A rare case of renal dysplasia: prenatal and postnatal management

Lucia Masini, Giuseppe Noia, Daniela Visconti, Marcella Pellegrino, Carlo Manzoni, Alessandro Caruso

Risultato della ricerca: Contributo in rivistaArticolo in rivista

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 4 groups of Potter’s classification of cystic renal dysplasia
Lingua originaleEnglish
pagine (da-a)437-442
Numero di pagine6
RivistaFetal and Pediatric Pathology
Volume32
DOI
Stato di pubblicazionePubblicato - 2013

Keywords

  • diagnosi prenatale
  • displasia renale fetale
  • fetal renal dysplasia
  • prenatal diagnosis

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