A rare case of renal dysplasia: prenatal and postnatal management

Giuseppe Noia, Daniela Visconti, Luisa D'Oria, Marcella Pellegrino, Concetta Leggieri, Carlo Manzoni, Lucia Masini, Alessandro Caruso

Research output: Contribution to journalArticlepeer-review

Abstract

The ultrasonographic detection of renal anomalies may modify obstetric management and facilitate pediatric care of the newborn. We performed prenatal differential diagnosis of an isolated unilateral cystic renal mass (71 × 74 × 82 mm) in a pregnant woman at 26 weeks of gestation. No other abnormalities were detected by ultrasonography, except for polyhydramnios. Repeated percutaneous cyst aspirations were required because of the increasing risk of vital organ damage. Postnatal nephroureterectomy was performed. Anatomopathologic analysis led to the diagnosis of segmental renal dysplasia, which could not be included in any of the four groups of Potter's classification of cystic renal dysplasia.
Original languageEnglish
Pages (from-to)437-442
Number of pages6
JournalFetal and Pediatric Pathology
Volume32
DOIs
Publication statusPublished - 2013

Keywords

  • renal dysplasia

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