A Female Infant with Segmental Multicystic Dysplastic Kidney
Journal of the Korean Society of Pediatric Nephrology
; : 25-28, 2013.
Article
en En
| WPRIM
| ID: wpr-51011
Biblioteca responsable:
WPRO
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.
Palabras clave
Texto completo:
1
Base de datos:
WPRIM
Asunto principal:
Biopsia
/
Historia Natural
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Riñón Displástico Multiquístico
Límite:
Adult
/
Female
/
Humans
/
Infant
Idioma:
En
Revista:
Journal of the Korean Society of Pediatric Nephrology
Año:
2013
Tipo del documento:
Article