Caliceal diverticulum with ureteropelvic junction obstruction in a dysplastic kidney: a pediatric case report.
Caliceal diverticulum
Child
Dysplastic kidney
Etiology
Ureteropelvic junction obstruction
Journal
CEN case reports
ISSN: 2192-4449
Titre abrégé: CEN Case Rep
Pays: Japan
ID NLM: 101636244
Informations de publication
Date de publication:
08 2021
08 2021
Historique:
received:
12
08
2020
accepted:
14
12
2020
pubmed:
9
1
2021
medline:
25
11
2021
entrez:
8
1
2021
Statut:
ppublish
Résumé
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.
Identifiants
pubmed: 33417184
doi: 10.1007/s13730-020-00569-4
pii: 10.1007/s13730-020-00569-4
pmc: PMC8271042
doi:
Types de publication
Case Reports
Langues
eng
Sous-ensembles de citation
IM
Pagination
332-335Informations de copyright
© 2021. Japanese Society of Nephrology.
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