Literature DB >> 21084958

Prenatal diagnosis of renal developmental anomalies associated with an empty renal fossa.

Karen Y Oh1, David Edward Holznagel, Jonathan R Ameli, Roya Sohaey.   

Abstract

Fetal kidneys are evaluated on routine obstetric ultrasounds; therefore, fetal renal developmental anomalies are frequently encountered with prenatal screening. Absence of the fetal kidney from its expected location generates a differential diagnosis that originates from the knowledge of the developmental origins of the kidneys. Many of the renal developmental anomalies demonstrate overlapping features in both symptoms and imaging appearance. We illustrate the pertinent findings of selected fetal renal anomalies in the setting of a unilateral empty renal fossa and suggest an algorithm for differentiating between the diagnoses. Discussed anomalies include horseshoe kidney, pelvic kidney, crossed fused renal ectopia, and renal agenesis.

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Year:  2010        PMID: 21084958     DOI: 10.1097/RUQ.0b013e3181f573fd

Source DB:  PubMed          Journal:  Ultrasound Q        ISSN: 0894-8771            Impact factor:   1.657


  2 in total

Review 1.  Life with one kidney.

Authors:  Michiel F Schreuder
Journal:  Pediatr Nephrol       Date:  2017-05-29       Impact factor: 3.714

Review 2.  Management of the congenital solitary kidney: consensus recommendations of the Italian Society of Pediatric Nephrology.

Authors:  Claudio La Scola; Anita Ammenti; Cristina Bertulli; Monica Bodria; Milena Brugnara; Roberta Camilla; Valentina Capone; Luca Casadio; Roberto Chimenz; Maria L Conte; Ester Conversano; Ciro Corrado; Stefano Guarino; Ilaria Luongo; Martino Marsciani; Pierluigi Marzuillo; Davide Meneghesso; Marco Pennesi; Fabrizio Pugliese; Sara Pusceddu; Elisa Ravaioli; Francesca Taroni; Gianluca Vergine; Licia Peruzzi; Giovanni Montini
Journal:  Pediatr Nephrol       Date:  2022-06-17       Impact factor: 3.651

  2 in total

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