takahiko Mitsui

ABSTRACT

A caliceal diverticulum is a rare entity in children. Its etiology is closely associated with that of ureteropelvic junction malformations and renal dysplasia. We herein present a case of these complex disorders in an infant. A renal cyst and hydronephrosis were found in the left kidney during the fetal period. The postnatal diagnosis was hydronephrosis due to ureteropelvic junction obstruction and a caliceal diverticulum in the left dysplastic kidney. Although left renal function was severely decreased, the patient had no symptoms. Therefore, we did not perform surgical treatment. At the time of this writing, the patient was 3 years 8 months old and had developed no symptoms. More... »

PAGES

332-335

Identifiers

URI

http://scigraph.springernature.com/pub.10.1007/s13730-020-00569-4

DOI

http://dx.doi.org/10.1007/s13730-020-00569-4

DIMENSIONS

https://app.dimensions.ai/details/publication/pub.1134448481

PUBMED

https://www.ncbi.nlm.nih.gov/pubmed/33417184


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