J Korean Soc Pediatr Nephrol.  2013 Apr;17(1):25-28.

A Female Infant with Segmental Multicystic Dysplastic Kidney

Affiliations
  • 1Department of Pediatrics, CHA Bundang Medical Center, CHA University, Seongnam, South Korea. naesusana@yahoo.co.kr

Abstract

There have only been 35 pediatric cases and one adult case reported on segmental multicystic dysplastic kidney (MCDK) from our search in PubMed, including 19 cases detected antenatally. There is little documentation of segmental MCDK, particularly concerning its natural history. Segmental MCDK can be presented atypically, making diagnosis more difficult. We report an another case with segmental MCDK. Multicystic abdominal mass detected on antenatal sonogram in this infant was diagnosed as segmental MCDK by renal ultrasonography and computed tomography. If a definitive diagnosis of segmental MCDK can be made on imaging, surgery is not required for a diagnostic biopsy.

Keyword

Computed tomography; Multicystic renal mass; Renal ultrasonography; Segmental multicystic dysplastic kidney

MeSH Terms

Adult
Biopsy
Female
Humans
Infant
Multicystic Dysplastic Kidney
Natural History
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