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A Female Infant with Segmental Multicystic Dysplastic Kidney
Journal of the Korean Society of Pediatric Nephrology ; : 25-28, 2013.
Artículo en Inglés | WPRIM | ID: wpr-51011
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.
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Texto completo: Disponible Índice: WPRIM (Pacífico Occidental) Asunto principal: Biopsia / Historia Natural / Riñón Displástico Multiquístico Límite: Adulto / Femenino / Humanos / Lactante Idioma: Inglés Revista: Journal of the Korean Society of Pediatric Nephrology Año: 2013 Tipo del documento: Artículo

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Texto completo: Disponible Índice: WPRIM (Pacífico Occidental) Asunto principal: Biopsia / Historia Natural / Riñón Displástico Multiquístico Límite: Adulto / Femenino / Humanos / Lactante Idioma: Inglés Revista: Journal of the Korean Society of Pediatric Nephrology Año: 2013 Tipo del documento: Artículo